miR-622在胃癌细胞中的表达及其功能的研究

目的 研究miR-622在胃癌细胞中的表达,探讨miR-622在胃癌中的生物学功能.方法 采用实时荧光定量PCR检测miR-622在胃癌细胞中的表达,以胃癌细胞SGC-7901和NCI-N87为模型瞬时转染miR-622寡核苷酸前体或抑制体,通过克隆形成、侵袭和划痕实验验证其在胃癌细胞中的功能.结果 荧光定量PCR实验结果表明:miR-622在胃癌细胞SGC-7901中相对表达量为1.29±0.58,而在NCI-N87细胞中相对表达量为10.96±1.02.在SGC-7901细胞中转染了miR-622 寡核苷酸前体,克隆形成率为76％.划痕试验中愈合能力为(11±7)μm,胃癌细胞侵袭能力为(732±3)个,与对照组相比差异均有统计学意义(均P＜0.05).结论 miR-622能够促进胃癌细胞克隆形成、迁移和侵袭.

Expression and biological function of miR-622 in gastric cancer cells

Objective To investigate the biological function of miR-622 in human gastric cancer cell lines of SGC-7901 and NCI-N87 cells and its role in gastric carcinogenesis.Methods We analyzed the expression of miR-622 in those human gastric cancer cell lines by quantitative real-time polymerase chain reaction.Tumorigenesis,migration and invasion ability of miR-622 overexpression was assessed in vitro with miR-622 precursor and inhibitor in in SGC-7901 and NCI-N87 cells.Results The expression level of miR-622 in SGC 7901 was 1.29 ± 0.57,and it was 10.96 ± 1.02 in NCI-N87 cells.The soft agar colony formation rate was 76％ in SGC-7901 after transfecting miR-331-3p precursor,the ability of scratch healing was ( 11 ±7) μm,and the ability of transwell invasion was (731 ±3),compared with that in control group,the differences were statistically significant ( P ＜ 0.05 ).Conclusions Over-expression of miR-622 promotes tumorigenesis,migration,and invasion in gastric cancer cells in vitro.