首页|miR29c下调S100A4蛋白表达参与人胃癌细胞增殖促进凋亡

miR29c下调S100A4蛋白表达参与人胃癌细胞增殖促进凋亡

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目的 探讨miR-29c对人胃腺癌细胞增殖、凋亡的影响及其与转移相关蛋白S100A4的关系.方法 采用细胞培养人胃癌细胞系BGC-823、SGC-7901和人正常胃粘膜上皮GES-1细胞,应用qRT-PCR检测各株细胞miR29c的表达.用hsa-miR29c-mimics类似物(miR29c组),hsa-miR29c-inhibitor(阴性对照组)分别转染BGC-823细胞,空白对照组加入转染液,用CCK8及MTT法检测细胞增殖,流式细胞术检测细胞凋亡,Western blot检测S100A4相关肿瘤相关蛋白的表达.结果 与正常胃粘膜上皮细胞GES-1表达率(1.131±0.069)相比,MiR-29c在胃癌细胞BGC823(0.254±0.025),SGC-7901(0.466±0.057)(F=57.5,P<0.05).BGC823细胞转染miR29c模拟物后MiR-29c的表达量为:4.126±0.231,0.405±0.174,0.557±0.102,差异具有统计学意义(F=850.1,P<0.05).转染24h、48h、72h后,MiR-29c组细胞的OD450值分别为:1.074±0.127、1.609±0.178、2.008±0.104;阴性对照组为:0.419±0.169、0.477±0.092、0.738±0.153,空白对照组为:0.830±0.305.其中,转染48h、72h后,MiR-29c组明显高于对照组(F=59.46,P<0.05).细胞转染24h后,miR29c组细胞凋亡率分别是(6.900±0.414)%、(4.490±0.316)%、(3.850±0.243)%,,阴性对照组凋亡率分别是(10.830±0.231)%、(11.940±0.279)%、(13.530±0.941)%,空白对照组凋亡率分别是:(10.190±0.188)%、(11.76±0.569)%、(13.260±0.987),(P<0.001).各组S100A4蛋白的表达分别为0.770±0.028、1.109±0.083、1.024±0.042,(P=0.0021).结论 miR29c在胃癌细胞系中表达降低,通过抑制S100A4抑制人胃癌细胞增殖并促进胃癌细胞凋亡.
MiR-29c downregulated and regulated cell proliferation and apoptosis by suppression S100A4 in human gastric carcinoma cell lines
Objective To explore the effect of MicroRNA-29c(miR29c)on the proliferation and apoptosis of human gastric adeno-carcinoma cell lines,and to explore the relationship between miR29c and S100A4 metastasis-related protein.Methods The human gastric carcinoma cell lines BGC-823,SGC-7901 and normal gastric mucosa epithelial GES-1 cell line were cultured in carbon diox-ide incubator.The expreesion of miR29c in cell lines were tested by qRT-PCR method.BGC-823 cells were transfected with hsa-miR29c-mimics analogs(miR29c group)and hsa-miR29c-inhibitor(negative control group),respectively.In the control group,trans-fer solution was added,cell proliferation was detected by CCK8 and MTT,cell apoptosis was detected by flow cytometry.The expres-sion of S100A4-associated tumor-associated protein was detected by Western Blot.Results Compared with the expression rate of GES-1 in normal gastric mucosa epithelial cells(1.131±0.069),the expression rate of MiR-29c in gastric cancer cells BGC823(0.254±0.025),SGC-7901(0.466±0.057)(F=57.5,p<0.05).The expression of MiR-29c in BGC823 cells transfected with miR29c mimics was 4.126±0.231,0.405±0.174,0.557±0.102,and the differences were statistically significant(F=850.1,p<0.05).After transfection for 24h,48h and 72h,the OD450 values of miR29c group cells were 1.074±0.127,1.609±0.178 and 2.008±0.104,respectively.The negative control group was 0.419±0.169,0.477±0.092,0.738±0.153,and the control group was 0.830±0.305.After transfection for 48h and 72h,MiR-29c group was significantly higher than control group(F=59.46,p<0.05).After transfection for 24h,the apoptosis rates of miR29c group were(6.900±0.414)%,(4.490±0.316)%,(3.850±0.243)%,respectively.The apoptosis rates of the negative control group were(10.830±0.231)%,(11.940±0.279)%and(13.530±0.941)%,respectively.The apoptosis rates of the blank control group were:(10.190±0.188)%,(11.76±0.569)%,(13.260±0.987),(p<0.001).The expression of S100A4 protein in each group was 0.770±0.028,1.109±0.083,1.024±0.042,respectively(p=0.0021).Conclusion MiR29c can inhibit proliferation and induced apoptosis in hu-man gastric carcinoma cell lines through suppress S100A4 protein expression.

Gastric carcinomamiR29cProliferationApoptosisS100A4

李鹏、刘光世、李涛

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新疆维吾尔自治区人民医院胃肠外科诊疗中心胃肠肿瘤外科,乌鲁木齐 830001

胃癌 MiR-29c 增殖 凋亡 S100A4

新疆维吾尔自治区人民医院科技引进创新项目新疆维吾尔自治区卫生健康青年医学科技人才专项

20160307WJWY-202122

2024

新疆医学
新疆维吾尔自治区医学会

新疆医学

影响因子:0.385
ISSN:1001-5183
年,卷(期):2024.54(7)