Cell-based chemical fingerprinting identifies telomeres and lamin A as modifiers of DNA damage response in cancer cells

Telomere maintenance by telomerase activity supports the infinite growth of cancer cells. MST-312, a synthetic telomerase inhibitor, gradually shortens telomeres at non-acute lethal doses and eventually induces senescence and apoptosis of telomerase-positive cancer cells. Here we report that MST-312 at higher doses works as a dual inhibitor of telomerase and DNA topoisomerase II and exhibits acute anti-proliferative effects on cancer cells and xenografted tumours in vivo. Our cell-based chemical fingerprinting approach revealed that cancer cells with shorter telomeres and lower expression of lamin A, a nuclear architectural protein, exhibited higher sensitivity to the acute deleterious effects of MST-312, accompanied by formation of telomere dysfunction-induced foci and DNA double-strand breaks. Telomere elongation and lamin A overexpression attenuated telomeric and non-telomeric DNA damage, respectively, and both conferred resistance to apoptosis induced by MST-312 and other DNA damaging anticancer agents. These observations suggest that sufficient pools of telomeres and a nuclear lamina component contribute to the cellular robustness against DNA damage induced by therapeutic treatment in human cancer cells.

Telomeres are protective structures at the ends of eukaryotic linear chromosomes that consist of telomeric DNA, (TTAGGG)n, and binding proteins, such as shelterin 1 . Telomeric DNA has a single-stranded 3′-overhang that forms a protective t-loop structure 2 . Because the DNA polymerase-dependent replication machinery cannot replicate the ends of linear DNAs (the end replication problem), telomeres shorten after each round of DNA replication. Critically shortened telomeres lose the ability to form the t-loop structure and are then recognised as deleterious DNA double-strand breaks 3 . This condition leads to a block in DNA replication and cell division, resulting in a permanent growth arrest, called replicative senescence. Thus, in normal cells, telomere shortening and the accompanying inhibition of cell division blocks the growth of cells and functions as a tumour suppressor mechanism 4 . In contrast, dysfunction of telomeres can drive genomic instability, which can facilitate tumour progression 5 .
In vast majority of human cancer cells, the end replication problem is solved by the maintenance of telomeres by the telomerase enzyme 6 , which consists of the hTERT catalytic subunit and the RNA template (called hTR or hTERC, in humans). While hTR is ubiquitously expressed in broad ranges of tissues, hTERT is the limiting factor for telomerase activity 7 . Recent cancer genome analyses have identified hTERT promoter mutations that lead to elevated transcriptional activation of the gene in many cancers 8,9 . These cancer cells harbouring mutations in Results MST-312 inhibits human cancer cell growth in mouse xenograft models. Non-acute cytotoxic doses of the telomerase inhibitor MST-312 shorten telomeres and induce senescence and apoptosis of telomerase-positive human leukaemia and solid tumour cells 14,16 . Meanwhile, MST-312 at higher doses promptly inhibits the proliferation of leukaemia cells 14 . To examine the in vivo antitumour efficacy of MST-312, we subcutaneously injected human breast cancer HBC-4 cells into nude mice and treated mice with various doses of MST-312 through various routes. In non-treated and vehicle-treated mice, the tumours grew extensively ( Fig. 1A-C). In contrast, intratumoural, intravenous or oral administration of MST-312 at the maximum tolerated or lower doses retarded tumour growth. In mice receiving oral administration of 400 mg/kg MST-312, while a maximum 16.7% body weight loss was observed at day 56, the body weight recovered and returned to levels higher than the original body weight at day 82 (Fig. 1C). Reduction in body-weight was less than 10% during the course of treatments in case of the intratumoural ( Telomere Fingerprint Database reveals a correlation between shorter telomeres and higher susceptibility to MST-312-induced acute cell growth inhibition. To explore the acute anti-proliferative effects of MST-312, we used a human cancer cell line panel that consists of 39 cell lines derived from various tissues (JFCR39) 28 . Each cell line was treated with various concentrations of MST-312 for 48 h and the anti-proliferative effects were determined (Fig. 1D). The average GI 50 value of the 39 cell lines was 4.7 μM. The GI 50 deviation from the average was calculated for each cell line and aligned in a fingerprint (Fig. 1E).
To analyse the relationship between MST-312 sensitivity and telomere status, we quantitated various telomere-related parameters, including the single-stranded (i.e., G-tail/3′-overhang) and the double-stranded telomere length (Fig. 1F); the protein expression for shelterin components (TRF1, TRF2, POT1, TPP1, RAP1, TIN2), DNA damage response factors (RIF1, MRE11, RAD50, NBS1, 53BP1, PARP-1), tankyrase and its binding proteins (TNKS1BP1, NuMA), RecQ helicases (WRN, BLM) and other related proteins (Fig. 1G); telomerase activity ( Fig. 1H); and hTERT gene expression (Fig. 1I, column 9 from the left). Two-dimensional hierarchical clustering grouped several factors according to their functional relevance (Fig. 1I). For example, components for the MRN complex, MRE11, NBS1 and RAD50 (light blue dots), were classified into the same cluster. In addition, four of six shelterin components, TRF1, POT1, TIN2 and TPP1 (orange dots), were within the same cluster, whereas the other two direct binding components, TRF2 and RAP1 (pink dots), were closely bound. Another larger cluster contained hTERT, telomerase activity, and its binding protein dyskerin (yellow dots). These observations suggest that our newly constructed telomere fingerprint database might be able to predict the relative intensity of the physical or functional interaction between various combinations of the fingerprints. There was no significant similarity between the fingerprints of MST-312 and telomere-related parameters. For example, while MST-312 is a telomerase inhibitor, the cell sensitivity to this compound did not correlate with telomerase activity (r = −0.094, P = 0.582) or hTERT mRNA expression (r = 0.131, P = 0.439) ( Supplementary Fig. S1A,B).
When three cell lines, DMS114, NCI-H23 and LOX-IMVI, which possess very long telomeres [more than 20 kb, designated as super long telomere (SLT) type cells] (Fig. 1F), were excluded, we found that acute sensitivity to MST-312 correlated with the length of the double-stranded telomere DNA (Fig. 1J). The cells with shorter telomeres tended to be more susceptible to the acute deleterious effect of MST-312. Furthermore, among the cell lines with very short telomeres (i.e., the mean TRF length is less than 4 kb), there was an inverse correlation between telomerase activity and MST-312 sensitivity (r = −0.826, P = 0.0415, Supplementary Fig. S1C).
We further examined the effect of MST-312 on lung cancer NCI-H522 and A549 cells, which retain short and long telomeres with a mean telomeric restriction fragment (TRF) length of 3.2 kb and 9.6 kb, respectively. The GI 50 values for MST-312 in NCI-H522 and A549 cells were 1.4 μM and 4.6 μM, respectively. Treatment with 5 μM MST-312 for 48 h induced apoptosis of NCI-H522 more frequently than A549 cells ( Fig. 2A,B). Consistent with these observations, NCI-H522 cells showed enlarged telomere dysfunction-induced foci (TIF) of DNA damage response factors, such as γH2AX, 53BP1, phosphorylated ATM kinase and phosphorylated SMC1, upon treatment with 5 μM MST-312, whereas A549 did not (Fig. 2C,D). MST-312-induced enlarged TIF formation was also observed in another cell line with short telomeres, stomach MKN74 cells (mean TRF length: 3.2 kb), but not in telomerase-independent immortalised, alternative lengthening of telomere (ALT) type GM847 cells, which possess a homologous recombination-based telomere maintenance mechanism 29 (Fig. 2E). Under these short term treatment conditions, telomere shortening was not detectable by Southern blot analysis (Fig. 2F). MST-312 induces DNA double-strand breaks in the drug-sensitive cancer cells. Having confirmed telomere dysfunction upon MST-312 treatment of cells that have short telomeres, we next examined the effect of MST-312 on two SLT type cell lines, DMS114 and NCI-H23. We found that both cell lines were sensitive to MST-312 (GI 50 values: 2.5 μM and 1.9 μM, respectively) even though these cells possess very long telomeres (mean TRF length: > 20 kb). As shown in Fig. 3A,B, MST-312 treatment of these cells caused DNA damage foci that were not colocalised with telomeres. MST-312-resistant colorectal cancer HT-29 cells (GI 50 : 12 μM; mean TRF length: 7.3 kb) did not exhibit foci upon treatment. Consistent with these observations, metaphase spreads of chromosomes showed that MST-312 caused DNA double-strand breaks in MST-312-sensitive cells (NCI-H522, MKN74, DMS114 and NCI-H23) but not in MST-312-resistant cells (A549 and HT-29) (Fig. 3C,D). Furthermore, the telomerase negative (ALT type) GM847 cells also exhibited DNA double-strand breaks in response to MST-312 (Fig. 3D). These results suggest that MST-312 at a higher dose (e.g., 5 μM) than that for telomerase inhibition (~1 μM) can induce DNA double-strand breaks in a telomerase-independent manner.
Then, we next knocked down hTERT in A549 and NCI-H522 cells and evaluated their MST-312 sensitivities. In the absence of MST-312, siRNA-mediated knockdown of hTERT reduced the growth of A549 and NCI-H522 cells to 77% and 58%, respectively, of the non-silencing control siRNA-treated cells. It has been reported that knockdown, instead of enzymatic inhibition, of telomerase exerts such an acute anticancer effect in an enzyme activity-independent manner 30 . We confirmed that this siRNA had no effect on the growth of telomerase-independent GM847 cells, excluding the possibility of an off-target effect (Kyotaro Hirashima and HS, unpublished observation). Under these hTERT-depleted conditions, MST-312 further inhibited the cell growth in a dose-dependent manner ( Supplementary Fig. S1D,E). COMPARE analysis of chemical fingerprints identifies MST-312 as a DNA topoisomerase II inhibitor. The ability of MST-312 to induce DNA damage in GM847 cells suggests that MST-312 has another molecular target in addition to telomerase. To identify potential targets, we performed COMPARE analysis 12,31 using chemical fingerprints of MST-312 and various anticancer compounds. We found that MST-312 has a similar fingerprint to fingerprints of DNA topoisomerase II inhibitors, such as ICRF-193, ICRF-154, TAS-103 and NC190 (Fig. 4A,B). This result prompted us to perform DNA decatenation assays, which monitor DNA topoisomerase II activity to decatenate the kinetoplast DNA. As shown in Fig. 4C, MST-312 inhibited DNA topoisomerase II with an IC 50 value of 2 μM, which was three-fold higher than the IC 50 value for telomerase inhibition 14 . Downregulation of DNA topoisomerase II is a well-established mechanism for resistance to DNA to western blot analyses with indicated primary antibodies. For each antibody blot and Coomassie stain, three different blots or gels were derived from the same experiment and were processed in parallel. Their borders were indicated by dotted lines. Each blot/gel contains NCI-H23 cells as a calibration standard. Full-length blots were presented in Supplementary Fig. S4. (H) Telomerase activity in JFCR39 cells. Cell lysates were prepared and subjected to TRAP assay. Average telomerase activity of all cell lines was defined as zero. (I) Two-dimensional hierarchical cluster analysis of the telomere-related bioparameters. The clustering result was generated by Cluster (ver. 3.0) and Java TreeView (Ver. 1.1.6r4). Orange dots: four of six shelterin components (TRF1, POT1, TIN2 and TPP1); yellow dots: telomerase components (hTERT and Dyskerin) and telomerase activity; pink dots: two shelterin components (TRF2, RAP1); light blue dots: MRN complex (MRE11, NBS1 and RAD50). (J) Correlation between the cell sensitivity to MST-312 and the length of the mean TRF length (left) or telomere signals quantitated by HPA assay (right). In these graphs, the super long telomere cells (NCI-H23, DMS114 and LOX-IMVI) were excluded from the calculation of correlation coefficient. topoisomerase II inhibitors 32 . MST-312 at 150 μM inhibited the growth of Saccharomyces cerevisiae YFK30, a drug-hypersensitive strain 33 (Fig. 4D). In contrast, the DNA topoisomerase II-mutant in the YFK30 background, top2, K414N, was resistant to the growth inhibitory effect of MST-312. In the control treatment, this mutant strain was also resistant to doxorubicin, another DNA topoisomerase II inhibitor. iFISH analysis revealed that DNA topoisomerase II inhibitors, such as ICRF-193, TAS-103 and etoposide, induced non-telomeric DNA damage foci that were distinct from the TIF induced by MST-312 in NCI-H522 cells (Fig. 4E, left panel). While the percentages of the ATM-pS1981 DNA damage focus-positive cells were comparable between the drug-treated cells, the percentages of the TIF-positive cells were significantly higher in MST-312-treated cells than in other drug-treated cells (Fig. 4E, right panel). MST-295, a telomerase inhibitor with telomerase inhibiting activity comparable to MST-312 14 , only marginally inhibited DNA topoisomerase II (Fig. 4F). MST-295 induced TIF and enlarged TIF in NCI-H522 cells, indicating telomerase inhibition (Fig. 4G). However, MST-295 did not induce DNA double-stranded breaks (Fig. 4H). These observations indicate that MST-312 used at 5 μM and higher doses works as a dual inhibitor for telomerase and DNA topoisomerase II and induces telomere dysfunction in cancer cells with short telomeres and non-telomeric DNA damage in cancer cells that do not necessarily have short telomeres.
Lamin A is a functional determinant for MST-312-induced DNA double-strand breaks. As described above, MST-312 did not induce the DNA damage response in some cancer cell lines, such as A549 and HT-29 cells. To identify the functional determinant for the susceptibility to MST-312-induced non-telomeric DNA damage, we performed BIO-COMPARE analysis 34 and examined the similarity between the chemical fingerprint of MST-312 sensitivity and biological fingerprints of protein expression. We found that the expression levels for lamin A, an inner nuclear membrane protein, inversely correlated with MST-312 sensitivity with the highest correlation (r = −0.518, P = 0.0006) (Fig. 5A,B). Meanwhile, there was a weak correlation between expression levels of lamin C, a splicing valiant of LMNA gene, and MST-312 sensitivity (r = −0.389, P = 0.0137) ( Supplementary Fig. S2A). Importantly, SLT-type DMS114, NCI-H23 and LOX-IMVI cells, which retain very long telomeres and are sensitive to MST-312, expressed the lowest levels of lamin A protein. NCI-H522 cells, which retain very short telomeres and are sensitive to MST-312, also expressed very low levels of lamin A. MST-312-resistant cells, such as A549 and HT-29 cells, expressed high levels of lamin A. These expression patterns were confirmed by indirect immunofluorescent staining for lamin A (Fig. 5C).
To examine whether lamin A is functionally involved in the susceptibility to MST-312-induced DNA damage, NCI-H522 cells were infected with retrovirus containing lamin A (LMNA) cDNA and selected with hygromycin (Fig. 5D). The resulting NCI-H522/LMNA cells were treated with 5 μM MST-312 for 48 h and DNA double-stranded breaks were quantitated. As shown in Fig. 5E, lamin A overexpression in NCI-H522 cells reduced the number of MST-312-induced double-stranded breaks. By contrast, lamin C overexpression did not affect the formation of DNA damage foci upon treatment with MST-312 ( Supplementary Fig. S2B). These results suggest that lamin A expression is a functional determinant of the sensitivity to the DNA damage acutely induced by higher doses of MST-312.

Telomere elongation and lamin A expression alleviate MST-312-induced apoptosis.
Because cancer cells with shorter telomeres tended to be more sensitive to MST-312 than cells with longer telomeres (Fig. 1J), we next transfected NCI-H522 or NCI-H522/LMNA cells with an expression vector encoding the telomerase catalytic subunit, hTERT, and upregulated the telomerase activity in the cells (Fig. 6A,B). The resulting NCI-H522/hTERT and NCI-H522/LMNA + hTERT cells exhibited elongated telomeres (Fig. 6C). Immuno-FISH analysis revealed that the telomeric and non-telomeric DNA damage induced by MST-312 were reduced by lamin A and hTERT expression, respectively, and simultaneous overexpression of the two proteins eliminated the DNA damage foci in the nuclei (Fig. 6D-F). Consistent with these observations, expression of either lamin A or hTERT protein reduced the levels of apoptosis induced by MST-312 in NCI-H522 cells, and simultaneous overexpression of both proteins further inhibited apoptosis (Fig. 6G). Lamin A and hTERT also reduced the rates of apoptosis induced by DNA damaging agents, such as cisplatin, camptothecin and etoposide, but not by the anti-microtubule agent paclitaxel (Fig. 6G). These observations indicate that telomere length and lamin A expression are the critical determinants for telomeric and non-telomeric DNA damaging agents.
Lamin A overexpression not only reduced lamin C expression but also slightly reduced telomerase activity (Fig. 6A,B), suggesting the possibility that lamin C expression plays a supportive role for telomerase activity. Then, we reconstituted lamin C expression in NCI-H522/mock and NCI-H522/LMNA cells and quantified the telomerase activity (Supplementary Fig. S3). The results showed that lamin C expression does not enhance telomerase activity in NCI-H522/mock cells (lanes 1/2 and 5/6). Meanwhile, a slight downregulation of telomerase activity in NCI-H522/LMNA cells was marginally rescued by lamin C expression (lanes 3/4 and 7/8). These observations suggest that lamin C supports telomerase activity to some extent, but it is not sufficient to rescue the MST-312-induced double-stranded breaks (Supplementary Fig. S2).

Discussion
In cultured cancer cells, telomerase inhibitors can allow for telomerase shortening, restoring the end replication problem, and inducing eventual telomere crisis 14 . This pharmacological effect is achieved by using intentionally low doses of telomerase inhibitors that would not induce acute cytotoxicity. Here we abandoned the classical idea that telomerase inhibitors should be evaluated at such low doses. As shown in Fig. 1D, treatment with the telomerase inhibitor MST-312 at higher doses exhibited acute anti-proliferative effects. Upon investigating the molecular mechanism for this rapid anticancer effect of MST-312, we found that the compound, when used at high doses, is a dual inhibitor of telomerase and DNA topoisomerase II and can induce telomeric and non-telomeric DNA damage.
Exploiting the telomere fingerprints of 39 human cancer cell lines, we found that cancer cell lines with shorter telomeres are more sensitive to the acute deleterious effects of MST-312. This result makes sense because shorter telomeres would allow fewer numbers of cell division to occur and promptly cause telomere crisis in the absence of telomerase activity. In fact, telomere elongation by overexpression of telomerase (this study) or tankyrase 16 , a positive regulator of telomerase, confers resistance to MST-312. Consistent with these observations, a preclinical study suggested that telomere length could be a predictive biomarker of the telomerase inhibitor imetelstat 35 . Furthermore, a randomised phase II study of imetelstat has demonstrated a trend toward longer median progression-free survival and overall survival in imetelstat-treated patients with non-small cell lung cancer with short telomeres 19 . Intriguingly, cancer cells often maintain shorter telomeres than those in cells in surrounding normal tissues 36,37 , and short telomeres are associated with a less-differentiated status of tumours in vivo 38,39 . In this sense, telomerase inhibitors may be suitable for targeting such malignant tumours.  We cannot precisely quantitate the level of telomerase activity in MST-312-treated cells. Because MST-312 is a reversible telomerase inhibitor, it is washed out during the course of lysate preparation from the drug-treated cells. Accordingly, telomerase activity is restored in the cell lysate 14 . For these reasons, it is difficult to evaluate the relationship between telomerase activity in MST-312-treated cells and their drug sensitivities. Telomerase can be also inhibited by siRNA-mediated knockdown. However, effects of hTERT knockdown and telomerase inhibition are not necessarily equivalent each other and, therefore, it was difficult by the knockdown approach to check if MST-312 sensitivity is partially mediated by the inhibition of telomerase activity. Still, however, MST-312 resistance by hTERT overexpression (Fig. 6) would support that this drug sensitivity is partially mediated by telomerase inhibition.
We have also demonstrated that the expression levels of lamin A protein are inversely correlated with the susceptibility to apoptosis by treatment with MST-312 and DNA damaging anticancer drugs but not by paclitaxel. Lamin A is one of the nuclear matrix proteins and interacts with several proteins, such as LAPs 1A, 1B 40 , emerin 41 , retinoblastoma transcription factor pRB 42 and myne-1 43 . Among these proteins, both emerin and pRB associate with DNA, indicating that lamin A interacts with several DNA-binding proteins and plays important roles in the nucleus. In fact, loss of lamin A function increases the chromatin motion [44][45][46][47] . Mutations in the LMNA gene, which encodes the two nuclear lamins, lamin A and C, produced by alternative splicing, cause a wide range of diseases called laminopathies 48,49 . With regard to the association between senescence and lamin A function, much can be learned about the premature aging syndrome Hutchinson-Gilford progeria syndrome (HGPS) 50,51 . In cases with a splicing mutation of LMNA, the mutant lamin A protein, progerin, accumulates in HGPS patient cells. Progerin has a 50-amino-acid internal deletion and lacks the proteolytic cleavage site necessary to remove the carboxy-terminal 18 amino acids to generate mature lamin A 50,51 . Progerin acts as a dominant negative mutant of lamin A and causes dysregulation of the DNA damage response 48,49,[52][53][54][55] . HGPS patient-derived cells are highly sensitive to ionising radiation-induced DNA damage, and ectopic expression of progerin mimics this phenotype 54 . At the molecular level, progerin traps DNA-dependent protein kinase, a critical protein in double-strand break repair 56 . Loss of wild-type lamin A can also result in perturbed non-homologous end joining and homologous recombination 57 . Our BIO-COMPARE analysis of the JFCR39 panel showed that the expression level of lamin A protein inversely correlates with the sensitivity to various DNA damaging drugs (YM, TY and HS, unpublished observations). These observations support the functional importance of lamin A for proper DNA damage response and repair.
hTERT-mediated immortalisation of HGPS cells improves nuclear morphology, decreases progerin protein levels and diminishes the number of persisting 53BP1 foci, alleviating the dysregulation in the DNA damage response and repair machinery 54 . Furthermore, loss of lamin A alters the nuclear distribution and heterochromatin status of telomeres 58 . These observations suggest a functional linkage between telomeres and lamin A. Consistent with these data, we found that lamin A overexpression in NCI-H522 cells repressed the telomeric DNA damage induced by MST-312 (Fig. 6F).
Our chemical fingerprinting analysis demonstrates that the MST-312 sensitivity profile at the acute phase is similar to the profiles of DNA topoisomerase II inhibitors, especially ICRF-193. One study showed that ICRF-193 preferentially attacks telomeres in a telomeric protein TRF2-dependent manner 59 . However, we found that ICRF-193 or other DNA topoisomerase II inhibitors, which have no telomerase inhibitory activities, induced less telomeric DNA damage than MST-312 (Fig. 4E). Thus, the mixed phenotype of the telomeric and non-telomeric DNA damage would be caused by the dual inhibition of telomerase and DNA topoisomerase II by MST-312 treatment in NCI-H522 cells. Inhibitors with multiple nuclear target, as demonstrated in this study, may suggest new treatment strategies against cancer.
Telomere and telomerase assays. Genomic DNA was isolated and telomere restriction fragments (TRFs) were detected by Southern blot analysis as previously described 38 . The mean length of TRFs was determined with an Atto densitoscan analyser (Tokyo, Japan). All procedures were performed in accordance with the institutional guideline and regulation under approval by the JFCR Radiation Safety Committee. Telomeric DNA signals and the telomeric 3′-overhang were quantitated by HPA assay as described previously 65 . TRAP assay for estimation of telomerase activity was performed as previously described 38 .
RT-PCR. Total RNAs were prepared using the RNeasy Mini kit (Qiagen, Venlo, Netherlands), and hTERT expression was monitored by RT-PCR using Ready-To-Go beads (Amersham Pharmacia, Piscataway, NJ, USA) and a pair of primers, 5′-TTGGTGCACACCGTCTGGAGG-3′ and 5′-CTGGAGGTGCAGAGCGACTAC-3′. The PCR conditions were 29 temperature cycles of 94 °C for 45 sec, 60 °C for 45 sec, and 72 °C for 90 sec. Signals were detected by agarose gel electrophoresis and normalised by β-microglobulin expression, which was detected by primers 5′-ACCCCCACTGAAAAAGATGA-3′ and 5′-ATATTCAAACCTCCATGATG-3′, under conditions of 24 temperature cycles of 94 °C for 30 sec, 55 °C for 1 min and 72 °C for 2 min. In pilot studies, we determined the quantitative range of the reaction by modifying the number of temperature cycle.
DNA topoisomerase II assay. In vitro DNA topoisomerase II assay was performed using the Topo II Assay Kit (TopoGEN, Buena Vista, CO, USA) according to the manufacturer's instructions. In brief, kinetoplast DNA was incubated with 2 units of DNA topoisomerase II for 1 h at 37 °C in the presence of test compounds. DNA decatenation was assessed by agarose gel electrophoresis.
Plasmid transfection and Retroviral infection. pLNCX2/lamin C was generated by amplifying lamin C cDNA from total cDNA of A549 cells as a template and subsequently inserting it into the pLNCX2 vector (BD Biosciences). NCI-H522 cells were transiently transfected pLNCX2 or pLNCX2/lamin C with Lipofectamine 2000 transfection reagent (Thermo Fisher Scientific), according to the manufacturer's instructions. pLNCX2/ hTERT was generated by cloning the hTERT fragment 66 into the pLNCX2 vector. pLHCX/lamin A was generated by cloning the lamin A fragment (Open Biosystems, Cambridge, UK) into the pLHCX vector (BD Biosciences). Amphotropic retroviruses were produced by transfecting the plasmids into Phoenix amphotropic cells using standard calcium phosphate precipitation. NCI-H522 cells were infected with the retrovirus essentially as described 67 . Infected cells were selected with 400 μg/ml of G418 and/or 200 μg/ml of hygromycin and cultured as described 68 . All procedures were performed in accordance with the institutional guideline and regulation under approval by the JFCR Safety Committee for Recombinant DNA Experiments.
SCienTiFiC RepoRts | (2018) 8:14827 | DOI:10.1038/s41598-018-33139-x Statistical analysis. Unpaired t tests were performed for comparison of the groups with and without MST-312 treatment. Tukey-Kramer tests were performed to examine every combination of multiple experimental groups.

Data Availability
The datasets generated and analysed during the current study are available from the corresponding author on reasonable request.