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作 者:刘棣[1] 宋玲琴[1] 张寅斌[1] 闫婉君 赵小瑶 盛倩文 许朋 代志军[1] 康华峰[1] Liu Di;Song Lingqin;Zhang Yinbin;Yan Wanjun;Zhao Xiaoyao;Sheng Qianwen;Xu Peng;Dai Zhijun;Kang Huafeng(Department of Oncology, the Second Affiliated Hospital of Xi'an Jiaotong University, Shaanxi Xi'an 710004, China.)
机构地区:[1]西安交通大学第二附属医院肿瘤科,陕西西安710004
出 处:《现代肿瘤医学》2018年第9期1344-1347,共4页Journal of Modern Oncology
基 金:中央高校基本科研业务费专项资金资助(编号:2014gjhz11);陕西省科技厅重点研发计划一般项目资助(编号:2017SF-172);必康基金(编号:2017BIKANGJIJIN-020);西安交通大学第二附属医院院青年基金[编号:YJ(QN)201305]
摘 要:目的:研究miRNA-141在胃癌细胞中的生物学功能。方法:定量PCR检测人胃黏膜细胞GES-1,胃癌细胞株BGC823、MGC803、SGC7901中miRNA-141的表达,通过miRNA-141 inhibitor、mimics分别抑制及促进miRNA-141的表达,观察癌细胞增殖、克隆形成、侵袭能力的变化。结果:胃癌细胞BGC823、MGC803、SGC7901中miRNA-141处于低表达状态。上调miRNA-141的表达后,miRNA-141明显抑制SGC7901细胞增殖(P<0.05),抑制肿瘤细胞克隆形成(P<0.05)及癌细胞侵袭力(P<0.05)。结论:miRNA-141对胃癌细胞SGC7901具有负性调控作用,可以作为潜在的治疗靶点。Objective: To identify the regulation of miRNA-141 on proliferation of gastric cancer cells. Methods:The expression of miRNA-141 in gastric cancer cell line BGC823,MGC803,SGC7901 were detected by Real-time PCR. The MTT was used to detect SGC7901 cell proliferation after miRNA-141 downregulated and upregulated. The colony forming efficiency of miRNA-141 was detected by colony forming assay. The transwell chamber was used to investigate the influence of miRNA-141 on invasion of SGC7901 cells. Results: miRNA-141 were in downregulated statues in BGC823,MGC803,SGC7901 cell lines. The upregulated miRNA-141 could inhibit proliferation,colony forming and cell invasion( P<0. 05). Also the downregulated miRNA-141 promoted cell proliferation,colony forming and cell invasion( P<0. 05). Conclusion: miRNA-141 negatively regulate gastric cancer cell SGC7901,it is a potential therapy target.
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