Pei Z J, Zhang Z G, Hu A X, Yang F, Gai Y
Pharmazie. 2017 Jun 1;72(6):344-347. doi: 10.1691/ph.2017.6404.
MicroRNAs (miRNAs) play crucial roles in the development and progression of human cancers, including Gastric cancer (GC). In this study, we investigated the correlation of miR-122-5p expression with cell proliferation, and apoptosis in a GC cell line. GC cells SCG 7901 were transfected with control, miR-122-5p or miR-122-5p inhibitor and MTT assay, western blot, and BrdU staining were respectively used to investigate the effect of miR-122-5p on GC cell cycle. The overexpression of miR-122-5p could reduce cell proliferation in SCG7901 cells, and BrdU staining finally verified miR-122-5p induced cell growth arrest by upregulation p27 expression in SCG7901cells. On the other hand, cells apoptosis research showed that miR-122-5p induced apoptosis by targeting MYC in SCG7901 cells. Finally, in this study, miR-122-5p was confirmed inhibiting tumor GC cells proliferation and inducing cells apoptosis by targeting MYC. All these findings suggest that miR-122-5p may be involved in progression of GC and could be a new therapeutic target for this disease.
微小RNA(miRNA)在包括胃癌(GC)在内的人类癌症的发生和发展中起着至关重要的作用。在本研究中,我们调查了miR-122-5p表达与胃癌细胞系中细胞增殖和凋亡的相关性。用对照、miR-122-5p或miR-122-5p抑制剂转染胃癌细胞SCG 7901,分别采用MTT法、蛋白质免疫印迹法和BrdU染色法研究miR-122-5p对胃癌细胞周期的影响。miR-122-5p的过表达可降低SCG7901细胞的增殖,BrdU染色最终证实miR-122-5p通过上调SCG7901细胞中p27的表达诱导细胞生长停滞。另一方面,细胞凋亡研究表明,miR-122-5p通过靶向SCG7901细胞中的MYC诱导凋亡。最后,在本研究中,证实miR-122-5p通过靶向MYC抑制胃癌细胞增殖并诱导细胞凋亡。所有这些发现表明,miR-122-5p可能参与胃癌的进展,并且可能是该疾病的一个新的治疗靶点。