SOX7 is down-regulated in lung cancer

被引:57
作者
Hayano, Takahide [1 ]
Garg, Manoj [1 ]
Yin, Dong [2 ,3 ]
Sudo, Makoto [1 ]
Kawamata, Norihiko [2 ,3 ]
Shi, Shuo [4 ,5 ]
Chien, Wenwen [1 ]
Ding, Ling-wen [1 ]
Leong, Geraldine [1 ]
Mori, Seiichi [6 ,7 ]
Xie, Dong [4 ,5 ]
Tan, Patrick [1 ,8 ]
Koeffler, H. Phillip [1 ,2 ,3 ,9 ]
机构
[1] NUS, Canc Sci Inst Singapore, Genom Oncol Programme, Singapore 117599, Singapore
[2] Cedars Sinai Med Ctr, Dept Hematol & Oncol, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[4] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Nutr Sci, Key Lab Nutr & Metab, Shanghai 200031, Peoples R China
[5] Chinese Acad Sci, Grad Sch, Shanghai 200031, Peoples R China
[6] Japanese Fdn Canc Res, Inst Canc, Div Canc Genom, Tokyo 1358550, Japan
[7] Koto Ward, Tokyo 1358550, Japan
[8] Duke NUS Grad Med Sch, Duke NUS Affiliat Canc & Stem Cell Biol, Singapore 169857, Singapore
[9] Natl Univ Singapore Hosp, Natl Univ Canc Inst, Singapore 119228, Singapore
基金
英国医学研究理事会;
关键词
CNAG; SNP-Chip; Lung cancer; SOX7; Promoter methylation; CELLS; PROGENITORS; EXPRESSION;
D O I
10.1186/1756-9966-32-17
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: SOX7 is a transcription factor belonging to the SOX family. Its role in lung cancer is unknown. Methods: In this study, whole genomic copy number analysis was performed on a series of non-small cell lung cancer (NSCLC) cell lines and samples from individuals with epidermal growth factor receptor (EGFR) mutations using a SNP-Chip platform. SOX7 was measured in NSCLC samples and cell lines, and forced expressed in one of these lines. Results: A notable surprise was that the numerous copy number (CN) changes observed in samples of Asian, non-smoking EGFR mutant NSCLC were nearly the same as those CN alterations seen in a large collection of NSCLC from The Cancer Genome Atlas which is presumably composed of predominantly Caucasians who often smoked. However, four regions had CN changes fairly unique to the Asian EGFR mutant group. We also examined CN changes in NSCLC lines. The SOX7 gene was homozygously deleted in one (HCC2935) of 10 NSCLC cell lines and heterozygously deleted in two other NSCLC lines. Expression of SOX7 was significantly downregulated in NSCLC cell lines (8/10, 80%) and a large collection of NSCLC samples compared to matched normal lung (57/62, 92%, p= 0.0006). Forced-expression of SOX7 in NSCLC cell lines markedly reduced their cell growth and enhanced their apoptosis. Conclusion: These data suggest that SOX7 is a novel tumor suppressor gene silenced in the majority of NSCLC samples.
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页数:11
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