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Runx3对人肝癌HepG2细胞增殖、凋亡及侵袭的影响 被引量:3

Effect of Runx3 on the proliferation,apoptosis and invasion of HepG2 cells
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摘要 目的探讨siRNA干扰Runx3对人肝癌Hep G2细胞增殖、凋亡和侵袭能力的影响。方法以人肝癌Hep G2细胞为研究对象,构建Runx3-siRNA,转染入细胞。将细胞分为对照组、脂质体组、NC-siRNA组和Runx3-siRNA组。用RT-PCR法检测Runx3 mRNA表达,用Western blot检测Runx3蛋白表达。用MTT法、流式细胞法和Transwell小室法观察Runx3对Hep G2细胞增殖、凋亡和侵袭的影响。结果 Runx3-siRNA可抑制Hep G2细胞的增殖(P<0.05);Runx3-siRNA可促进Hep G2细胞凋亡(P<0.05);Runx3-siRNA可抑制Hep G2细胞的侵袭(P<0.05)。结论Runx3基因在肝癌的发生发展中发挥一定的促进作用,有可能成为肝癌治疗的新靶点。 Objective To explore the effect of siRNA targeting Runx3 on proliferation,apoptosis,and invasive ability of Hep G2 cells. Methods The Runx3-siRNA was transfected into Hep G2 cells. Hep G2 cells were divided into four groups: control group,liposomes group,NC-siRNA group and Runx3-siRNA group. The expression levels of Runx3 mRNA and Runx3 protein were examined by RT-PCR and Western blotting. MTT assay,flow cytometry and Transwell chamber were used to determine the effect of Runx3 on Hep G2 cells proliferation,apoptosis and migration. Results MTT assay showed that the proliferation of Hep G2 cells was obviously inhibited by Runx3-siRNA. Flow cytometry demonstrated that the apoptosis of Hep G2 cells was promoted by Runx3-siRNA. The invasion of Hep G2 cells was also significantly inhibited by Runx3-siRNA according to Transwell chamber assay. Conclusions Silence Runx3 could effectively inhibit cell proliferation and migration,and promote apoptosis in Hep G2 cells. Our study shows that Runx3 gene plays an important role on the occurrence and development in hepatocellular carcinoma. Runx3 is a potential target in the treatment of hepatocellular carcinoma.
出处 《基础医学与临床》 CSCD 2015年第3期383-386,共4页 Basic and Clinical Medicine
关键词 RUNT相关转录因子3 HEPG2细胞 增殖 凋亡 侵袭 runt-related transcription factor3(Runx3) HepG2 cells proliferation apoptosis invasion
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  • 1杨克红,许冰莹,葛树星,闫俊岭,卢珊珊,吴兰鸥.Real time RT-PCR定量检测BDNF mRNA表达水平方法的建立[J].昆明医学院学报,2007,28(2):34-38. 被引量:1
  • 2Laurent Puig P, Legoix P, Bluteau O, et al. Genetic alterations associated with hepatocellular carcinomas define distinct pathways of hepoatocarcinogenesis. Gastroenterology, 2001, 120: 1763-1773. 被引量:1
  • 3Bergsland EK. Molecular mechanisms underlying the development of hepatocellular carcinoma. Semin Oncol, 2001, 28: 521-531. 被引量:2
  • 4Li QL, Ito K, Sakaura C, et al. Causal relationship between the loss of RUNX3 expression and gastric cancer. Cell, 2002, 109:113-124. 被引量:2
  • 5Fang W, Piao Z, Simon D, et al. Mapping of a minimal deleted region in human hepatocellular carcinoma to l p36.13-p36.33 and mutational analysis of the RIZ (PRDM2) gene localized to the region.Genes Chromosomes Cancer, 2000, 28: 269-275. 被引量:2
  • 6Zaidi SK, Sullivon AJ, Wijnen AJV, et al. Integration of Runx and Smad regulatory signals at transcriptionally active subnuclear sites.Proc Natl Acad Sci, 2002, 99: 8048-8053. 被引量:2
  • 7Song BC, Chung YH, Kim JA, et al. Transforming growth factorbetal as a useful serologic marker of small hepatocellular carcinoma.Cancer, 2002, 94: 175-180. 被引量:2
  • 8Matuzaki K, Date M, Furukawa F, et al. Regulatory mechanisms for transforming growth factor beta as an autocrine inhibitor in human hepatocellalar carcinoma: implications for roles of smads in its growth.Hepatology, 2000, 32: 218-227. 被引量:2
  • 9肖文华,刘为纹,吕有勇,高崇峰.肝细胞癌多种抑癌基因失活机理的研究[J].第三军医大学学报,1997,19(4):324-328. 被引量:10
  • 10肖文华,刘为纹,吕有勇,高崇峰.Rb基因在肝细胞癌中的多种失活机制[J].中华肝脏病杂志,1997,5(3):142-144. 被引量:4

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