Next Article in Journal
Osteoporosis Due to Hormone Imbalance: An Overview of the Effects of Estrogen Deficiency and Glucocorticoid Overuse on Bone Turnover
Next Article in Special Issue
Systemic Lectin-Glycan Interaction of Pathogenic Enteric Bacteria in the Gastrointestinal Tract
Previous Article in Journal
Nischarin Deletion Reduces Oxidative Metabolism and Overall ATP: A Study Using a Novel NISCHΔ5-6 Knockout Mouse Model
Previous Article in Special Issue
Computer Modeling Explains the Structural Reasons for the Difference in Reactivity of Amine Transaminases Regarding Prochiral Methylketones
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 23
Issue 3
10.3390/ijms23031375
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

IKKα Induces Epithelial–Mesenchymal Changes in Mouse Skin Carcinoma Cells That Can Be Partially Reversed by Apigenin

by
Verónica A. García-García
1,2,†,
Josefa P. Alameda
1,2,3,†,
Angustias Page
1,2,3,
Antonio Mérida-García
1,4,
Manuel Navarro
1,2,3,
Adrián Tejero
1,
Jesús M. Paramio
1,2,3,
Rosa A. García-Fernández
5 and
M. Llanos Casanova
1,2,3,*
1
Molecular and Translational Oncology Unit, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), 28040 Madrid, Spain
2
Biomedical Research Institute I+12, 12 de Octubre University Hospital, 28040 Madrid, Spain
3
Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), 28029 Madrid, Spain
4
Complejo Asistencial de Zamora, 49022 Zamora, Spain
5
Department of Animal Medicine and Surgery, Facultad de Veterinaria, Complutense University of Madrid (UCM), 28040 Madrid, Spain
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2022, 23(3), 1375; https://doi.org/10.3390/ijms23031375
Submission received: 20 December 2021 / Revised: 21 January 2022 / Accepted: 21 January 2022 / Published: 25 January 2022
(This article belongs to the Special Issue 23rd Anniversary of IJMS: Advances in Biochemistry)
Browse Figures
Versions Notes

Abstract

:
NMSC (non-melanoma skin cancer) is a common tumor in the Caucasian population, accounting for 90% of skin cancers. Among them, squamous cell carcinomas (SCCs) can metastasize and, due to its high incidence, constitute a severe health problem. It has been suggested that cutaneous SCCs with more risk to metastasize express high levels of nuclear IKKα. However, the molecular mechanisms that lead to this enhanced aggressiveness are largely unknown. To understand in depth the influence of nuclear IKKα in skin SCC progression, we have generated murine PDVC57 skin carcinoma cells expressing exogenous IKKα either in the nucleus or in the cytoplasm to further distinguish the tumor properties of IKKα in both localizations. Our results show that IKKα promotes changes in both subcellular compartments, resembling EMT (epithelial–mesenchymal transition), which are more pronounced when IKKα is in the nucleus of these tumor cells. These EMT-related changes include a shift toward a migratory phenotype and induction of the expression of proteins involved in cell matrix degradation, cell survival and resistance to apoptosis. Additionally, we have found that apigenin, a flavonoid with anti-cancer properties, inhibits the expression of IKKα and attenuates most of the pro-tumoral EMT changes induced by IKKα in mouse tumor keratinocytes. Nevertheless, we have found that apigenin only inhibits the expression of the IKKα protein when it is localized in the cytoplasm.

1. Introduction

NMSC is the most common human neoplasm in the Caucasian population, accounting for 90% of skin cancers; moreover, the incidence of both benign and malignant NMSC has been increasing at an alarming rate in recent years, including in the population younger than 40 years [1], making NMSC an important health problem.
NMSC includes two different entities: BCCs (basal cell carcinomas) and SCCs; while BCCs rarely metastasize, metastasis from high-risk SCC are more frequent and may be lethal. Almost 5% of SCCs metastasize; therefore, due to its high incidence, the mortality concomitant to aggressive cutaneous SCCs is reaching important numbers [2]. Furthermore, the risk for developing skin SCCs highly increases in several conditions, i.e., almost all patients suffering from recessive dystrophic epidermolysis bullosa (RDEB) are prone to develop aggressive and metastatic skin SCCs at early ages [3]; in addition, organ transplant recipients have a higher risk to develop skin SCCs (65–250 times compared with the general population) that in addition are more aggressive [4]. This makes the elucidation of the molecular changes that lead to aggressive skin SCCs an urgent matter. In this regard, it has been reported that the nuclear localization of IKKα (inhibitor of nuclear factor kappa-B kinase subunit alpha) is a hallmark of aggressive human cutaneous SCCs with a high risk to metastasize [5]. However, despite these data, the mechanisms through which IKKα favors cutaneous SCCs aggressiveness have not been fully unveiled.
In the cytoplasm, IKKα is part of the IKK complex that regulates the NF-κB transcription factor [6]. It is considered that its main function is the regulation of epidermal differentiation, since IKKα-deficient mice exhibit marked morphological abnormalities that include taut and shiny skin that is unable to differentiate, and they lack a barrier function; as a consequence, IKKα-null mice die shortly after birth by dehydration [7,8]. In addition to its cytoplasmic functions, nuclear roles for IKKα have been identified [9,10,11]; thus, it was reported that it regulated the epidermal differentiation in the nucleus, independent of the NF-κB pathway and through the modulation of the EGFR and Smads pathways [12,13,14]. Therefore, due to its key role in skin morphogenesis, it is not surprising that IKKα was also involved in NMSC development and progression [5,15,16,17,18]. Furthermore, our group has recently described that IKKα may act in both subcellular localizations, in the nucleus and in the cytoplasm of keratinocytes, as a promoter of skin SCC aggressiveness [15].
A well-recognized mechanism that promotes cancer progression and malignancy is the EMT process, since it enhances the invasive properties of cancer cells, including epidermal cells [19,20]. EMT causes the reprogramming and phenotypic changes through which immobile cancer epithelial cells acquire a migratory mesenchymal phenotype and repress the expression of epithelial markers such as keratins, while inducing those characteristics of mesenchymal cells, such as Vimentin [21,22]. According to these changes, EMT is accompanied by the induction of the expression of metalloproteases, such as MMP9, that can degrade the basement membrane, thereby favoring cell migration and invasion [23]. Notably, the EMT process not only induces increased cancer cell motility and invasiveness but also allows cancer cells to avoid anoikis and cellular senescence while favoring cell survival [24,25]. Furthermore, it has been suggested that EMT facilitates the acquisition of resistance to apoptosis, a key characteristic required for tumor survival [25], which is mainly mediated by Snail1, a master regulator of EMT [26,27]. Moreover, EMT plays a role not only in tumor progression, but also in the metastatic cascade of many solid tumors, representing a hallmark of this event [28]. EMT is also implicated in tumor resistance to chemotherapy and radiotherapy [28,29].
In the case of NMSC, there is evidence of EMT involvement in the progression of actinic keratosis to invasive cutaneous SCC [30]. EMT activation has also been found in invasive skin SCCs compared to normal skin and with SCCs in situ [31]. Therefore, given that EMT and nuclear expression of IKKα are two factors that favor the greater aggressiveness of skin SSCs [5], in this work, we have studied whether nuclear IKKα induces EMT in epidermal cancer cells. For this purpose, we have generated PDVC57 skin carcinoma cells that constitutively express increased levels of IKKα in the nucleus or in the cytoplasm (named as C57-N-IKKα and C57-C-IKKα cells respectively). Our results show that both types of PDVC57 cells that express ectopic IKKα acquire a high capacity of migration and induce the expression of MMP9 and the survival proteins Bcl2 and Akt, while repressing the expression of proapoptotic proteins. These changes suggest that IKKα favors the EMT process in tumor epidermal cells. This effect is particularly marked in the C57-N-IKKα cells, which in addition, switch their epithelial morphology toward a fibroblastoid phenotype, induce the expression of Snail1, and repress that of keratin 5 (K5).
Additionally, and given that the finding of an efficient treatment for aggressive skin SCCs is a critical issue, we have tested the possible utility of apigenin as a potential anti-skin SCC treatment. Apigenin is a bioactive flavonoid with anticancer activity in many types of cancers whose action is mediated by different mechanisms [32]. In the case of prostate cancer, it was shown that apigenin exerted its antitumor effect through direct interaction with IKKα [33,34]. Although it has been shown that apigenin also acts as an antitumor agent in NMSC [35,36], its mechanisms of action remain largely unknown, and the possible involvement of IKKα in the anticancer activity of apigenin in skin SCCs has not been addressed yet. Thus, we have carried out this study and found that apigenin inhibits the expression of the IKKα protein, as well as the EMT changes induced by IKKα in the C57 cells, at low concentrations and at early time points of treatment, but only when IKKα is localized in the cytoplasm of keratinocytes.

2. Results

2.1. Exogenous Expression of IKKα in the Nucleus or Cytoplasm of PDVC57 Skin Carcinoma Cells

We have generated transfectant cells which express an exogenous human IKKα protein specifically in the cytoplasmic or nuclear compartment of the PDVC57 cell line (designated as C57-C-IKKα and C57-N-IKKα cells, respectively). PDVC57 mouse skin carcinoma cells were chosen because they bear the Ha-ras mutation carried by most of the chemically induced mouse skin tumors and some human skin carcinomas [37,38,39,40]. PDVC57 cells were stably transfected with the human IKKα complementary DNA under the control of the β-actin promoter, which lacks the nuclear localization signal (NLS) in the C-IKKα construct or which carries an extra NLS in the N-IKKα construct, and both of them tagged with a Flag epitope (Figure 1A) or with the empty vector [15]. Pooled of stable transfectants from approximately 50 different G418-resistant colonies were used to minimize any potential effect of clonal selection. Results from C57-C-IKKα and C57-N-IKKα cells were compared with that of C57-Control cells (which carry the empty vector). Western blot showed that C57-C-IKKα and C57-N-IKKα cells express the transgene, which is slightly larger due to the tag (Figure 1A). Next, we performed immunofluorescence staining to check in situ the expression of the transgene (Figure 1B–H). We found that C57-C-IKKα (Figure 1C–E) and C57-N-IKKα cells (Figure 1F–H) expressed the transgene in the cytoplasm and in the nucleus, respectively. For the following experiments, we chose two clones of each genotype which expressed different levels (low or high) of the transgene; therefore, clones N3 and N4 carrying the N-IKKα construct and clones C4 and C8, bearing the C-IKKα construct were selected; in the case of Control cells, clones Control1 and Control2 were chosen for studies.

2.2. Increased Migratory Capacity of Both C57-C-IKKα and C57-N-IKKα Cells in Culture

We observed that the expression of IKKα in the nucleus of C57-N-IKKα cells confers them an enlarged and elongated shape that reminds that of fibroblasts (Figure 2). Therefore, we performed colony-forming assays to better analyze the shape of the colonies formed by the three types of cells and found that, in contrast with the rounded and dense colonies with a well-defined shape formed by C57-Control cells (Figure 3A,B), those formed by C57-N-IKKα cells appeared large, loose and showed an imprecise contour, with cells that did not compact and did not acquire the classic rounded form characteristic of cell colonies (Figure 3C–E); in contrast, colonies of C57-C-IKKα cells usually had a phenotype similar to that of C57-Control cells (Figure 3F), although colonies of an intermediate phenotype between that of C57-Control and C57-N-IKKα cells were sometimes perceived (Figure 3G,H). When observed at higher magnification, the presence of groups of cells migrating from the C57-N-IKKα colonies (Figure 3J) is observed; these groups of cells were also detected in the C57-C-IKKα colonies, although they were less frequent (Figure 3K).
Next, the effect of nuclear and cytoplasmic IKKα expression on C57 cell motility was analyzed in in vitro wound healing assays: cells growing in monolayer cultures were subjected to scratch wounds and found that at 48 h post-scratching both C57-C-and-N-IKKα cells formed frequent peaks of migration, (Figure 4E–L); by contrast, in the scratch wound of the C57-Control cells, only a few migratory cells were observed (Figure 4A–D). Additionally, both C57-N-and-C-IKKα cells achieved greater migration distance (Figure 4E–L). Therefore, our results suggest that increased levels of IKKα lead to an enhancement of the capacity of migration of tumor epidermal cells, and importantly, similar results were obtained from the analysis of clones that express low or high levels of ectopic IKKα, suggesting that it is sufficient a small increment in the expression level of IKKα to induce the indicated changes (Figure 3 and Figure 4).

2.3. Induction of Snail and Vimentin Expression and Inhibition of K5 in C57-N-IKKα Cells

The fibroblastoid phenotype of C57-N-IKKα cells together with their increased migratory ability suggest that they were undergoing a process of EMT; therefore, we analyzed the expression of the master gene of EMT, Snail1, and found that it was highly induced in C57-N-IKKα cells compared with C57-Control cells, while only a slight increase in the expression of Snail1 (not statistically significant) was detected in the C57-C-IKKα cells (Figure 5A). Another feature of EMT is a switch of the expression of epithelial markers toward mesenchymal ones; therefore, we analyzed the expression of Vimentin and found that it was increased in C57-N-IKKα cells (Figure 5B), which correlated with the morphological change observed in the shape of these cells. Next, we examined the expression of the keratin K5 in the three types of C57-cells, since the downregulation of the expression of keratins in epithelial cells is a well-established biomarker of EMT [41]. We found that the expression of K5 was inhibited in the C57-N-IKKα cells: it was observed that those cells expressing the ectopic IKKα did not express K5 (Figure 5D); thus, we only detected K5 expression in the minority of cells, which do not express the ectopic nuclear IKKα (arrow in Figure 5D). By contrast, co-expression of both K5 and IKKα was detected in both C57-Control and C57-C-IKKα cells (Figure 5C,E).
Another change that occurs during the EMT process is the induction of the expression of metalloproteases that can degrade the basement membrane, thereby favoring cell migration and invasion. We analyzed MMP9 expression and saw that it was induced in both C57-C-IKKα and C57-N-IKKα cells (Figure 6A), which is consistent with the increased migratory capacity of both types of cells (Figure 4). To determine the source of MMP9 production, we analyzed the expression of c-Myc since it has been reported that Myc induces MMP9 [42], and c-Myc overexpression is involved in EMT during transformation of different epithelial cells [43]. The analysis by WB showed increased levels of c-Myc in the C57-N-IKKα cells and a slight induction in the C57-C-IKKα ones (Figure 6B). These results agree with our previous results, which showed the induction of c-Myc both in skin carcinomas developed by chemical skin carcinogenesis in K5-N-IKKα transgenic mice [15] and in the N-H460-IKKα lung adenocarcinoma cells [44].
We confirmed these results in another cell line, the mouse tumor keratinocyte PB cell line [45] (Supplementary Figure S1). PB cells were transfected with the C-or-N-IKKα constructs (or with the empty vector), and it was obtained three pooled stable transfectans clones from 25–40 different colonies, named as PB-C-IKKα, PB-N-IKKα and PB-Control clones. The correct expression of the transgene in the nucleus of PB-N-IKKα cells and in the cytoplasm of the PB-C-IKKα cells was determined by immunofluorescence analysis (Figure S1A–C). Western blot analysis confirmed the expression of the exogenous human IKKα in the transfected PB-C-and-N-IKKα cells (Figure S1D). Similar to the data obtained with the C57 cells, we observed that both PB-C-and-N-IKKα cells expressed increased levels of MMP9 and c-Myc; additionally, it was found that the expression of K5 was inhibited in the PB-N-IKKα cells, since similar to the staining in the C57-N-IKKα cells, those cells expressing the ectopic IKKα did not express K5 (asterisks in Figure S1E), while K5 expression was observed in the cells which do not express the ectopic nuclear IKKα (arrows in Figure S1E). Likewise, equal to the staining observed in C57-C-IKKα cells, co-expression of both K5 and IKKα was detected in PB-C-IKKα cells (Figure S1F). Therefore, these results suggest that the changes in both C57 and PB-C-and-N-IKKα tumor keratinocytes are likely due to augmented IKKα expression in each subcellular localization of skin carcinoma cells.

2.4. C57-N-IKKα Cells Have Increased Survival Capacity

Another characteristic of the cells that experiment an EMT process is the increase in their survival capacity as well as in their apoptotic resistance. Thus, we tested the behavior of the C57 cells of the three genotypes in a situation of stress such as culture in the absence of serum. It was observed that both C57-C-IKKα and C57-N-IKKα cells had an increased capacity to survive in absence of FBS, being the number of cells that persisted after 7 days of culture in the absence of FBS higher in the C57 cells expressing the exogenous IKKα in each subcellular localization (Figure 7A–D). In agreement with this observation, we analyzed the levels of expression of Akt, a protein known to increase the survival of cancer cells [46] and found that it was induced in both types of C57-IKKα cells (Figure 7E), while a lower than control amount of the proapoptotic cleaved-Caspase 3 was detected in both C57-C-IKKα and C57-N-IKKα cells (Figure 7E). Next, we analyzed the expression of the anti-apoptotic and pro-survival protein Bcl-2 and found that its expression was also increased in both types of C57-IKKα cells, mainly in the C57-N-IKKα cells (Figure 7E). Therefore, our results show that the increased levels of IKKα in the C57 skin carcinoma cells confers them a greater capacity for survival and resistance to apoptosis in stressful situations, such as culture in the absence of serum.

2.5. Apigenin Inhibits the Expression of the IKKα Protein in the Cytoplasm but Not in the Nucleus of C57 Cells

The capacity of apigenin to inhibit NMSC has been reported [35,36]; however, its mechanisms of action remain largely unknown. In particular, whether apigenin has an effect on IKKα expression has not been studied yet. Therefore, we proceeded to analyze this. First, we performed cell viability assays of cells growing in the absence or presence of apigenin at two different concentrations, 10 and 20 µM, which are the concentrations reported in different types of tumors, including in NMSC [35,36,47], for different periods (24–72 h). Then, 10 µM apigenin resulted in only a slight reduction in the number of cells in the three types of C57 clones at 72 h (Figure 8A). However, when cells were grown in the presence of apigenin 20 µM, a significant reduction in the number of cells was detected from 48 h of culture and even more at 72 h (Figure 8B). Then, we explored whether, as reported in prostate cancer cells [33], apigenin regulates IKKα in skin cancer cells. We analyzed by WB the possible influence of apigenin treatment in the expression levels of IKKα in the C57 cells of the three genotypes. Our results showed that treatment with 10–40 µM of apigenin during 48 h was enough to diminish the expression of endogenous mouse IKKα in the three types of C57 cells (Figure 9A,B); at this time point, apigenin also reduced the levels of the exogenous cytoplasmic IKKα in the C57-C-IKKα cells at the three concentrations tested (10–40 µM) (Figure 9A); however, levels of exogenous nuclear IKKα remained unaltered in the presence of apigenin 10–40 µM (Figure 9B), suggesting that the regulation of IKKα by apigenin is post-transcriptional and cannot be exerted when IKKα is localized in the nuclear compartment. To further discard the possible involvement of a transcriptional process in the apigenin-induced inhibition of IKKα, endogenous mouse IKKα mRNA expression was assessed in the three types of C57 cells. The results showed that apigenin did not diminish mouse IKKα expression at 48 h of culture (Figure 9C). Thus, these results suggested that apigenin regulated IKKα expression levels at post-transcriptional level. Next, we analyzed whether apigenin was able to attenuate the molecular changes induced by the exogenous IKKα, which are related to tumor development and progression of cutaneous SCCs. Our results showed that even the lowest concentration of apigenin tested (10 µM) was able to reduce the expression of Akt, Bcl2 and Cyclin D1 and caused the appearance of cleaved-Caspase 3 (CC3) in the three types of C57 cells; furthermore, it was observed that the changes in the expression levels of these proteins were dose-dependent, being more extreme at 40 µM (Figure 9A,B). Since, in prostate cancer cells, the antitumor effect of apigenin was reported to be mediated by its ability to directly interact with IKKα and suppress NF-κB/p65 activation, we analyzed the activation of the NF-κB/p65 subunit (measured as levels of P-p65) in the three types of C57 cells. We found a slight attenuation of NF-κB/p65 activation for 10–40 µM of apigenin tested in the three types of C57 cells (Figure 9A,B), which suggests that in skin carcinoma cells the anti-tumor effect of apigenin is not principally mediated by the inhibition of the NF-κB/p65 pathway. Additionally, we analyzed whether the treatment of C57 cells with apigenin had any effect on the expression levels of Snail1 mRNA. As expected, given the lack of effect of apigenin on nuclear IKKα, we did not find a decrease in the expression levels of Snail1 in C57-N-IKKα cells (Figure 9D), which remained significantly induced in these cells.

3. Discussion

We have analyzed the mechanisms through which IKKα favors mouse cutaneous SCCs aggressiveness. Recent results from our group and others [5,15,16,17] have underscored the relevance of studying the nuclear or cytoplasmic localization of IKKα for the understanding of the mechanisms of the protumoral role of IKKα in NMSC and other types of cancer [15]; therefore, here, we have generated variants of the PDVC57 skin carcinoma cells that express exogenous IKKα in the nucleus or in the cytoplasm. We have found that IKKα confers a greater capacity of migration to the cells in both subcellular localizations, being this effect especially remarkable in the case of the C57-N-IKKα cells. Additionally, C57 cells expressing ectopic IKKα showed increased apoptosis resistance and augmented capacity of survival when they are grown under stress, such as in the absence of serum, i.e., while C57-Control cells showed a strong cleaved-Caspase 3 band (an indicator of apoptosis), there was less amount of cleaved-Caspase 3 in the C57-C-and -N-IKKα cells, which in contrast exhibit greater expression of the prosurvival proteins Bcl2 and Akt. Overexpression of both Bcl2 and Akt has been found in different types of tumors and is associated with EMT, increased invasiveness [48,49,50] and resistance against EGFR-TK inhibitors [51]. The acquisition of migratory properties is a hallmark of cells undergoing EMT changes, which can also be accompanied by a switch toward a mesenchymal phenotype, as occurs in the C57-N-IKKα cells; the increase in the apoptosis resistance and the augmented capacity of survival is another feature of the EMT as well [52]. Therefore, our results suggest that regardless of its subcellular localization, IKKα increases the malignancy of mouse epidermal SCC cells through molecular changes that resemble those of cells undergoing EMT. In addition, we have proven that in another cell line of murine tumor keratinocytes (PB), the C-and-N-IKKα cells share similar alterations to those found in the C57 cells expressing the exogenous IKKα. This finding is in agreement with the role of IKKα in oral SCCs and breast cancer, in which it was reported that IKKα mediated the EMT process induced by TGF-β1, contributing in this way to the tumor-promoting role of this growth factor [53,54]. In addition, in the case of non-small cell lung cancer (NSCLC), our group and others found that IKKα increased the migration of NSCLC cells and promoted NSCLC progression [44,55]. Accordingly, the upregulation of IKKα has been associated with decreased patient survival, and it has been suggested that IKKα levels could overall predict poor clinical outcome in lung adenocarcinoma patients [55]. Thus, given the relevant role that IKKα plays in the progression of different types of human cancer, further studies on the role of C-and-N-IKKα in human tumor keratinocyte cell lines or skin tumors are necessary.
Although our data showed an enhancement of the expression of markers of tumor progression as a consequence of the ectopic expression of IKKα in both localizations, this is even more outstanding in C57-N-IKKα cells, which in addition to the increased levels of MMP9, Akt, Bcl2 and the decreased detection of cleaved-Caspase 3, they induce the expression of c-Myc, that in turn may contribute to the EMT process [43]. Additionally, the overexpression of IKKα in the nucleus of C57 cells causes an acquisition of a marked fibroblastoid phenotype and induces the transcription of Snail1 (which has a pivotal role in the EMT process [56]) and Vimentin, and represses the expression of K5; therefore, the switch in the expression of the epithelial marker K5 toward that of Vimentin correlates with the morphological change detected in the shape of C57-N-IKKα cells [56]; the induction of Snail1 by nuclear IKKα was also observed in NSCLC cells [44]. Altogether, these changes make C57-N-IKKα cells appear as potentially more aggressive, since Snail1 is considered a determinant of the progression of carcinomas [27], c-Myc expression is found in skin SCCs of poor prognosis [57], and the downregulation of the expression of keratins, including that of K5 in skin tumors, is associated with increased malignancy and conversion to spindle cell carcinomas [58].
Therefore, our results here showing that the expression of nuclear IKKα in C57 cells worsen the malignant characteristics of tumor keratinocytes are in agreement with our previous findings in chemical skin carcinogenesis experiments in transgenic mice, which showed that non-tumorigenic keratinocytes expressing increased levels of IKKα in the nucleus lead to an enhanced progression of SCCs [15]; they also agree with results showing that in human patients, skin SCCs expressing higher levels of nuclear IKKα are more aggressive and present higher risk of metastasis [5]. Furthermore, this correlation between nuclear IKKα expression and the worsening of tumor characteristics also applies to lung adenocarcinomas, in which a correlation was found between increased levels of nuclear IKKα and a poor prognosis and lower survival of patients [55,59].
As mentioned, skin SCC is a common type of neoplasia, representing an important problem on patients’ life and clinical management. Although they do not metastasize frequently, once they do, SCCs display considerable aggressiveness, leading to the death of affected individuals and making it necessary to find an effective treatment for this type of cancer. For this reason, we have carried out experiments aimed at further analyzing the mechanisms of action of apigenin, a flavonoid known for its anti-cancer function in diverse types of tumors. In the case of cutaneous SCCs, recently, it has been reported that apigenin inhibits UVB and DMBA/TPA skin carcinogenesis [35,36,60,61]; however, the mechanisms through which it exerts this effect remain largely unknown. In particular, the possible involvement of IKKα in the anti-tumor role of apigenin in NMSC inhibition has not been addressed yet. This is an important issue since, in prostate cancer cells, it was shown that apigenin acted as an anti-cancer agent through its binding to IKKα, which triggered the antitumor response [33].
Here, we have found that apigenin diminishes the expression levels of the ectopic IKKα protein in the cytoplasm but not in the nucleus of C57 cells. This is an interesting result since it was described that the regulation of IKKα by apigenin occurred both in the cytoplasm and in the nucleus of PC3-tumor prostate cells [33]; moreover, in contrast to the results obtained in prostate cancer cells in which one of the main mechanisms of action of apigenin is the IKKα-mediated inhibition of the activation of NF-κB/p65, we have found that, in the C57 cells, apigenin does not inhibit the activation of this signaling pathway in a relevant way, even at high concentrations of apigenin (20–40 µM). On the contrary, we have found that apigenin attenuates the expression of proteins recognized as key molecules for skin cancer progression, such as Cyclin D1, Akt and Bcl2, while inducing the cleaving of Caspase 3, which plays a central role in apoptosis. Additionally, our results also show that apigenin downregulates IKKα at post-transcriptional level, since we did not find differences in the expression of the endogenous mouse IKKα mRNA (the expression of the ectopic IKKα is under the control of the β-actin promoter; thus, it is not subjected to the regulatory elements of the endogenous IKKα gene). Our results also complement those reported by other groups which described that apigenin exerted, at least in part, its anticancer effect in the nucleus of cells. It was reported that apigenin interacted with DNA in prostate cancer cells [62] and that it was involved in mRNA metabolism/splicing in the nucleus of breast cancer cells [63]. Therefore, further research work is needed to investigate whether the mechanism of action of apigenin is cell-type specific, since in our models of PDVC57 cells apigenin does not affect nuclear IKKα, while it is able to diminish levels of cytoplasmic IKKα. It would be interesting to study the mechanism/s through which this reduction takes place, i.e., whether there is a direct interaction apigenin-IKKα or if the formation of a complex with another molecule is required.
Therefore, our findings are noteworthy as they suggest that apigenin could be a promising anti-NMSC drug therapy since, in addition to reducing the levels of IKKα, which favors skin SCC progression, it reduces those of Cyclin D1, Akt and Bcl2, which also play a relevant role in NMSC malignization. However, it has been described that cutaneous SCC with higher risk to metastasize express higher levels of nuclear IKKα [5]; thus, it would be interesting to study whether these aggressive tumors, in addition to elevated levels of nuclear IKKα, also express high levels of cytoplasmic IKKα, and whether the changes in the expression levels of the aforementioned proteins -Cyclin D1, Bcl2, Akt- by apigenin are dependent or not in the reduction of the cytoplasmic IKKα levels.
In summary, our model of C57 skin carcinoma cells that express ectopic IKKα in the nucleus is a valuable model to study the molecular mechanisms that lead to the enhanced aggressiveness of cutaneous SCCs with high risk to metastasize (that contains elevated levels of nuclear IKKα). In addition, our data suggest that IKKα may be a therapeutic target for the treatment of skin SCCs and that apigenin could be a potential anti-NMSC cancer treatment. Moreover, and given the relevance of the subcellular localization of IKKα for the development of NMSC, our model of C57-C-and-N-IKKα cells provides a powerful tool to analyze whether IKKα inhibitors are capable of targeting IKKα when localized to a specific subcellular compartment.

4. Materials and Methods

4.1. DNA Constructs

The C-and-N-IKKα constructs have been previously described [15]. Briefly, both of them contain the sequence of the human IKKα gene cDNA, but the N-IKKα construct has an extra NLS (nuclear localization signal) in 5′; in contrast, in the C-IKKα construct, the internal NLS site was removed. Both constructs were subcloned in the pRC vector containing the β-Actin promoter (25) and the Flag-tag. The empty pRC-βActin vector was used as a Control (C57-Control cells). All constructs confer resistance to G418.

4.2. Cells, Culture Conditions and Transfection Assays

PDVC57 and PB cells were provided by Dr. Miguel Quintanilla (Instituto de Investigaciones Biomédicas (IIBM), Madrid, Spain. They were cultured in DMEM-10% FBS. They were permanently transfected using the calcium phosphate method and selected using G418 (0.45 mg/mL, BioNova, Fremont, CA, USA).

4.3. Colony Forming Assays

A total of 5 × 102 and 1 × 103 cells were seeded per duplicate in DMEM-10% FBS in p100 plates. Medium was replaced every 2 days. Growing colonies were photographed at different time points. Experiments were performed three times per duplicate.

4.4. Wound Healing Assays

Cells growing in monolayer cultures were incubated 2 h at 37 °C in DMEM plus 5 mg/mL of mitomycin C; then washed with PBS. After 1 h, a scratch wound was created in vitro by scraping the cell monolayer with a sterile pipette tip. Healing was measured at 48 h post-scratch. Three experiments were performed by duplicate.

4.5. Growth in Serum-Free Medium

Next, 2 × 106 cells were seeded into p100-plates in complete medium. After 24 h, the medium was replaced by serum-free DMEM. Cells were collected 7 days later. Three experiments were performed by duplicate.

4.6. Cell Viability Assay

The effect of apigenin on the viability of C57 cells of the three genotypes was evaluated. Next, 5 × 104 cells were seeded onto p60 plates in complete medium (DMEM-10% FBS). Following incubation overnight, the cells were treated with 10 or 20 µM apigenin in dimethyl sulfoxide (DMSO) for 24, 48 and 72 h in a humidified atmosphere of 5% CO2 at 37 °C. Following incubation for the indicated times, cells were trypsinized and counted with a Neubauer’s chamber. Three experiments per duplicate were performed. The results were expressed as a percentage of growth.

4.7. Immunofluorescence Staining

Cells grown in coverslips were fixed in methanol/acetone (1/1). Primary antibodies used were: anti-Flag antibody (F3040, Sigma-Aldrich, St. Louis, MO, USA); anti-K5 (PRB-160P) (Biolegend, San Diego, CA, USA); and anti-IKKα (NB100-56704, Novus Biologicals, Cambridge, UK).

4.8. Western Blot Analysis

Total protein extracts (40 μg) were subjected to SDS/PAGE. The separated proteins were transferred to nitrocellulose membranes (Amersham, Arlington Heights, IL, USA; BioRad, Marnes-la-Coquette, France) and probed with antibodies against IKKα (NB100-56704) (Novus Biologicals, Cambridge, UK); c-Myc (626802; Biolegend, San Diego, CA, USA); Actin (6276; Abcam, Cambridge, UK); GAPDH (sc-32233; Santa Cruz Biotechnology Inc. Europe, Heidelberg, Germany); MMP9 (AB19016; Merck Millipore, Darmstadt, Germany); Bcl2 (3498), cleaved-Caspase 3 (9661), Akt (4691) and P-p65 (3039) (Cell Signaling Technology, Danvers, MA, USA); Cyclin D1 (MA5-16356; Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). In all cases, samples were subjected to luminography with the Supersignal West Pico Chemiluminescent Substrate (Pierce Biotechnology Inc., Rockford, IL, USA) or with Clarity Western ECL Substrate, 1705061 (BioRad, Marnes-la-Coquette, France).

4.9. RNA Isolation and Quantitative RT-qPCR Analysis

Total RNA from C57 cells of the three genotypes was isolated using miRNeasy Mini Kit (Qiagen), and DNA was eliminated with an Rnase-Free DNase Set (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. The reverse transcription reaction was performed using the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Waltham, MA, USA) for mRNA. Quantitative qRT-PCR was performed in a 7500 Fast Real Time PCR System using GoTaq qPCR Master Mix (Promega, Maddison, WI, USA) for mRNA. The sequences of the oligonucleotides specific for Snail1 and mouse IKKα used are listed in Table 1. TBP was used as a housekeeping for normalization of gene expression. Fold changes were calculated using the efficiency-corrected model [64], given by the formula Ratio = (ETARGET)∆CtTARGET/(EREF)∆CtREF, being E the amplification efficiency of the target or the reference genes, Ct the cycle threshold and ΔCtTARGET is the Ct difference of a treated and control sample for the target gene (i.e., ΔCtTARGET = CtCONTROL−CtTREATED), and ΔCtREF is the Ct difference of a treated and control sample for the reference gene (i.e., ΔCtREF = CtCONTROL−CtTREATED).

Supplementary Materials

The following supporting information can be downloaded at: www.mdpi.com/article/10.3390/ijms23031375/s1.

Author Contributions

Conception and design of experiments, V.A.G.-G., J.P.A. and M.L.C.; Data acquisition, V.A.G.-G., J.P.A., A.P., A.M.-G., A.T., R.A.G.-F. and M.L.C.; Data analysis and interpretation, V.A.G.-G., J.P.A., A.P., J.M.P., M.N. and M.L.C.; Writing—original draft preparation, M.L.C.; Writing—review and editing, M.L.C., V.A.G.-G., J.P.A., A.P., M.N. and J.M.P.; Supervision, M.L.C.; Funding acquisition, M.N., J.M.P. and M.L.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the following projects from the “Instituto de Salud Carlos III” (Ministry of Science, Innovation and Universities) and co-funded by the European Regional Development Fund (FEDER): PI19/01262 to M.L.C.; PI20/01173 to M.N.; CIBERONC no. CB16/12/00228 and PID2019-110758RB-I00 to J.M.P. It was also funded by the Instituto de Investigación Hospital 12 de Octubre (i + 12), project “i12-AY201228-1” to M.L.C. Adrián Tejero is employed by the Comunidad Autónoma de Madrid (CAM) and by the European Social Fund within the Operational Program for Youth Employment, for the programming period 2021–2022, as well as the Youth Employment Initiative (YEI).

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank Federico Sánchez-Sierra and Pilar Hernández for their excellent histological processing of the samples.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Abbreviations

BCCsbasal cell carcinomas
CC3cleaved-Caspase 3
EMTepithelial–mesenchymal transition
FBSfetal bovine serum
NMSCnon melanoma skin cancer
NSCLCnon-small cell lung cancer
RDEBrecessive epidermolysis bullosa
SCCssquamous cell carcinomas

References

  1. Christenson, L.J.; Borrowman, T.A.; Vachon, C.M.; Tollefson, M.M.; Otley, C.C.; Weaver, A.L.; Roenigk, R.K. Incidence of basal cell and squamous cell carcinomas in a population younger than 40 years. JAMA 2005, 294, 681–690. [Google Scholar] [CrossRef] [Green Version]
  2. Karia, P.S.; Han, J.; Schmults, C.D. Cutaneous squamous cell carcinoma: Estimated incidence of disease, nodal metastasis, and deaths from disease in the United States, 2012. J. Am. Acad. Dermatol. 2013, 68, 957–966. [Google Scholar] [CrossRef]
  3. Condorelli, A.G.; Dellambra, E.; Logli, E.; Zambruno, G.; Castiglia, D. Epidermolysis Bullosa-associated squamous cell carcinoma: From pathogenesis to therapeutic perspectives. Int. J. Mol. Sci. 2019, 20, 5707. [Google Scholar] [CrossRef] [Green Version]
  4. Mittal, A.; Colegio, O.R. Skin cancers in organ transplant recipients. Am. J. Transplant. 2017, 17, 2509–2530. [Google Scholar] [CrossRef]
  5. Toll, A.; Margalef, P.; Masferrer, E.; Ferrándiz-Pulido, C.; Gimeno, J.; Pujol, R.M.; Bigas, A.; Espinosa, L. Active nuclear IKK correlates with metastatic risk in cutaneous squamous cell carcinoma. Arch. Dermatol. Res. 2015, 21, 21. [Google Scholar] [CrossRef]
  6. Hayden, M.S.; Ghosh, S. Signaling to NF-kappaB. Genes Dev. 2004, 18, 2195–2224. [Google Scholar] [CrossRef] [Green Version]
  7. Li, Q.; Lu, Q.; Hwang, J.W.; Büscher, D.; Lee, K.F.; Izpisua-Belmonte, J.C.; Verma, I.M. IKK1-deficient mice exhibit abnormal development of skin and skeleton. Genes Dev. 1999, 13, 1322–1328. [Google Scholar] [CrossRef]
  8. Takeda, K.; Takeuchi, O.; Tsujimura, T.; Itami, S.; Adachi, O.; Kawai, T.; Sanjo, H.; Yoshikawa, K.; Terada, N.; Akira, S. Limb and skin abnormalities in mice lacking IKKalpha. Science 1999, 284, 313–316. [Google Scholar] [CrossRef]
  9. Anest, V.; Hanson, J.L.; Cogswell, P.C.; Steinbrecher, K.A.; Strahl, B.D.; Baldwin, A.S. A nucleosomal function for IkappaB kinase-alpha in NF-kappaB-dependent gene expression. Nature 2003, 423, 659–663. [Google Scholar] [CrossRef] [Green Version]
  10. Luo, J.L.; Tan, W.; Ricono, J.M.; Korchynskyi, O.; Zhang, M.; Gonias, S.L.; Cheresh, D.A.; Karin, M. Nuclear cytokine-activated IKKalpha controls prostate cancer metastasis by repressing Maspin. Nature 2007, 446, 690–694. [Google Scholar] [CrossRef]
  11. Fernandez-Majada, V.; Aguilera, C.; Villanueva, A.; Vilardell, F.; Robert-Moreno, A.; Aytés, A.; Real, F.X.; Capella, G.; Mayo, M.W.; Espinosa, L.; et al. Nuclear IKK activity leads to dysregulated notch-dependent gene expression in colorectal cancer. Proc. Natl. Acad. Sci. USA 2007, 104, 276–281. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Hu, Y.; Baud, V.; Delhase, M.; Zhang, P.; Deerinck, T.; Ellisman, M.; Johnson, R.; Karin, M. Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase. Science 1999, 284, 316–320. [Google Scholar] [CrossRef] [PubMed]
  13. Li, Q.; Van Antwerp, D.; Mercurio, F.; Lee, K.F.; Verma, I.M. Severe liver degeneration in mice lacking the IkappaB kinase 2 gene. Science 1999, 284, 321–325. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Sil, A.K.; Maeda, S.; Sano, Y.; Roop, D.R.; Karin, M. IkappaB kinase-alpha acts in the epidermis to control skeletal and craniofacial morphogenesis. Nature 2004, 428, 660–664. [Google Scholar] [CrossRef]
  15. Alameda, J.P.; Gaspar, M.; Ramírez, A.; Navarro, M.; Page, A.; Suárez-Cabrera, C.; Fernández, M.G.; Mérida, J.R.; Paramio, J.M.; García-Fernández, R.-A.; et al. Deciphering the role of nuclear and cytoplasmic IKKalpha in skin cancer. Oncotarget 2016, 7, 29531–29547. [Google Scholar] [CrossRef]
  16. Alameda, J.P.; Moreno-Maldonado, R.; Fernández-Aceñero, M.J.; Navarro, N.; Page, A.; Jorcano, J.L.; Bravo, A.; Ramírez, A.; Casanova, M.L. Increased IKKalpha expression in the Basal layer of the epidermis of transgenic mice enhances the malignant potential of skin tumors. PLoS ONE 2011, 6, e21984. [Google Scholar] [CrossRef]
  17. Moreno-Maldonado, R.; Ramírez, A.; Navarro, M.; Fernández-Aceñero, M.J.; Villanueva, C.; Page, A.; Jorcano, J.L.; Bravo, A.; Casanova, M.L. IKKalpha enhances human keratinocyte differentiation and determines the histological variant of epidermal squamous cell carcinomas. Cell Cycle 2008, 7, 2021–2029. [Google Scholar] [CrossRef] [Green Version]
  18. Liu, B.; Park, E.; Zhu, F.; Bustos, T.; Liu, J.; Shen, J.; Fischer, S.M.; Hu, Y. A critical role for I kappaB kinase alpha in the development of human and mouse squamous cell carcinomas. Proc. Natl. Acad. Sci. USA 2006, 103, 17202–17207. [Google Scholar] [CrossRef] [Green Version]
  19. Saitoh, M. Involvement of partial EMT in cancer progression. J. Biochem. 2018, 164, 257–264. [Google Scholar] [CrossRef] [Green Version]
  20. Thiery, J.P.; Acloque, H.; Huang, R.Y.J.; Nieto, M.A. Epithelial-mesenchymal transitions in development and disease. Cell 2009, 139, 871–890. [Google Scholar] [CrossRef]
  21. Dongre, A.; Weinberg, R.A. New insights into the mechanisms of epithelial-mesenchymal transition and implications for cancer. Nat. Rev. Mol. Cell Biol. 2019, 20, 69–84. [Google Scholar] [CrossRef] [PubMed]
  22. Leggett, S.E.; Hruska, A.M.; Guo, M.; Wong, Y. The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems. Cell Commun. Signal. 2021, 19, 32. [Google Scholar] [CrossRef] [PubMed]
  23. Scheau, C.; Badarau, I.A.; Costache, R.; Caruntu, C.; Mihai, G.L.; Didilescu, A.C.; Constantin, C.; Neagu, M. The role of matrix metalloproteinases in the epithelial-mesenchymal transition of hepatocellular carcinoma. Anal. Cell Pathol. 2019, 2019, 9423907. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Tiwari, N.; Gheldof, A.; Tatari, M.; Christofori, G. EMT as the ultimate survival mechanism of cancer cells. Semin. Cancer Biol. 2012, 22, 194–207. [Google Scholar] [CrossRef] [PubMed]
  25. Robson, E.J.; Khaled, W.T.; Abell, K.; Watson, C.J. Epithelial-to-mesenchymal transition confers resistance to apoptosis in three murine mammary epithelial cell lines. Differentiation 2006, 74, 254–264. [Google Scholar] [CrossRef]
  26. Kurrey, N.K.; Jalgaonkar, S.P.; Joglekar, A.V.; Ghanate, A.D.; Chaskar, P.D.; Doiphode, R.Y.; Bapat, S.A. Snail and slug mediate radioresistance and chemoresistance by antagonizing p53-mediated apoptosis and acquiring a stem-like phenotype in ovarian cancer cells. Stem Cells 2009, 27, 2059–2068. [Google Scholar] [CrossRef]
  27. Nieto, M.A. The snail superfamily of zinc-finger transcription factors. Nat. Rev. Mol. Cell Biol. 2002, 3, 155–166. [Google Scholar] [CrossRef]
  28. Smith, B.N.; Bhowmick, N.A. Role of EMT in metastasis and therapy resistance. J. Clin. Med. 2016, 5, 17. [Google Scholar] [CrossRef] [Green Version]
  29. Ashrafizadeh, M.; Zarrabi, A.; Hushmandi, K.; Kalantari, M.; Mohammadinejad, R.; Javaheri, T.; Sethi, G. Association of the Epithelial-Mesenchymal Transition (EMT) with cisplatin resistance. Int. J. Mol. Sci. 2020, 21, 4002. [Google Scholar] [CrossRef]
  30. Saenz-Sardà, X.; Carrato, C.; Pérez-Roca, L.; Puig, L.; Ferrándiz, C.; Ariza, A.; Fernández-Figueras, M.T. Epithelial-to-mesenchymal transition contributes to invasion in squamous cell carcinomas originated from actinic keratosis through the differentiated pathway, whereas proliferation plays a more significant role in the classical pathway. J. Eur. Acad. Dermatol. Venereol. 2018, 32, 581–586. [Google Scholar] [CrossRef]
  31. Barrette, K.; Van Kelst, S.; Wouters, J.; Marasigan, V.; Fieuws, S.; Agostinis, P.; van den Oord, J.; Garmyn, M. Epithelial-mesenchymal transition during invasion of cutaneous squamous cell carcinoma is paralleled by AKT activation. Br. J. Dermatol. 2014, 171, 1014–1021. [Google Scholar] [CrossRef] [PubMed]
  32. Ashrafizadeh, M.; Bakhoda, M.R.; Bahmanpour, Z.; Ilkhani, K.; Zarrabi, A.; Makvandi, P.; Khan, H.; Mazaheri, S.; Darvish, M.; Mirzaei, H. Apigenin as tumor suppressor in cancers: Biotherapeutic activity, nanodelivery, and mechanisms with emphasis on pancreatic cancer. Front. Chem. 2020, 8, 829. [Google Scholar] [CrossRef] [PubMed]
  33. Shukla, S.; Kanwal, R.; Shankar, E.; Datt, M.; Chance, M.R.; Fu, P.; MacLennan, G.T.; Gupta, S. Apigenin blocks IKKalpha activation and suppresses prostate cancer progression. Oncotarget 2015, 6, 31216–31232. [Google Scholar] [CrossRef] [PubMed]
  34. Shukla, S.; Shankar, E.; Fu, P.; MacLennan, G.T.; Gupta, S. Suppression of NF-κB and NF-κB-regulated gene expression by apigenin through IκBα and IKK pathway in TRAMP mice. PLoS ONE 2015, 10, e0138710. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Kiraly, A.J.; Soliman, E.; Jenkins, A.; Van Dross, R.T. Apigenin inhibits COX-2, PGE2, and EP1 and also initiates terminal differentiation in the epidermis of tumor bearing mice. Prostaglandins Leukot. Essent. Fatty Acids 2016, 104, 44–53. [Google Scholar] [CrossRef] [PubMed]
  36. Mirzoeva, S.; Tong, X.; Bridgeman, B.B.; Plebanek, M.P.; Volpert, O.V. Apigenin inhibits UVB-induced skin carcinogenesis: The role of thrombospondin-1 as an anti-inflammatory factor. Neoplasia 2018, 20, 930–942. [Google Scholar] [CrossRef]
  37. Pierceall, W.E.; Goldberg, L.H.; Tainsky, M.A.; Mukhopadhyay, T.; Ananthaswamy, H.N. Ras gene mutation and amplification in human nonmelanoma skin cancers. Mol. Carcinog. 1991, 4, 196–202. [Google Scholar] [CrossRef]
  38. Spencer, J.M.; Kahn, S.M.; Jiang, W.; DeLeo, V.A.; Weinstein, I.B. Activated ras genes occur in human actinic keratoses, premalignant precursors to squamous cell carcinomas. Arch. Dermatol. 1995, 131, 796–800. [Google Scholar] [CrossRef]
  39. Caulin, C.; Bauluz, C.; Gandarillas, A.; Cano, A.; Quintanilla, M. Changes in keratin expression during malignant progression of transformed mouse epidermal keratinocytes. Exp. Cell Res. 1993, 204, 11–21. [Google Scholar] [CrossRef]
  40. Larcher, F.; Robles, A.I.; Duran, H.; Murillas, R.; Quintanilla, M.; Cano, A.; Conti, C.J.; Jorcano, J.L. Up-regulation of vascular endothelial growth factor/vascular permeability factor in mouse skin carcinogenesis correlates with malignant progression state and activated H-ras expression levels. Cancer Res. 1996, 56, 5391–5396. [Google Scholar]
  41. Eriksson, J.E.; Dechat, T.; Grin, B.; Helfand, B.; Mendez, M.; Pallari, H.M.; Goldman, R.D. Introducing intermediate filaments: From discovery to disease. J. Clin. Investig. 2009, 119, 1763–1771. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Shchors, K.; Nozawa, H.; Xu, J.; Rostker, F.; Swigart-Brown, L.; Evan, G.; Hanahan, D. Increased invasiveness of MMP-9-deficient tumors in two mouse models of neuroendocrine tumorigenesis. Oncogene 2013, 32, 502–513. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Cho, K.B.; Cho, M.K.; Lee, W.Y.; Kang, K.W. Overexpression of c-myc induces epithelial mesenchymal transition in mammary epithelial cells. Cancer Lett. 2010, 293, 230–239. [Google Scholar] [CrossRef] [PubMed]
  44. Page, A.; Ortega, A.; Alameda, J.P.; Navarro, M.; Paramio, J.M.; Saiz-Pardo, M.; Almeida, E.I.; Hernández, P.; Fernández-Aceñero, M.-J.; García-Fernández, R.A.; et al. IKKα promotes the progression and metastasis of non-small cell lung cancer independently of its subcellular localization. Comput. Struct. Biotechnol. J. 2019, 17, 251–262. [Google Scholar] [CrossRef]
  45. Yuspa, S.H.; Morgan, D.; Lichti, U.; Spangler, E.F.; Michael, D.; Kilkenny, A.; Hennings, H. Cultivation and characterization of cells derived from mouse skin papillomas induced by an initiation-promotion protocol. Carcinogenesis 1986, 7, 949–958. [Google Scholar] [CrossRef]
  46. Vivanco, I.; Chen, Z.C.; Tanos, B.; Oldrini, B.; Hsieh, W.Y.; Yannuzzi, N.; Campos, C.; Mellinghoff, I.K. A kinase-independent function of AKT promotes cancer cell survival. Elife 2014, 3, e03751. [Google Scholar] [CrossRef]
  47. Shukla, S.; Bhaskaran, N.; Babcook, M.A.; Fu, P.; Maclennan, G.T.; Gupta, S. Apigenin inhibits prostate cancer progression in TRAMP mice via targeting PI3K/Akt/FoxO pathway. Carcinogenesis 2014, 35, 452–460. [Google Scholar] [CrossRef] [Green Version]
  48. Altomare, D.A.; Testa, J.R. Perturbations of the AKT signaling pathway in human cancer. Oncogene 2005, 24, 7455–7464. [Google Scholar] [CrossRef] [Green Version]
  49. Du, C.; Zhang, X.; Yao, M.; Lv, K.; Wang, J.; Chen, L.; Chen, Y.; Wang, S.; Fu, P. Bcl-2 promotes metastasis through the epithelial-to-mesenchymal transition in the BCap37 medullary breast cancer cell line. Oncol Lett. 2018, 15, 8991–8998. [Google Scholar] [CrossRef] [Green Version]
  50. Grille, S.J.; Bellacosa, A.; Upson, J.; Klein-Szanto, A.J.; van Roy, F.; Lee-Kwon, W.; Donowitz, M.; Tsichlis, F.N.; Larue, L. The protein kinase Akt induces epithelial mesenchymal transition and promotes enhanced motility and invasiveness of squamous cell carcinoma lines. Cancer Res. 2003, 63, 2172–2178. [Google Scholar]
  51. Cheong, H.T.; Xu, F.; Choy, C.T.; Hui, C.W.C.; Mok, T.S.K.; Wong, C.W. Upregulation of Bcl2 in NSCLC with acquired resistance to EGFR-TKI. Oncol Lett. 2018, 15, 901–907. [Google Scholar] [CrossRef] [PubMed]
  52. Kalluri, R.; Weinberg, R.A. The basics of epithelial-mesenchymal transition. J. Clin. Investig. 2009, 119, 1420–1428. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Lv, S.; Luo, T.; Yang, Y.; Li, Y.; Yang, J.; Xu, J.; Zheng, J.; Zeng, Y. Naa10p and IKKα interaction regulates EMT in oral squamous cell carcinoma via TGF-β1/Smad pathway. J. Cell. Mol. Med. 2021, 25, 6760–6772. [Google Scholar] [CrossRef] [PubMed]
  54. Brandl, M.; Seidler, B.; Haller, F.; Adamski, J.; Schmid, R.M.; Saur, D.; Schneider, G. IKK(α) controls canonical TGF(ß)-SMAD signaling to regulate genes expressing SNAIL and SLUG during EMT in panc1 cells. J. Cell Sci. 2010, 123 Pt 24, 4231–4239. [Google Scholar] [CrossRef] [Green Version]
  55. Alam, S.K.; Astone, M.; Liu, P.; Hall, S.R.; Coyle, A.M.; Dankert, E.N.; Hoffman, D.K.; Zhang, W.; Kuang, R.; Roden, A.C.; et al. DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKalpha-dependent cell migration. Commun. Biol. 2018, 1, 43. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Kaufhold, S.; Bonavida, B. Central role of Snail1 in the regulation of EMT and resistance in cancer: A target for therapeutic intervention. J. Exp. Clin. Cancer Res. 2014, 33, 62. [Google Scholar] [CrossRef] [PubMed]
  57. Toll, A.; Salgado, R.; Yébenes, M.; Martín-Ezquerra, G.; Gilaberte, M.; Baró, T.; Solé, F.; Alameda, F.; Espinet, B.; Pujol, R.M. MYC gene numerical aberrations in actinic keratosis and cutaneous squamous cell carcinoma. Br. J. Dermatol. 2009, 161, 1112–1118. [Google Scholar] [CrossRef]
  58. Stoler, A.B.; Stenback, F.; Balmain, A. The conversion of mouse skin squamous cell carcinomas to spindle cell carcinomas is a recessive event. J. Cell Biol. 1993, 122, 1103–1117. [Google Scholar] [CrossRef]
  59. Vreka, M.; Lilis, I.; Papageorgopoulou, M.; Giotopoulou, G.A.; Lianou, M.; Giopanou, I.; Kanellakis, N.I.; Spella, M.; Agalioti, T.; Armenis, V.; et al. IkappaB Kinase alpha is required for development and progression of KRAS-mutant lung adenocarcinoma. Cancer Res. 2018, 78, 2939–2951. [Google Scholar] [CrossRef] [Green Version]
  60. Wei, H.; Tye, L.; Bresnick, E.; Birt, D.F. Inhibitory effect of apigenin, a plant flavonoid, on epidermal ornithine decarboxylase and skin tumor promotion in mice. Cancer Res. 1990, 50, 499–502. [Google Scholar]
  61. Birt, D.F.; Mitchell, D.; Gold, B.; Pour, P.; Pinchet, H.C. Inhibition of ultraviolet light induced skin carcinogenesis in SKH-1 mice by apigenin, a plant flavonoid. Anticancer Res. 1997, 17, 85–91. [Google Scholar]
  62. Sharma, H.; Kanwal, R.; Bhaskaran, N.; Gupta, S. Plant flavone apigenin binds to nucleic acid bases and reduces oxidative DNA damage in prostate epithelial cells. PLoS ONE 2014, 9, e91588. [Google Scholar] [CrossRef] [Green Version]
  63. Arango, D.; Morohashi, K.; Yilmaz, A.; Kuramochi, K.; Parihar, A.; Brahimaj, B.; Grotewold, E.; Doseff, A.I. Molecular basis for the action of a dietary flavonoid revealed by the comprehensive identification of apigenin human targets. Proc. Natl. Acad. Sci. USA 2013, 110, E2153–E2162. [Google Scholar] [CrossRef] [Green Version]
  64. Khan-Malek, R.; Wang, Y. Statistical analysis of quantitative RT-PCR results. Methods Mol. Biol. 2017, 1641, 281–296. [Google Scholar]
Ijms 23 01375 g001 550
Figure 1. Generation of the C57-C-and N-IKKα clones. (A) Western blots showing the expression of the exogenous IKKα in the C57-C–and-N-IKKα cells (upper arrow). The expression in different selected clones is shown. Actin was used as loading control. hIKKα: exogenous human IKKα protein; mIKKα: endogenous mouse IKKα protein. (B–H) Immunofluorescence analysis of the expression of the transgenic protein in the C57-Control, C57-C-IKKα and C57-N-IKKα cells. An anti-Flag antibody was used. (B) In the C57-Control cells, transfected with the empty vector, Flag is not detected. (C,E) Cytoplasmic expression of the Flag reporter in the C57-C-IKKα cells transfected with the β-actin-C-IKKα construct. (F,H) Nuclear expression of Flag is observed in C57-N-IKKα cells transfected with the β-actin-N-IKKα construct. (D,G) Dapi stainings mark the nuclei. Scale bar: 40 μm.
Figure 1. Generation of the C57-C-and N-IKKα clones. (A) Western blots showing the expression of the exogenous IKKα in the C57-C–and-N-IKKα cells (upper arrow). The expression in different selected clones is shown. Actin was used as loading control. hIKKα: exogenous human IKKα protein; mIKKα: endogenous mouse IKKα protein. (B–H) Immunofluorescence analysis of the expression of the transgenic protein in the C57-Control, C57-C-IKKα and C57-N-IKKα cells. An anti-Flag antibody was used. (B) In the C57-Control cells, transfected with the empty vector, Flag is not detected. (C,E) Cytoplasmic expression of the Flag reporter in the C57-C-IKKα cells transfected with the β-actin-C-IKKα construct. (F,H) Nuclear expression of Flag is observed in C57-N-IKKα cells transfected with the β-actin-N-IKKα construct. (D,G) Dapi stainings mark the nuclei. Scale bar: 40 μm.
Ijms 23 01375 g001
Ijms 23 01375 g002 550
Figure 2. Appearance of C57 cells of each genotype growing in culture. (A–F) Representative images of two different clones of C57 cells of the three genotypes growing for 72 h. Note the contrast between the epithelial morphology of C57-Control (A,B) and C57-C-IKKα (C,D) cells and the fibroblastoid morphology of C57-N-IKKα cells (E,F). Co1, Co2: C57-Control 1 and C57-Control 2 clones, respectively; C4, C8: C57-C-IKKα clones C4 and C8, respectively; N3, N4: C57-N-IKKα clones N3 and N4, respectively. Scale bars: 50 μm.
Figure 2. Appearance of C57 cells of each genotype growing in culture. (A–F) Representative images of two different clones of C57 cells of the three genotypes growing for 72 h. Note the contrast between the epithelial morphology of C57-Control (A,B) and C57-C-IKKα (C,D) cells and the fibroblastoid morphology of C57-N-IKKα cells (E,F). Co1, Co2: C57-Control 1 and C57-Control 2 clones, respectively; C4, C8: C57-C-IKKα clones C4 and C8, respectively; N3, N4: C57-N-IKKα clones N3 and N4, respectively. Scale bars: 50 μm.
Ijms 23 01375 g002
Ijms 23 01375 g003 550
Figure 3. Morphological changes of the colonies formed by C57 cells expressing the ectopic IKKα. Representative images showing the appearance of the colonies formed by C57 cells of the three genotypes four (A–H) and eleven (I–K) days after seeding. Observe that C57-Control cells form rounded and compact colonies with a well-defined border (A,B). By contrast, colonies formed by C57-N-IKKα cells appear loose, with cells disposed in parallel (bracket) and show the presence of migratory cells moving away from the core of the colony (red arrows) (D,E). Colonies formed by C57-C-IKKα cells show an intermediate phenotype between that of C57-Control and C57-N-IKKα cells: occasional migratory cells in the periphery of the colonies are detected (red arrows) (F–H). (I–K) At eleven days post seeding, foci of migratory cells were detected (red arrows) in C57-N-IKKα (J) and C57-C-IKKα (K) cells. Bracket in (J) points to foci of loose cells. Co1, Co2: C57-Control 1 and C57-Control 2 clones, respectively; C4, C8: C57-C-IKKα clones C4 and C8, respectively; N3, N4: C57-N-IKKα clones N3 and N4, respectively. Scale bars: (A–H) 50 μm; (I–K) 150 μm.
Figure 3. Morphological changes of the colonies formed by C57 cells expressing the ectopic IKKα. Representative images showing the appearance of the colonies formed by C57 cells of the three genotypes four (A–H) and eleven (I–K) days after seeding. Observe that C57-Control cells form rounded and compact colonies with a well-defined border (A,B). By contrast, colonies formed by C57-N-IKKα cells appear loose, with cells disposed in parallel (bracket) and show the presence of migratory cells moving away from the core of the colony (red arrows) (D,E). Colonies formed by C57-C-IKKα cells show an intermediate phenotype between that of C57-Control and C57-N-IKKα cells: occasional migratory cells in the periphery of the colonies are detected (red arrows) (F–H). (I–K) At eleven days post seeding, foci of migratory cells were detected (red arrows) in C57-N-IKKα (J) and C57-C-IKKα (K) cells. Bracket in (J) points to foci of loose cells. Co1, Co2: C57-Control 1 and C57-Control 2 clones, respectively; C4, C8: C57-C-IKKα clones C4 and C8, respectively; N3, N4: C57-N-IKKα clones N3 and N4, respectively. Scale bars: (A–H) 50 μm; (I–K) 150 μm.
Ijms 23 01375 g003
Ijms 23 01375 g004 550
Figure 4. Wound healing assay. Cell pictures at the time of the scratch (0 h) of the two selected clones of each genotype are presented (A,C,E,G,I,K); below, migration 48 h after the scratch wound is shown (B,D,F,H,J,L). Note the increased number of foci of migrating cells of both the C57-N- and-C-IKKα cells (red arrows) (F,H,J,L); also the migration distance is longer in C57 cells expressing the exogenous IKKα (double head red arrows); discontinued red lines indicate the position in which the migration initiates in each cell type. In C57-Control cells, few migratory cells are detected (B,D). (M) Graphic representation of the number of foci of migration found per 6 cm wound length. Data are shown as mean ± SEM; * p < 0.05 by t test. Scale bars: (A,C,E,G,I,K) 100 μm; (B,D,F,H,J,L) 70 μm.
Figure 4. Wound healing assay. Cell pictures at the time of the scratch (0 h) of the two selected clones of each genotype are presented (A,C,E,G,I,K); below, migration 48 h after the scratch wound is shown (B,D,F,H,J,L). Note the increased number of foci of migrating cells of both the C57-N- and-C-IKKα cells (red arrows) (F,H,J,L); also the migration distance is longer in C57 cells expressing the exogenous IKKα (double head red arrows); discontinued red lines indicate the position in which the migration initiates in each cell type. In C57-Control cells, few migratory cells are detected (B,D). (M) Graphic representation of the number of foci of migration found per 6 cm wound length. Data are shown as mean ± SEM; * p < 0.05 by t test. Scale bars: (A,C,E,G,I,K) 100 μm; (B,D,F,H,J,L) 70 μm.
Ijms 23 01375 g004
Ijms 23 01375 g005 550
Figure 5. Induction in the C57-N-IKKα cells of the expression of the EMT master gene Snail1 and repression of the K5 epithelial marker. (A) The analysis by qPCR of the expression of Snail1 shows that it is induced in the C57-N-IKKα cells (arbitrary units). (B) qPCR analysis showing the increased expression of Vimentin in the C57-N-IKKα cells (arbitrary units). Data are shown as mean ± SEM; * p < 0.05 by two-tailed unpaired t test with Welch’s correction. (C–E) Immunofluorescence staining with anti-IKKα (green) and anti-K5 (red) antibodies. (C) C57-Control cells show co-expression of both IKKα and K5 in each cell. (D) Observe that in the C57-N- IKKα cells, most cells express IKKα in the nucleus (green) and do not express K5 (asterisks), and on the contrary, those scarce cells that do not express nuclear IKKα express K5 (arrows). (E) Both, IKKα and K5, are co-expressed in almost all C57-C-IKKα cells, although sporadically it can be observed the presence of cells that express IKKα in the cytoplasm but do not express K5 (asterisks). Scale bars: 35 μm.
Figure 5. Induction in the C57-N-IKKα cells of the expression of the EMT master gene Snail1 and repression of the K5 epithelial marker. (A) The analysis by qPCR of the expression of Snail1 shows that it is induced in the C57-N-IKKα cells (arbitrary units). (B) qPCR analysis showing the increased expression of Vimentin in the C57-N-IKKα cells (arbitrary units). Data are shown as mean ± SEM; * p < 0.05 by two-tailed unpaired t test with Welch’s correction. (C–E) Immunofluorescence staining with anti-IKKα (green) and anti-K5 (red) antibodies. (C) C57-Control cells show co-expression of both IKKα and K5 in each cell. (D) Observe that in the C57-N- IKKα cells, most cells express IKKα in the nucleus (green) and do not express K5 (asterisks), and on the contrary, those scarce cells that do not express nuclear IKKα express K5 (arrows). (E) Both, IKKα and K5, are co-expressed in almost all C57-C-IKKα cells, although sporadically it can be observed the presence of cells that express IKKα in the cytoplasm but do not express K5 (asterisks). Scale bars: 35 μm.
Ijms 23 01375 g005
Ijms 23 01375 g006 550
Figure 6. Induction of MMP9 and c-Myc expression in PDVC57 cells expressing ectopic IKKα. (A,B) WBs of total protein extracts from C57-Control and C57-C- and-N-IKKα cells showing that the levels of MMP9 (A) and c-Myc (B) are increased in both type of cells that express the exogenous IKKα protein.
Figure 6. Induction of MMP9 and c-Myc expression in PDVC57 cells expressing ectopic IKKα. (A,B) WBs of total protein extracts from C57-Control and C57-C- and-N-IKKα cells showing that the levels of MMP9 (A) and c-Myc (B) are increased in both type of cells that express the exogenous IKKα protein.
Ijms 23 01375 g006
Ijms 23 01375 g007 550
Figure 7. Increased survival capacity of C57-N-IKKα cells in a stressful situation. (A–C) Representative experiment of the appearance of cells after 7 days of growth in the absence of serum. Observe the diminished number of C57-Control cells (an average of 2.3 × 106 ± 0.4 × 106 cells/p100) versus 6.5 × 106 ± 0.4 × 106 and 7.9 × 106 ± 1.2 × 106 of C57-C-IKKα and C57-N-IKKα cells/p100, respectively (D) Graphical representation of the number of cells that survive after 7 days of growth in the absence of serum (*** p < 0.001; data are mean ± SEM; by t-test). Scale bars: 50 μm. (E) WB of total protein extracts from C57-Control and C57-C- and-N-IKKα cells showing the induction of the survival proteins Akt and Bcl2 in the C57 cells that express the ectopic IKKα and the lower than control amount of the pro-apoptotic cleaved-Caspase 3 (CC3) in both C57-C-IKKα and C57-N-IKKα cells.
Figure 7. Increased survival capacity of C57-N-IKKα cells in a stressful situation. (A–C) Representative experiment of the appearance of cells after 7 days of growth in the absence of serum. Observe the diminished number of C57-Control cells (an average of 2.3 × 106 ± 0.4 × 106 cells/p100) versus 6.5 × 106 ± 0.4 × 106 and 7.9 × 106 ± 1.2 × 106 of C57-C-IKKα and C57-N-IKKα cells/p100, respectively (D) Graphical representation of the number of cells that survive after 7 days of growth in the absence of serum (*** p < 0.001; data are mean ± SEM; by t-test). Scale bars: 50 μm. (E) WB of total protein extracts from C57-Control and C57-C- and-N-IKKα cells showing the induction of the survival proteins Akt and Bcl2 in the C57 cells that express the ectopic IKKα and the lower than control amount of the pro-apoptotic cleaved-Caspase 3 (CC3) in both C57-C-IKKα and C57-N-IKKα cells.
Ijms 23 01375 g007
Ijms 23 01375 g008 550
Figure 8. Effect of apigenin on C57 skin carcinoma cells of the three genotypes. (A,B) Apigenin treatment causes cell growth inhibition in C57 cells of the three genotypes. Percentage of cells of the three genotypes at the indicated times in the absence or presence of 10 µM (A) and 20 µM (B) of apigenin at the indicated hours of treatment. Observe that treatment with both doses of apigenin causes minimal changes in the viability of the cells after 24 h of treatment; at 48 h, 20 µM of apigenin caused a reduction of cell viability (p < 0.0001); at 72 h of treatment a marked reduction in cell viability was detected with both doses of apigenin tested in the C57 cells of the three genotypes (*** p < 0.001; **** p < 0.0001). Data are shown as mean ± SEM by t-test.
Figure 8. Effect of apigenin on C57 skin carcinoma cells of the three genotypes. (A,B) Apigenin treatment causes cell growth inhibition in C57 cells of the three genotypes. Percentage of cells of the three genotypes at the indicated times in the absence or presence of 10 µM (A) and 20 µM (B) of apigenin at the indicated hours of treatment. Observe that treatment with both doses of apigenin causes minimal changes in the viability of the cells after 24 h of treatment; at 48 h, 20 µM of apigenin caused a reduction of cell viability (p < 0.0001); at 72 h of treatment a marked reduction in cell viability was detected with both doses of apigenin tested in the C57 cells of the three genotypes (*** p < 0.001; **** p < 0.0001). Data are shown as mean ± SEM by t-test.
Ijms 23 01375 g008
Ijms 23 01375 g009 550
Figure 9. Apigenin inhibits the expression of cytoplasmic but not nuclear IKKα protein. Impact of apigenin on the expression other tumoral marker proteins. (A,B) WB showing the changes induced by 10–40 µM of apigenin in C57 cells of the three genotypes after 48 h of treatment. (A) WB showing that apigenin inhibits the expression of the exogenous IKKα localized in the cytoplasm of C57-C-IKKα cells, as well as the endogenous IKKα. (B) WB showing that apigenin diminishes the levels of endogenous IKKα in both C57-Control and C57-N-IKKα cells upon 48 h of treatment with either 10, 20 or 40 µM of apigenin, but does not affect exogenous IKKα localized in the nucleus. Apigenin also attenuates the expression of Cyclin D1, Bcl2 and Akt proteins and increases the cleaved-Caspase-3; a faint attenuation of P-p65 was noticed in the three types of C57 cells (A,B). Since C57-N-IKKα cells express increased levels of the transgene, and to allow comparison of the expression of IKKα in the same blot, the amount of total protein extracts loaded was 20 µg in the case of C57-N-IKKα cells and 50 µg of C57-Control and C57-C-IKKα cells. (C) qPCR analysis of the expression of mouse IKKα mRNA in C57-Control and C57-C-and-N-IKKα. Note that apigenin does not inhibit the expression of the endogenous IKKα at transcriptional level. Cells were incubated in the absence or presence of 10–40 µM apigenin for 48 h. (D) qPCR analysis of the expression of mouse Snail1 mRNA in C57-Control and C57-C-and-N-IKKα cells in the presence or absence of apigenin 20 µM. Observe that apigenin does not inhibit the increased expression of Snail1 in the C57-N-IKKα cells. Data are shown as mean ± SEM; * p < 0.05 by two-tailed unpaired t test with Welch’s correction.
Figure 9. Apigenin inhibits the expression of cytoplasmic but not nuclear IKKα protein. Impact of apigenin on the expression other tumoral marker proteins. (A,B) WB showing the changes induced by 10–40 µM of apigenin in C57 cells of the three genotypes after 48 h of treatment. (A) WB showing that apigenin inhibits the expression of the exogenous IKKα localized in the cytoplasm of C57-C-IKKα cells, as well as the endogenous IKKα. (B) WB showing that apigenin diminishes the levels of endogenous IKKα in both C57-Control and C57-N-IKKα cells upon 48 h of treatment with either 10, 20 or 40 µM of apigenin, but does not affect exogenous IKKα localized in the nucleus. Apigenin also attenuates the expression of Cyclin D1, Bcl2 and Akt proteins and increases the cleaved-Caspase-3; a faint attenuation of P-p65 was noticed in the three types of C57 cells (A,B). Since C57-N-IKKα cells express increased levels of the transgene, and to allow comparison of the expression of IKKα in the same blot, the amount of total protein extracts loaded was 20 µg in the case of C57-N-IKKα cells and 50 µg of C57-Control and C57-C-IKKα cells. (C) qPCR analysis of the expression of mouse IKKα mRNA in C57-Control and C57-C-and-N-IKKα. Note that apigenin does not inhibit the expression of the endogenous IKKα at transcriptional level. Cells were incubated in the absence or presence of 10–40 µM apigenin for 48 h. (D) qPCR analysis of the expression of mouse Snail1 mRNA in C57-Control and C57-C-and-N-IKKα cells in the presence or absence of apigenin 20 µM. Observe that apigenin does not inhibit the increased expression of Snail1 in the C57-N-IKKα cells. Data are shown as mean ± SEM; * p < 0.05 by two-tailed unpaired t test with Welch’s correction.
Ijms 23 01375 g009
Table
Table 1. Oligonucleotides sequences used for the quantitative analysis of the expression of Snail1, mouse IKKα and Vimentin genes.
Table 1. Oligonucleotides sequences used for the quantitative analysis of the expression of Snail1, mouse IKKα and Vimentin genes.
OligonucleotidesSequence
Snail1 (forward)CTTGTGTCTGCACGACCTGT
Snail1 (reverse)GGAGCAGGAGAATGGCTTC
mIKKα (forward)CCCTCCAGTATCAGCATGGC
mIKKα (reverse)GTGCTAACGTCTCTCACACA
Vimentin (forward)CCAACCTTTTCTTCCCTGAAC
Vimentin (reverse)TTGAGTGGGTGTCAACCAGA
TBP (forward)GGGAGAATCATGGACCAGAA
TBP (reverse)GATGGGAATTCCAGGAGTCA
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

García-García, V.A.; Alameda, J.P.; Page, A.; Mérida-García, A.; Navarro, M.; Tejero, A.; Paramio, J.M.; García-Fernández, R.A.; Casanova, M.L. IKKα Induces Epithelial–Mesenchymal Changes in Mouse Skin Carcinoma Cells That Can Be Partially Reversed by Apigenin. Int. J. Mol. Sci. 2022, 23, 1375. https://doi.org/10.3390/ijms23031375

AMA Style

García-García VA, Alameda JP, Page A, Mérida-García A, Navarro M, Tejero A, Paramio JM, García-Fernández RA, Casanova ML. IKKα Induces Epithelial–Mesenchymal Changes in Mouse Skin Carcinoma Cells That Can Be Partially Reversed by Apigenin. International Journal of Molecular Sciences. 2022; 23(3):1375. https://doi.org/10.3390/ijms23031375

Chicago/Turabian Style

García-García, Verónica A., Josefa P. Alameda, Angustias Page, Antonio Mérida-García, Manuel Navarro, Adrián Tejero, Jesús M. Paramio, Rosa A. García-Fernández, and M. Llanos Casanova. 2022. "IKKα Induces Epithelial–Mesenchymal Changes in Mouse Skin Carcinoma Cells That Can Be Partially Reversed by Apigenin" International Journal of Molecular Sciences 23, no. 3: 1375. https://doi.org/10.3390/ijms23031375

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop