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中国应用生理学杂志 ›› 2021, Vol. 37 ›› Issue (4): 402-406.doi: 10.12047/j.cjap.6090.2021.041

• 研究论文 • 上一篇    下一篇

Mir-335-5p靶向G6PD对结肠癌细胞增殖、凋亡的影响

樊小群, 李欢, 朱华雄, 黄健平, 何吕芬   

  1. 海南省三亚市人民医院检验科, 三亚 572000
  • 出版日期:2021-07-28 发布日期:2021-08-09
  • 通讯作者: Tel: 15091971615; E-mail: rz1ikx1@163.com

Effects of miR-335-5p targeting G6PD on proliferation and apoptosis of colon cancer cells

FAN Xiao-qun, LI Huan, ZHU Hua-xiong, HUANG Jian-ping, HE Lyu-fen   

  1. Department ofLaboratory, Sanya People's Hospital, Sanya 572000, China
  • Online:2021-07-28 Published:2021-08-09

摘要: 目的: 探讨Mir-335-5p通过靶向G6PD对结肠癌细胞增殖、凋亡的影响。方法: 设置正常结肠细胞组、空白对照组、NC组、miRNA-335-5p mimic组;体外培养结肠上皮细胞(IEC)和人源性结肠癌细胞SW480,并对NC组、miRNA-335-5p mimic组细胞进行转染;采用RT-qPCR检测各组细胞中miR-335-5p及G6PD mRNA表达水平;双荧光素酶报告实验验证Mir-335-5p对G6PD靶向作用;MTT实验检测各组细胞的增殖;流式细胞术检测转染后各组细胞凋亡率;Western blot检测G6PD及凋亡蛋白Bax、Bcl-2、caspase3相对表达水平。结果: 与正常结肠细胞相比,空白对照组、NC组结肠癌细胞SW480细胞中miR-335-5p相对表达水平降低,G6PD mRNA相对表达水平升高(P<0.05);与空白对照组、NC组相比,miR-335-5p mimic组细胞miR-335-5p表达水平明显升高,G6PD mRNA表达水平显著降低(P<0.05)。与空白对照、NC组相比,miR-335-5p mimic组结肠癌SW480细胞生长活性显著降低,凋亡率显著升高(P<0.05)。miR-335-5p mimic+WT-G6PD 3′-UTR组的荧光素酶相对活性低于miR-335-5p NC+WT-G6PD 3′-UTR组(P<0.05)。与空白对照组相比,miR-335-5p mimic组细胞中G6PD、Bcl-2蛋白相对表达水平显著降低,Bax、caspase3蛋白表达水平显著升高(P<0.05)。结论: Mir-335-5p可能通过靶向G6PD抑制结肠癌细胞增殖、促进凋亡。

关键词: microRNA-335-5p, 6-磷酸葡萄糖脱氢酶, 结肠癌, 细胞增殖, 细胞凋亡

Abstract: Objective: To investigate the effects of miR-335-5p targeting glucose-6-phosphate dehydrogenase (G6PD) on the proliferation and apoptosis of colon cancer cells. Methods: Normal colon cell group, blank control group, NC group and miRNA-335-5p mimic group were set up. Colonic epithelial cells (IEC) and human colon cancer cells SW480 were cultured in vitro, and the cells in the NC group and miRNA-335-5p mimic group cells were transfected. RT-qPCR was used to detect the expression levels of miR-335-5p and G6PD mRNA in each group of cells. The targeting effect of miR-335-5p on G6PD was verified by Double Luciferase Report experiment. MTT assay was used to detect cell proliferation. Flow cytometry was used to detect the apoptosis rate. The expressions of G6PD, Bax, Bcl-2 and caspase-3 were detected by Western blot. Results: Compared with normal colon cells, the relative expression levels of miR-335-5p in SW480 cells of colon cancer in the blank control group and NC group were decreased, and the relative expression level of G6PD mRNA was increased (P<0.05); compared with the blank control group and NC group, the expression level of miR-335-5p in miR-335-5p mimic group was increased significantly, and the expression of G6PD mRNA was decreased significantly (P<0.05). Compared with the blank control group and NC group, the proliferative activity of colon cancer SW480 cells in miR-335-5p mimic group was decreased significantly, and the apoptosis rate was increased significantly (P<0.05). The relative activity of luciferase in miR-335-5p mimic + WT-G6PD 3 '- UTR group was lower than that in miR-335-5p NC + WT-G6PD 3' - UTR group (P<0.05). Compared with the blank control group, the relative expression levels of G6PD and bcl-2 protein in miR-335-5p mimic group were decreased significantly, and the expression levels of Bax and caspase-3 protein were increased significantly (P<0.05). Conclusion: MiR-335-5p may inhibit the proliferation and promote apoptosis of colon cancer cells by targeting G6PD.

Key words: microRNA-335-5p, glucose-6-phosphate dehydrogenase, colon cancer, cell proliferation, apoptosis

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