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出 处:《中华实验外科杂志》2016年第1期93-96,共4页Chinese Journal of Experimental Surgery
摘 要:目的观察微小RNA(miRNA,miR)-31对结肠癌细胞增殖和迁移的影响,并探讨其作用机制。方法采用反转录聚合酶链反应(RT—PCR)的方法检测miR-31在结肠癌细胞株和结直肠癌患者癌组织中的表达,细胞计数试剂盒(CCK-8)法和细胞划痕实验分别检测过表达miR-31后结肠癌细胞增殖和迁移,Western blot检测过表达miR-31的结肠癌细胞中Rasp21蛋白活化子1(RASA1)的表达。结果miR-31在结肠癌组织和细胞中高表达(P〈0.05),过表达miR-31可促进结肠癌细胞的增殖和迁移能力。同时,转染miR-31模拟物组RASA1的相对表达量为0.21±0.05,miR-31抑制剂组的相对表达量为2.464-0.35,两者比较差异有统计学意义(P〈0.05)。结论miR-31对结肠癌细胞的增殖和迁移具有促进作用,其机制与靶向作用于RASA1蛋白有关。Objective To investigate the influence of microRNA (miRNA, miR)-31 on cell proliferation and migration of colorectal cancer. Methods The expression of miR-31 in colorectal cancer tissues and matched adjacent mucosa were measured by reverse transcriptase - polymerase chain reaction ( RT - PCR). Then we detected the cell proliferation and migration of colorectal cancer cell lines transfected by miR-31 mimics. The expression of Ras p21 protein activator 1 (RASA1) coloreetal cancer cell lines transfected by miR-31 mimics were detected by Western blotting. Results MiR-31 in colorectal cancer cell lines and tissues were high-expression. Overexpression of miR-31 in colorectal cancer cell lines could promote cell proliferation and migration. Meanwhile, the expression of RASA1 in miR-31 mimics group was 0. 21± 0. 05, which was significantly higher than that in miR-31 inhibition group ( 2.46 ±0. 35 ). Conclusion miR-31 may participate in the cell proliferation and migration of colorectal cancer cell lines, and the possible mechanism is targeting effect on RASA1.
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