MicroRNA-141 confers resistance to cisplatin-induced apoptosis by targeting YAP1 in human esophageal squamous cell carcinoma

被引:91
作者
Imanaka, Yukako
Tsuchiya, Soken [2 ]
Sato, Fumiaki [2 ]
Shimada, Yutaka [3 ]
Shimizu, Kazuharu [2 ]
Tsujimoto, Gozoh [1 ]
机构
[1] Kyoto Univ, Dept Genom Drug Discovery Sci, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Dept Nanobio Drug Discovery, Grad Sch Pharmaceut Sci, Kyoto 6068501, Japan
[3] Toyama Univ, Dept Surg & Sci, Grad Sch Med & Pharmaceut Sci Res, Toyama 930, Japan
关键词
apoptosis; cisplatin resistance; esophageal carcinoma; microRNA; YAP1; YES-ASSOCIATED PROTEIN; EXPRESSION; CANCER; ONCOGENES; SIGNATURES; MODULATE; GENE;
D O I
10.1038/jhg.2011.1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs (miRNAs) are endogenous non-coding RNAs that function as negative regulators of gene expression. Alterations in miRNA expression have been shown to affect tumor growth and response to chemotherapy. In this study, we explored the possible role of miRNAs in cisplatin resistance in esophageal squamous cell carcinoma (ESCC). First we assessed the sensitivity of nine human ESCC cell lines (KYSE series) to cisplatin using an in vitro cell viability assay, and then we compared the miRNA profiles of the cisplatin-sensitive and -resistant cell lines by miRNA microarray analysis. The two groups showed markedly different miRNA expression profiles, and 10 miRNAs were found to be regulated differentially between the two groups. When miR-141, which was the most highly expressed miRNA in the cisplatin-resistant cell lines, was expressed ectopically in the cisplatin-sensitive cell lines, cell viability after cisplatin treatment was increased significantly. Furthermore, we found that miR-141 directly targeted the 3'-untranslated region of YAP1, which is known to have a crucial role in apoptosis induced by DNA-damaging agents, and thus downregulated YAP1 expression. Our study highlights an important regulatory role for miR-141 in the development of cisplatin resistance in ESCC. Journal of Human Genetics (2011) 56, 270-276; doi:10.1038/jhg.2011.1; published online 3 February 2011
引用
收藏
页码:270 / 276
页数:7
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