Department of Gastrointestinal Surgery, the Fourth Affiliated Hospital of China Medical University, Shenyang, 110032, China.
Department of Obstetrics and Gynecology, the Shengjing Affiliated Hospital of China Medical University, Shenyang, 110004, China.
Cancer Med. 2018 Mar;7(3):776-787. doi: 10.1002/cam4.1204. Epub 2018 Feb 21.
This study aims to observe the expression of microRNA (miR)-634 in different gastric cancer cell lines and tissues, and to study the effects of miR-634 on the proliferation, migration, and invasion of the gastric cancer cells. The miR-634 mimics and miR-634 inhibitors were transfected by lentivirus into human gastric cancer SGC-7901 and MGC-803 cells, and the miR-634 cells without transfection were used as the control group (NC group). The expression of miR-634 in the transfected cells was detected by qRT-PCR. Cell viability was measured by the CCK8 assay. The migration and invasion ability of the cells were detected by scratch assays and Transwell chamber assays, respectively, and the luciferase assay verified the binding of miR-634 to the target gene JAG1. The expression level of miR-634 in gastric cancer tissues and cell lines was significantly lower than that in normal adjacent tissues and control cells. The survival of cells was significantly decreased, and number of cells migrating and invading was decreased in the miR-634 mimics group. However, in the miR-634 inhibitor group, the opposite results were observed. Over-expression of miR-634 inhibited the proliferation, migration, and invasion of gastric cancer cell lines, and the miR-634 target gene was JAG1.
本研究旨在观察微小 RNA(miR)-634 在不同胃癌细胞系和组织中的表达,并研究 miR-634 对胃癌细胞增殖、迁移和侵袭的影响。通过慢病毒将 miR-634 模拟物和 miR-634 抑制剂转染入人胃癌 SGC-7901 和 MGC-803 细胞中,未转染 miR-634 的细胞作为对照组(NC 组)。通过 qRT-PCR 检测转染细胞中 miR-634 的表达。通过 CCK8 测定法测量细胞活力。通过划痕实验和 Transwell 室实验分别检测细胞的迁移和侵袭能力,并用荧光素酶实验验证 miR-634 与靶基因 JAG1 的结合。胃癌组织和细胞系中 miR-634 的表达水平明显低于正常相邻组织和对照细胞。miR-634 模拟物组细胞的存活率明显降低,迁移和侵袭的细胞数量减少。然而,在 miR-634 抑制剂组中观察到相反的结果。miR-634 的过表达抑制了胃癌细胞系的增殖、迁移和侵袭,miR-634 的靶基因是 JAG1。