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Article

The Long Non-Coding RNA MIR503HG Enhances Proliferation of Human ALK-Negative Anaplastic Large-Cell Lymphoma

by
Po-Shuan Huang
1,
I-Hsiao Chung
1,
Yang-Hsiang Lin
1,2,
Tzu-Kang Lin
3,
Wei-Jan Chen
4 and
Kwang-Huei Lin
1,2,5,*
1
Department of Biochemistry, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan
2
Liver Research Center, Chang Gung Memorial Hospital, Linkou, Taoyuan 333, Taiwan
3
Neurosurgery, Fu Jen Catholic University Hospital and School of Medicine, Fu Jen Catholic University, New Taipei City 24250, Taiwan
4
Cardiovascular Division, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan 333, Taiwan
5
Research Center for Chinese Herbal Medicine, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333, Taiwan
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(5), 1463; https://doi.org/10.3390/ijms19051463
Submission received: 5 April 2018 / Revised: 10 May 2018 / Accepted: 12 May 2018 / Published: 14 May 2018
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
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Abstract

:
Anaplastic lymphoma kinase (ALK)-negative anaplastic large-cell lymphoma (ALCL) is a rare type of highly malignant, non-Hodgkin lymphoma. Currently, only a few gene rearrangements have been linked to ALK-negative ALCL progression. However, the specific molecular mechanisms underlying the growth of ALK-negative ALCL tumors remain unclear. Here, we investigated aberrantly expressed, long non-coding RNAs (lncRNAs) in ALK-negative ALCL and assessed their potential biological function. MIR503HG (miR-503 host gene) was highly expressed in ALK-negative cell lines and was significantly upregulated in tumors in mice formed from ALK-negative ALCL cell lines. Depletion of MIR503HG suppressed tumor cell proliferation in vivo and in vitro; conversely, its overexpression enhanced tumor cell growth. MIR503HG-induced proliferation was mediated by the induction of microRNA-503 (miR-503) and suppression of Smurf2, resulting in stabilization of the tumor growth factor-β receptor (TGFBR) and enhanced tumor cell growth. Collectively, these findings support a potential role for MIR503HG in cancer cell proliferation through the miR-503/Smurf2/TGFBR axis and indicate that MIR503HG is a potential marker in ALK-negative ALCL.

1. Introduction

Anaplastic lymphoma kinase (ALK)-negative anaplastic large cell lymphoma (ALCL) is a highly malignant non-Hodgkin lymphoma of CD30-positive T-cells that lacks chromosomal rearrangements of the ALK gene encoding a receptor tyrosine kinase [1,2,3]. The Nucleophosmin (NPM)-ALK fusion protein resulting from translocation involving the ALK gene on 2p23, as well as the oncogenic role of these fusion proteins, has been studied extensively in ALK-positive ALCL [4,5,6]. In contrast, the pathogenic mechanism of ALK-negative ALCL is poorly understood. Moreover, it is difficult to distinguish ALK-negative ALCL from other CD30-positive peripheral T-cell lymphomas (PTCLs) because genetic biomarkers are lacking. Ferreri et al. reported that survival rates are higher in patients with ALK-positive ALCL than in ALK-negative patients [7]. Recent studies have also shown that ALK-negative ALCL is a genetically heterogeneous disease whose outcome varies widely depending on genetic subtype [8]. Therefore, identifying an effective marker is necessary for early diagnosis and treatment of ALK-negative ALCL.
Long non-coding RNAs (lncRNAs) are transcripts longer than 200 nucleotides in length that do not encode a protein. Several lncRNAs that are aberrantly expressed in tumors have been reported to play an important role in cancer [9,10,11]. Clinically, lncRNAs associated with survival or prognosis are potential therapeutic targets [12]. However, the clinical significance of lncRNA expression in ALK-negative ALCL development is largely unclear. A previous study identified aberrantly expressed lncRNAs in ALCL specimens using oligonucleotide arrays. We have investigated these overexpressed lncRNAs for their potential function in ALCL progression, focusing on the top five non-coding genes (fold change > 3.5): BMS1P20, LINC01013, MIR503HG, RNF144A-AS1 and CACNA1G-AS1 [13].
Transforming growth factor β (TGF-β) signaling pathways are important in the regulation of cellular proliferation, migration, angiogenesis, and survival [14]. TGF-β ligands have been used as diagnostic, prognostic or predictive markers for many different cancers, including lymphoma [15]. TGF-β signaling is mediated by its cognate receptor, transforming growth factor beta receptor (TGFBR), a transmembrane serine/threonine kinase. Interaction of TGF-β with the receptor leads to phosphorylation and activation of TGFBR, resulting in stimulation of the SMADs signal pathway [16].
In this study, we investigated the role of lncRNAs in regulating proliferative activity and explored underlying molecular mechanisms in ALK-negative ALCL. We found that the potential lncRNA MIR503HG, a host gene of the microRNA miRNA-503, was highly expressed in tumors induced in mice by ALK-negative ALCL cells compared with those formed from ALK-positive ALCL cells. Accordingly, we hypothesized that the functions of MIR503HG are associated with cancer progression. Specifically, our in vitro and in vivo analyses revealed that MIR503HG, which has not been linked to human ALK-negative ALCL, is overexpressed in ALK-negative ALCL cell lines and is significantly upregulated in tumor specimens from mice harboring ALK-negative ALCL tumors.

2. Results

2.1. High Expression of MIR503HG in ALK-Negative ALCL Is Associated with Tumor Proliferation

To identify aberrantly expressed lncRNAs and establish their functional correlation with ALK-negative (FePD, MAC-1) and ALK-positive (SR-786, KARPAS) ALCL cell lines, we performed proliferation assays. Notably, we found that MIR503HG was highly expressed in faster-growing ALK-negative cell lines compared with ALK-positive cell lines (Figure 1a,b). Tumors from nude mice subcutaneously injected with ALK-negative cells were increased in size (Figure 1c) and showed higher expression levels of MIR503HG (Figure 1d) compared with ALK-positive cells. Collectively, these results confirm that MIR503HG is highly expressed in ALK-negative ALCL, suggesting a possible role for MIR503HG in ALK-negative ALCL cell growth.

2.2. MIR503HG Depletion Suppresses ALK-Negative ALCL Proliferation In Vitro and In Vivo

To determine whether MIR503HG is capable of affecting cell proliferation in ALK-negative ALCL cells, we first established MIR503HG-knockdown and control MAC-1 cells. We found that proliferation was significantly decreased in MIR503HG-depleted MAC-1 cells (Figure 2a). Moreover, tumors formed in vivo from MIR503HG-depleted MAC-1 cells subcutaneously injected in nude mice were decreased in size (Figure 2b) and showed lower expression levels of MIR503HG compared with controls (Figure 2c). These features were recapitulated in MIR503HG-depleted FePD cells (Figure 2d) and tumor-bearing nude mice (Figure 2e,f).

2.3. MIR503HG Depletion Acts through Suppression of miR-503 to Promote Degradation of the TGF-β Receptor In Vitro and In Vivo

To further identify the potential mechanism underlying MIR503HG regulation of ALK-negative cell proliferation, we analyzed tumors induced in nude mice by the injection of MIR503HG-depleted MAC-1 or FePD cells. Cao et al. previously reported that the E3 ubiquitin-protein ligase Smurf2 is a target of miR-503 [17]. Notably, tumors formed from MIR503HG-depleted MAC-1 or FePD cells exhibited a significant decrease in the levels of miR-503 (Figure 3a,b) as well as TGFBR and c-Myc (a downstream target of TGFBR signaling) compared with controls; effects that were accompanied by an increase in Smurf2 expression (Figure 3c,d) and ubiquitination-dependent, proteasome-mediated TGFBR degradation (Figure 3e,f). Similar results were obtained for MIR503HG-depleted MAC-1 and FePD cells in vitro (Figure 3g–l). Together, these data indicate that induction of miR-503 by MIR503HG may serve to protect TGFBR from Smurf2-mediated ubiquitination and subsequent degradation.

2.4. MIR503HG Overexpression Promotes ALK-Positive ALCL Growth In Vitro and In Vivo

To further assess the effect of MIR503HG on ALK-positive ALCL cell proliferation, we established MIR503HG-overexpressing SR-786 and control cell lines. Notably, MIR503HG-overexpressing SR-786 cells displayed significantly increased proliferation compared with control cells (Figure 4a). Similarly, nude mice subcutaneously injected with MIR503HG-overexpressing SR-786 cells showed increased tumor size (Figure 4b), as well as higher expression levels of MIR503HG (Figure 4c) compared with those injected with control cells. Similar results were observed in MIR503HG-overexpressing KARPAS cells (Figure 4d) and corresponding tumor-bearing nude mice (Figure 4e,f).

2.5. MIR503HG Overexpression Acts through Induction of miR-503 to Stabilize TGFBR and Enhance Cell Proliferation In Vitro and In Vivo

To further confirm the specific mechanism by which MIR503HG regulates ALK-positive cell proliferation, we analyzed tumor specimens from nude mice injected with MIR503HG-overexpressing SR-786 or KARPAS cells. Notably, tumors formed from MIR503HG-overexpressing cells exhibited a significant increase in miR-503 (Figure 5a,b), TGFBR, and c-Myc (Figure 5c,d) expression levels. However, Smurf2 expression was decreased (Figure 5c,d) compared with that in control groups. Similar results were obtained with MIR503HG-overexpressing SR-786 and KARPAS cells in vitro (Figure 5e–h). Together, these findings indicate that MIR503HG may protect TGFBR from Smurf2-mediated ubiquitination and subsequent proteasome-dependent degradation. Collectively, these results support the conclusion that MIR503HG promotes lymphoma cell proliferation in ALK-negative ALCL through the miR-503/Smurf2/TGFBR pathway (Figure 6).

3. Discussion

Our data indicate that MIR503HG plays an oncogenic role in ALK-negative ALCL by inducing miR-503 expression; this increase in miR-503 leads to Smurf2 degradation and TGFBR stabilization and promotes cell proliferation. The specific pathways involved in ALK-negative ALCL proliferation and the pivotal role of aberrantly expressed MIR503HG in ALK-negative ALCL was validated using an in vivo mouse model. We further found that high expression of MIR503HG in ALK-negative ALCL specimens is associated with faster cell growth. Both gain- and loss-of-function strategies clearly demonstrated that MIR503HG induces proliferation of ALK-negative ALCL cells in vitro and in vivo.
A number of reports have indicated that lncRNAs regulate gene expression through multiple mechanisms at both transcriptional and posttranscriptional levels, including through RNA splicing and epigenetic regulation [18]. Notably, it has been reported that more than 18% of non-protein–coding genes are associated with cancer through unknown functions/mechanisms [19], highlighting the importance of understanding the role of lncRNAs in different cancers. Many abnormally expressed lncRNAs have been reported as potential biomarkers or targets of multiple cancer therapies [20]. In this context, our findings suggest that MIR503HG can be used as a novel oncogenic/proliferation marker for ALK-negative ALCL.
Recent studies of ALK-positive ALCL development have focused on NPM1-ALK translocation and pathogenesis [21,22]. Such ALK fusion proteins exhibit aberrant tyrosine kinase activity that enhances cell proliferation and survival [23]. In contrast, the mechanism underlying progression in ALK-negative ALCL, which lacks the NPM1-ALK fusion protein, has remained largely unknown. Several studies have demonstrated the presence of chromosomal rearrangements of DUSP22 or TP63, overexpression of ERBB4, and mutation of JAK1/STAT3 in ALK-negative ALCL [24].
MIR503HG is a lncRNA that maps to chromosome X (Xq26), a region enriched for genes associated with human reproduction. A recent study reported that MIR503HG is highly expressed in the placenta and other reproductive tissues and may play a role in human reproduction and tumorigenesis [25,26]. Expression levels of miR-503, an miRNA that neighbors MIR503HG on the chromosome, are increased in several cancer cell types and are positively correlated with those of MIR503HG [25,27,28,29]. In the current study, we found that MIR503HG-induced proliferation was mediated by activation of miR-503, but the detailed mechanism is still unclear. To our knowledge, no studies to date have reported an association between MIR503HG and ALK-negative ALCL progression and involvement of a MIR503HG-mediated pathway in ALK-negative ALCL proliferation.
Smurf2 is an E3 ubiquitin ligase that regulates TGF-β signaling [30]. Previous studies have shown that Smurf2 suppresses the TGFBR via ubiquitin-mediated degradation in cancer cells [31]. Moreover, Smurf2 is directly suppressed by miR-503, thereby promoting tumor progression [32]. However, no reports have linked the regulation of lncRNA with the miR-503/Smuf2/ TGFBR pathway in ALK-negative ALCL. The current study showed that MIR503HG enhances the growth ability of ALK-negative ALCL by protecting and activating components of the miR-503/Smuf2/ TGFBR pathway. Collectively, our findings provide novel insight into the role of MIR503HG in lymphoma progression and identify a new potential therapeutic target in ALK-negative ALCL.

4. Materials and Methods

4.1. Mouse Xenograft Model

ALCL cells (1 × 106 cells/200 μL) were injected subcutaneously into the flanks of immunodeficient nude mice. After 2 months, tumor tissues were collected for RNA extraction. At least 2–6 mice per group were used in all animal experiments. Animal experimental protocols (IACUC Approval No: CGU13-105; Period of Protocol: valid from 08/01/2014–07/31/2017) were reviewed and approved by the National Laboratory Animal Center (NLAC). All experiments were performed in accordance with the relevant guidelines and regulations of the Laboratory Animal Center of Chang Gung University, and all efforts were made to minimize animal pain.

4.2. Quantitative Reverse Transcription-Polymerase Chain Reaction

Total RNA was collected using the TRIzol reagent (Life Technologies Inc., Carlsbad, CA, USA) and reverse transcribed into cDNA using a Superscript II kit (Life Technologies, Karlsruhe, Germany). MIR503HG expression levels were measured by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) using a Real-Time ABI PRISM 7500 system (Applied Biosystems, Foster City, CA, USA). MIR503HG was detected using the forward primer MIR503HG-F (5′-AAGGAATCCTCTCCCACCATTT-3′) and reverse primer MIR503HG-R (5′-ACT CAT TTG GCG GGA AAA C-3′). A single unique sequence corresponding to MIR503HG (NCBI Reference Sequence: NR_024607.1 [33]) was detected. MIR503HG levels were normalized to those of 18S ribosomal RNA (18S rRNA). miR-503-5p was detected using miRNA-specific stem-loop reverse transcription primer (miR-503-5p: 5′-CTCAACTGGTGTCGTGGAGTCGGCAATTCAGTTGAGCTG CAGAA-3′) in miRNA real-time reactions. miR-503-5p expression was subsequently detected using the specific primer miR-503-5p-F (5′-CGGCGGTAGCAGCGGGAACAGT-3′) and universal reverse primer Universal-R (5′-CTGGTGTCGTGGAGTCGGCAATTC-3′). Values were normalized to those of RNU6B (U6 snRNA).

4.3. Cell Culture

Human ALK-positive (SR-786, KARPAS) and negative (MAC-1, FePD) ALCL cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS) at 37 °C in a humidified 5% CO2 incubator.

4.4. Immunoblotting

Protein concentrations were determined using a Bradford-based method (Pierce Biotechnology, Rockford, IL, USA). Equal amounts of protein (80 μg/lane) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) on 8–10% gels (Tris Buffer 1.5 M pH 8.8; Biotools Co., Ltd., Taipei, Taiwan). Separated proteins were transferred to a nitrocellulose membrane (pH 7.9; Amersham Biosciences Inc., Piscataway, NJ, USA) and incubated with different primary antibodies, including anti-Smurf2 (ab53316, Abcam, Cambridge, UK), anti- TGFBR (ab124894, Abcam, Cambridge, UK) and anti-c-Myc (ab32072, Abcam, Cambridge, UK).

4.5. Establishment of Stable MIR503HG-Knockdown Cell Lines

MIR503HG short hairpin RNAs (shRNAs) were purchased from the National RNAi Core Facility (Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan). Stable MIR503HG-knockdown MAC-1 and FePD cell lines infected with lentivirus expressing shRNA against MIR503HG were established by culturing cells in selection medium consisting of DMEM/10% FBS containing puromycin (0.3 μg/mL).

4.6. Establishment of Stable MIR503HG-Overexpressing Cell Lines

An MIR503HG expression plasmid was obtained by PCR-amplifying MIR503HG using the specific primers 5′-CGCTGGTACCGAAGGTAGAAGGTGGGGTC-3′ (forward) and 5′-CGCGCTCGAGTAACGGAAATCAAAAGCAGC-3′ (reverse) and cloning the resulting PCR product into the pcDNA3 vector. MIR503HG-overexpressing SR-786 and KARPAS cell lines were established by first transfecting cells with the resulting MIR503HG expression plasmid using the Lipofectamine reagent (Invitrogen, Waltham, MA, USA). After 24 h, stably expressing cells were selected by culturing transfected cells in the presence of G418 (800 μg/mL). Expression levels of MIR503HG RNA were determined by qRT-PCR.

4.7. Proliferation Assay

Cell proliferation was evaluated by seeding cells at 5 × 104 cells and then counting cell numbers after several days using a hemocytometer.

4.8. Ubiquitination Assay

Whole-cell lysates were extracted after treating cells for 4 h with the proteasome inhibitor MG132 (10 mM). Non-specific binding was eliminated by first incubating cell lysates with protein A/G (Santa Cruz Biotechnology, Santa Cruz, CA, USA) for 1 h, after which lysates were incubated with anti- TGFBR antibody (Abcam, Biotech, Life Science; ab124894) overnight at 4 °C. The next day, lysates were incubated with protein A/G for 1 h at 4 °C. Ubiquitinated TGFBR signals were detected with an anti-ubiquitin antibody (Epitomics Inc., Burlingame, CA, USA).

4.9. Statistical Analysis

Data are presented as means ± SEMs of at least three experiments. Statistical analyses were performed using Student’s t test or one-way analysis of variance (one-way ANOVA). Where suitable, a Mann–Whitney U or Fisher’s exact test was used; a Kruskal–Wallis test or Pearson’s χ2 test was used for comparisons of more than two groups. Spearman’s rank correlation coefficient was used to assess correlations of two different examinations.

Author Contributions

P.S.H., I.H.C. and Y.H.L. performed the experiments, T.K.L. and W.J.C. provided experimental materials, K.H.L. study designed and wrote the manuscript. P.S.H. and I.H.C. contributed equally to this work.

Acknowledgments

This work is supported by grants from the Chang Gung Memorial Hospital (CMRPG3G0381 to T.K.L. and CRRPD1F0012, CRRPD1F0013, NMRPD1G0941, NMRPD1G0951, MOST106-2320-B-182-031-MY3, 106-2320-B-182-032-MY3 to K.H.L.).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Identification of MIR503HG in anaplastic lymphoma kinase (ALK)-negative anaplastic large-cell lymphoma (ALCL). (a) The cell growth ability of ALK-positive (SR-786 or KARPAS) and ALK-negative (FePD or MAC-1) cell lines was tested. (b) Expression levels of MIR503HG were measured by q-RT-PCR. (c) Tumors from nude mice subcutaneously injected with ALK-positive or -negative cells were photographed. (d) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
Figure 1. Identification of MIR503HG in anaplastic lymphoma kinase (ALK)-negative anaplastic large-cell lymphoma (ALCL). (a) The cell growth ability of ALK-positive (SR-786 or KARPAS) and ALK-negative (FePD or MAC-1) cell lines was tested. (b) Expression levels of MIR503HG were measured by q-RT-PCR. (c) Tumors from nude mice subcutaneously injected with ALK-positive or -negative cells were photographed. (d) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
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Figure 2. MIR503HG depletion suppresses ALK-negative ALCL growth. (a) Proliferation ability was analyzed in MIR503HG-depleted (MIR503HG-KD#1 or KD#2) and control (Luc#1 or Luc#2) MAC-1 cells. (b) Tumors from nude mice subcutaneously injected with MIR503HG-depleted or control MAC-1 cells were photographed. (c) MIR503HG expression levels, determined by qRT-PCR. (d) Proliferation of FePD cells, assayed under conditions similar to those for MAC-1 cells. (e) Tumors from nude mice injected with MIR503HG-depleted or control FePD cells were photographed. (f) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
Figure 2. MIR503HG depletion suppresses ALK-negative ALCL growth. (a) Proliferation ability was analyzed in MIR503HG-depleted (MIR503HG-KD#1 or KD#2) and control (Luc#1 or Luc#2) MAC-1 cells. (b) Tumors from nude mice subcutaneously injected with MIR503HG-depleted or control MAC-1 cells were photographed. (c) MIR503HG expression levels, determined by qRT-PCR. (d) Proliferation of FePD cells, assayed under conditions similar to those for MAC-1 cells. (e) Tumors from nude mice injected with MIR503HG-depleted or control FePD cells were photographed. (f) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
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Figure 3. MIR503HG depletion promotes degradation of TGFBR. (a,b) MIR503HG and miR-503 expression levels were determined by qRT-PCR in specimens of tumors from nude mice injected with MIR503HG-depleted (KD#1 or KD#2) or control (Luc#1 or Luc#2) MAC-1 (a) or FePD (b) cells. (c,d) Smurf2, TGFBR, and c-Myc expression levels were determined. (e,f) Immunoprecipitation assays of specimens of tumors from nude mice injected with MIR503HG-depleted or control MAC-1 (e) and FePD (f) cells; ubiquitinated TGFBR was analyzed by Western blotting. (g,h) MIR503HG and miR-503 expression levels in MAC-1 (g) and FePD (h) cell lines were determined by q-RT-PCR under similar conditions. (i,j) Smurf2, TGFBR, and c-Myc expression levels in these cell lines were determined. (k,l) Immunoprecipitation assays of MIR503HG-depleted and control MAC-1 (k) and FePD (l) cells; ubiquitinated TGFBR was analyzed by Western blotting. Differences were analyzed using a Kruskal-Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
Figure 3. MIR503HG depletion promotes degradation of TGFBR. (a,b) MIR503HG and miR-503 expression levels were determined by qRT-PCR in specimens of tumors from nude mice injected with MIR503HG-depleted (KD#1 or KD#2) or control (Luc#1 or Luc#2) MAC-1 (a) or FePD (b) cells. (c,d) Smurf2, TGFBR, and c-Myc expression levels were determined. (e,f) Immunoprecipitation assays of specimens of tumors from nude mice injected with MIR503HG-depleted or control MAC-1 (e) and FePD (f) cells; ubiquitinated TGFBR was analyzed by Western blotting. (g,h) MIR503HG and miR-503 expression levels in MAC-1 (g) and FePD (h) cell lines were determined by q-RT-PCR under similar conditions. (i,j) Smurf2, TGFBR, and c-Myc expression levels in these cell lines were determined. (k,l) Immunoprecipitation assays of MIR503HG-depleted and control MAC-1 (k) and FePD (l) cells; ubiquitinated TGFBR was analyzed by Western blotting. Differences were analyzed using a Kruskal-Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
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Figure 4. MIR503HG overexpression promotes growth of ALK-positive ALCL cells. (a) Proliferation ability was analyzed in MIR503HG-overexpressing (MIR503HG#1 or MIR503HG#2) and control (Ctr#1 or Ctr#2) SR-786 cells. (b) Tumors from nude mice subcutaneously injected with MIR503HG-overexpressing or control SR-786 cells were photographed. (c) MIR503HG expression levels, determined by qRT-PCR (d) Proliferation assays of KARPAS cells performed under similar conditions. (e) Tumors from nude mice injected with MIR503HG-overexpressing or control KARPAS cells were photographed. (f) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
Figure 4. MIR503HG overexpression promotes growth of ALK-positive ALCL cells. (a) Proliferation ability was analyzed in MIR503HG-overexpressing (MIR503HG#1 or MIR503HG#2) and control (Ctr#1 or Ctr#2) SR-786 cells. (b) Tumors from nude mice subcutaneously injected with MIR503HG-overexpressing or control SR-786 cells were photographed. (c) MIR503HG expression levels, determined by qRT-PCR (d) Proliferation assays of KARPAS cells performed under similar conditions. (e) Tumors from nude mice injected with MIR503HG-overexpressing or control KARPAS cells were photographed. (f) MIR503HG expression levels, determined by qRT-PCR. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
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Figure 5. MIR503HG overexpression acts through induction of miR-503 to stabilize TGFBR and enhance cell proliferation. (a,b) MIR503HG and miR-503 expression levels in specimens of tumors from nude mice injected with MIR503HG-overexpressing (MIR503HG#1 or MIR503HG#2) or control SR-786 and KARPAS cells were determined by qRT-PCR. (c,d) Smurf2, TGFBR, and c-Myc expression levels were determined by Western blotting. (e,f) MIR503HG and miR-503 expression levels were determined by qRT-PCR in SR-786 and KARPAS cell lines under similar conditions. (g,h) Smurf2, TGFBR, and c-Myc expression levels in these cell lines were determined by Western blotting. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
Figure 5. MIR503HG overexpression acts through induction of miR-503 to stabilize TGFBR and enhance cell proliferation. (a,b) MIR503HG and miR-503 expression levels in specimens of tumors from nude mice injected with MIR503HG-overexpressing (MIR503HG#1 or MIR503HG#2) or control SR-786 and KARPAS cells were determined by qRT-PCR. (c,d) Smurf2, TGFBR, and c-Myc expression levels were determined by Western blotting. (e,f) MIR503HG and miR-503 expression levels were determined by qRT-PCR in SR-786 and KARPAS cell lines under similar conditions. (g,h) Smurf2, TGFBR, and c-Myc expression levels in these cell lines were determined by Western blotting. Differences were analyzed using a Kruskal–Wallis test (* p < 0.05). Data are presented as means ± SEMs of at least three experiments.
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Figure 6. MIR503HG promotes ALK-negative ALCL proliferation. Schematic depiction of MIR503HG promotion of ALK-negative ALCL proliferation through activation of the miR-503/Smurf2/TGFBR cascade. LncRNA MIR503HG is highly expressed in ALK-negative cells compared with ALK-positive ALCL cells. Concomitantly, miR-503 (its host gene MIR503HG) is stimulated, decreasing its target Smurf2 (an E3 ubiquitin ligase) and consequently stabilizing TGFBR, thereby inducing c-Myc expression and subsequent cell proliferation. (→: induces)
Figure 6. MIR503HG promotes ALK-negative ALCL proliferation. Schematic depiction of MIR503HG promotion of ALK-negative ALCL proliferation through activation of the miR-503/Smurf2/TGFBR cascade. LncRNA MIR503HG is highly expressed in ALK-negative cells compared with ALK-positive ALCL cells. Concomitantly, miR-503 (its host gene MIR503HG) is stimulated, decreasing its target Smurf2 (an E3 ubiquitin ligase) and consequently stabilizing TGFBR, thereby inducing c-Myc expression and subsequent cell proliferation. (→: induces)
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Huang, P.-S.; Chung, I.-H.; Lin, Y.-H.; Lin, T.-K.; Chen, W.-J.; Lin, K.-H. The Long Non-Coding RNA MIR503HG Enhances Proliferation of Human ALK-Negative Anaplastic Large-Cell Lymphoma. Int. J. Mol. Sci. 2018, 19, 1463. https://doi.org/10.3390/ijms19051463

AMA Style

Huang P-S, Chung I-H, Lin Y-H, Lin T-K, Chen W-J, Lin K-H. The Long Non-Coding RNA MIR503HG Enhances Proliferation of Human ALK-Negative Anaplastic Large-Cell Lymphoma. International Journal of Molecular Sciences. 2018; 19(5):1463. https://doi.org/10.3390/ijms19051463

Chicago/Turabian Style

Huang, Po-Shuan, I-Hsiao Chung, Yang-Hsiang Lin, Tzu-Kang Lin, Wei-Jan Chen, and Kwang-Huei Lin. 2018. "The Long Non-Coding RNA MIR503HG Enhances Proliferation of Human ALK-Negative Anaplastic Large-Cell Lymphoma" International Journal of Molecular Sciences 19, no. 5: 1463. https://doi.org/10.3390/ijms19051463

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