Xu Ruizhe, Guo Qi, Zhao Peifeng, Lu Haiyan, Zhang Bo
Department of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Institute of Radiation Oncology, Soochow University, Suzhou, China.
Evid Based Complement Alternat Med. 2022 Sep 30;2022:6946051. doi: 10.1155/2022/6946051. eCollection 2022.
GAGE12I is a tumor metastasis-promoting factor, which can induce gastric cancer cells to invade and migrate. We investigated the effect of miR-28-5p targeting GAGE12I on proliferation, invasion, and migration of human gastric cancer cell lines SGC-7901, AGS, and MGC-803. The expression levels of miR-28-5p and GAGE12I were detected by real-time PCR and western blot, respectively. Cell proliferation, migration, and invasion were measured by MTT and Transwell chamber. The interaction between miR-28-5p and GAGE12I was investigated by bioinformatics analysis and luciferase assay. Results showed that the expression of miR-28-5p in human gastric cancer cell lines was lower than that in normal gastric epithelial cells ( < 0.05). Overexpression of miR-28-5p suppressed cell proliferation, invasion, and migration ( < 0.05). GAGE12I was confirmed as a target of miR-28-5p. Cell proliferation, invasion, and migration were decreased in cells transfected with shGAGE12I compared with those of the scrambled group ( < 0.05). Collectively, miR-28-5p negatively regulated GAGE12I and reduced the proliferation, invasion, and migration of gastric cancer cells.
GAGE12I是一种促进肿瘤转移的因子,可诱导胃癌细胞侵袭和迁移。我们研究了靶向GAGE12I的miR-28-5p对人胃癌细胞系SGC-7901、AGS和MGC-803增殖、侵袭和迁移的影响。分别通过实时PCR和蛋白质印迹法检测miR-28-5p和GAGE12I的表达水平。通过MTT和Transwell小室检测细胞增殖、迁移和侵袭。通过生物信息学分析和荧光素酶测定研究miR-28-5p与GAGE12I之间的相互作用。结果显示,人胃癌细胞系中miR-28-5p的表达低于正常胃上皮细胞(<0.05)。miR-28-5p的过表达抑制细胞增殖、侵袭和迁移(<0.05)。GAGE12I被证实为miR-28-5p的靶标。与乱序组相比,转染shGAGE12I的细胞中细胞增殖、侵袭和迁移减少(<0.05)。总体而言,miR-28-5p负向调节GAGE12I并降低胃癌细胞的增殖、侵袭和迁移。