摘要
目的:探讨miR-647对子宫内膜癌细胞增殖和凋亡的影响及其分子机制。方法:实验设置miR-NC组、miR-647组、anti-miR-NC组、anti-miR-647组、si-NC组、si-NLRC5组、miR-647+pcDNA组、miR-647+pcDNA-NLRC5组。实时荧光定量PCR(quantitative real-time PCR,qRT-PCR)检测miR-647和核苷酸寡聚化域样受体亚家族C5(nucleotide oligomerization domain-like receptor subfamily C5,NLRC5)mRNA表达水平;蛋白质印迹(Western blot)法检测NLRC5、细胞周期蛋白D1(CyclinD1)、细胞周期蛋白依赖性激酶抑制剂1A(p21)、B细胞淋巴瘤/白血病-2(Bcl-2)、Bcl-2相关X蛋白(Bax)的蛋白表达;四甲基偶氮唑盐(MTT)比色法检测细胞活性;流式细胞术检测细胞凋亡;荧光素酶报告实验检测miR-647和NLRC5的靶向关系。结果:子宫内膜癌组织中miR-647低表达,NLRC5高表达(P<0.05);过表达miR-647或抑制NLRC5表达,细胞活性显著降低,细胞凋亡率显著升高,CyclinD1、Bcl-2表达水平显著降低,p21、Bax表达水平显著升高(P<0.05)。miR-647靶向调控NLRC5,NLRC5过表达逆转了miR-647过表达对子宫内膜癌Ishikawa细胞增殖和凋亡的作用。结论:过表达miR-647可能通过靶向下调NLRC5的表达抑制子宫内膜癌细胞增殖,促进细胞凋亡。
Objective:To investigate the effect of miR-647 on the proliferation and apoptosis of endometrial cancer cells and its molecular mechanism.Methods:The experiment set miR-NC group,miR-647 group,anti-miR-NC group,anti-miR-647 group,si-NC group,si-NLRC5 group,miR-647+pcDNA group,miR-647+pcDNA-NLRC5 group.Real-time fluorescence quantitative PCR(RT-qPCR)was used to detect the expression levels of miR-647 and NLRC5 mRNA.Western blot detection of nucleotide oligomerization domain-like receptor subfamily C5(NLRC5),CyclinD1,cyclin-dependent kinase inhibitor 1A(p21),B-cell lymphocytes tumor/leukemia-2(Bcl-2),Bcl-2 related X protein(Bax)protein expression.MTT assay was used to detect cell viability.Flow cytometry was used to detect apoptosis.Luciferase reporter assay was used to detect the targeting relationship between miR-647 and NLRC5.Results:Low expression of miR-647 and high expression of NLRC5 in endometrial cancer tissues(P<0.05).Overexpression of miR-647 or inhibition of NLRC5 expression,cell viability was significantly reduces,the rate of apoptosis was significantly increases,the expressions of CyclinD1,Bcl-2 were significantly reduced,and the expressions of p21 and Bax were significantly increased(P<0.05).miR-647 targets NLRC5,overexpression of NLRC5 reverses the effect of miR-647 overexpression on the proliferation and apoptosis of endometrial cancer Ishikawa cells.Conclusion:Overexpression of miR-647 may inhibit the proliferation of endometrial cancer cells and promote apoptosis through targeted down-regulation of NLRC5.
作者
饶珺
陈金玲
冯元元
常璐
赵玉杰
RAO Jun;CHEN Jinling;FENG Yuanyuan;CHANG Lu;ZHAO Yujie(Department of Gynecology,Xinyang Central Hospital,Henan Xinyang 464000,China;Department of Gynecology,Xuchang Central Hospital,Henan Xuchang 461000,China)
出处
《现代肿瘤医学》
CAS
北大核心
2022年第17期3096-3101,共6页
Journal of Modern Oncology