首页|MiR-92a-3p靶向KLF4促进肝细胞癌恶性进程

MiR-92a-3p靶向KLF4促进肝细胞癌恶性进程

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目的:探究微小RNA-92a-3p(miR-92a-3p)对肝细胞癌(HCC)的影响及其分子机制。方法:qRT-PCR检测人肝细胞癌细胞系SMMC-7721、Bel-7402、HepG2、Hep3B 和人正常肝细胞系HL-7702 中miR-92a-3p和Krüppel样因子4(KLF4)的表达。将SMMC-7721、Bel-7402 细胞分组为Inhibi-tor NC组、miR-92a-3p Inhibitor组、mimic NC组、miR-92a-3p mimic组、mimic NC+oe-NC组、mimic NC +oe-KLF4 组、miR-92a-3p mimic +oe-NC组、miR-92a-3p mimic +oe-KLF4 组。qRT-PCR检测细胞中miR-92a-3p和KLF4 的mRNA表达水平。Western blot检测KLF4 蛋白表达水平。MTT增殖实验检测细胞活力。划痕愈合、Transwell 侵袭实验分别检测细胞迁移能力和侵袭能力。通过 TargetScan 分析miR-92a-3p与 KLF4 的靶向关系,并通过双荧光素酶实验验证。结果:相比于正常细胞,miR-92a-3p在HCC细胞中高表达,KLF4 在HCC细胞中低表达(P<0。05)。与正常表达组相比,下调 miR-92a-3p显著抑制了SMMC-7721 和Bel-7402 细胞的增殖、迁移、侵袭能力(P<0。05)。双荧光素酶实验验证了miR-92a-3p与KLF4 存在靶向结合位点。过表达KLF4 能够阻碍HCC 细胞的增殖、迁移和侵袭,抑制过表达miR-92a-3p对HCC细胞生长的促进作用,差异有统计学意义(P<0。05)。结论:miR-92a-3p能够通过靶向下调KLF4 来促进HCC细胞的增殖、迁移、侵袭。
MiR-92a-3p Targeting KLF4 to Promote Malignant Progression of Hepatocellular Carcinoma
Objective:To investigate the effect of microRNA-92a-3p(miR-92a-3p)on hepatocellu-lar carcinoma(HCC)and its molecular mechanism.Methods:qRT-PCR was used to detect the expression of miR-92a-3p and Krüppel-like factor 4(KLF4)in human HCC cell lines SMMC-7721,Bel-7402,HepG2,Hep3B,and human normal liver cell line HL-7702.SMMC-7721 and Bel-7402 cells were divided into eight groups:Inhibitor NC group,miR-92a-3p Inhibitor group,mimic NC group,miR-92a-3p mimic group,mimic NC+oe-NC group,mimic NC+oe-KLF4 group,miR-92a-3p mimic +oe-NC group,and miR-92a-3p mimic +oe-KLF4 group.qRT-PCR was used to detect the mRNA expression levels of miR-92a-3p and KLF4 in cells.Western blot was used to detect the protein expression levels of KLF4.MTT proliferation assay was used to detect cell viability.Scratch healing and Transwell invasion assays were used to detect cell migration and invasion abilities,respectively.TargetScan was used to analyze the targeting relationship be-tween miR-92a-3p and KLF4,and the results were verified by dual luciferase assay.Results:Compared with normal cells,miR-92a-3p was highly expressed in HCC cells,and KLF4 was lowly expressed in HCC cells(P<0.05).Compared with the normal expression group,down-regulation of miR-92a-3p significantly in-hibited the proliferation,migration,and invasion abilities of SMMC-7721 and Bel-7402 cells(P<0.05).The dual luciferase assay verified the existence of a targeting binding site between miR-92a-3p and KLF4.Overexpression of KLF4 was able to inhibit the proliferation,migration,and invasion of HCC cells,and inhib-it the promoting effect of overexpressed miR-92a-3p on HCC cell growth,with statistical significance(P<0.05).Conclusion:miR-92a-3p can promote proliferation,migration,and invasion of HCC cells by targeting down-regulation of KLF4.

HCCmiR-92a-3pKLF4ProliferationMigrateAttack

蔡青山、郑建兴、申月玲、吴东洋、李树栋、刘立友、刘东

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河北省唐山市中心医院肝胆外科, 河北 唐山 063000

河北省迁安市人民医院耳鼻喉科, 河北 迁安 064499

肝细胞癌 miR-92a-3p KLF4 增殖 迁移 侵袭

2022年度河北省医学科学研究课题计划

20221840

2024

河北医学
河北省医学会

河北医学

CSTPCD
影响因子:1.915
ISSN:1006-6233
年,卷(期):2024.30(2)
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