首页 | 本学科首页   官方微博 | 高级检索  
检索        

miR-183-5p/mTOR信号轴介导有氧糖酵解促进 胃癌细胞增殖
引用本文:王溪,冯利,杨文渊,卢洪胜,姜知财,黄桔秀.miR-183-5p/mTOR信号轴介导有氧糖酵解促进 胃癌细胞增殖[J].中国现代医生,2023,61(3):24-27.
作者姓名:王溪  冯利  杨文渊  卢洪胜  姜知财  黄桔秀
作者单位:台州市中心医院(台州学院附属医院)全科医学科,浙江台州 318000;浙江省台州医院内分泌科,浙江台州 318000;台州市中心医院(台州学院附属医院)消化内科,浙江台州 318000;浙江省椒江区白云街道社区卫生服务中心全科医学科,浙江台州 318000
基金项目:台州市科学技术局项目(22ywb32)
摘    要:目的 探讨miR-183-5p/mTOR信号轴是否通过影响胃癌细胞有氧糖酵解过程而促进胃癌细胞增殖,为胃癌的治疗提供新靶点。方法 使用转染试剂盒对MGC-803胃癌细胞进行inhibitor NC、miR-183-5p inhibitor、mimics NC、miR-183-5p mimics转染;葡萄糖、乳酸、腺嘌呤核苷三磷酸(adenosine triphosphate,ATP)检测试剂盒检测低葡萄糖、乳酸、ATP水平变化;通过蛋白质印迹和聚合酶链反应(polymerase chain reaction,PCR)检测雷帕霉素机械靶蛋白(mechanistic target of rapamycin,mTOR)mRNA、葡萄糖转运蛋白(glucose transporter 1,GLUT1)和乳酸脱氢酶(recombinant lactate dehydrogenase A,LDHA)蛋白;二苯基四氮唑溴盐法(multiple table tournament,MTT)检测MGC-803胃癌细胞活性。结果 与inhibitor NC组相比,miR-183-5p inhibitor在胃癌细胞中低表达(P<0.001),与mimics NC组相比,miR-183-5p inhibitor组在胃癌细胞中高表达miR-183-5p(P<0.0001);过表达miR-183-5p可促进MGC-803胃癌细胞对葡萄糖的消耗(P<0.01),生成更多的乳酸和ATP(P<0.01)、上调LDHA和GLUT1蛋白(P<0.01)、促进mTOR mRNA表达、促进胃癌细胞增殖。结论 miR-183-5p/mTOR信号轴通过调控有氧糖酵解相关蛋白表达促进MGC-803胃癌细胞增殖。

关 键 词:有氧糖酵解  miR-183-5p  雷帕霉素机械靶蛋白  葡萄糖转运蛋白  乳酸脱氢酶  增殖

miR-183-5p/mTOR signaling axis mediates the effect of aerobic glycolysis on the proliferation of gastric cancer cells
Abstract:Objective To investigate whether miR-183-5p/mTOR signaling axis regulates the proliferation of gastric cancer cells by affecting the process of aerobic glycolysis, and to provide a new target for the treatment of gastric cancer. Methods MGC-803 gastric cancer cells were transfected with inhibitor NC, miR-183-5p inhibitor, mimics NC and miR-183-5p mimics using transfection kit. Glucose, lactic acid and ATP detection kits were used to detect the changes of low glucose, lactic acid and ATP levels. mTOR mRNA, GLUT1 and LDHA proteins were detected by WB and PCR. The activity of MGC-803 gastric cancer cells was detected by MTT assay. Results Compared with the inhibitor NC group, the expression of miR-183-5p inhibitor was down-regulated in gastric cancer cells (P<0.001). miR-183-5p inhibitor significantly increased the expression of miR-183-5p in gastric cancer cells (P<0.0001), indicated that the transfection was successful. Overexpression of miR-183-5p promoted glucose consumption of MGC-803 gastric cancer cells (P<0.01), produced more lactate and ATP (P<0.01), up-regulated LDHA and GLUT1 proteins (P<0.01), promoted mTOR mRNA expression, and promoted the proliferation of gastric cancer cells. Conclusion miR-183-5p /mTOR signaling axis affects the proliferation of MGC-803 gastric cancer cells by regulating the expression of aerobic glycolytic related proteins.
Keywords:
点击此处可从《中国现代医生》浏览原始摘要信息
点击此处可从《中国现代医生》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号