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抑制乙肝病毒X蛋白表达对肝癌细胞上皮一间质转化和凋亡的影响 被引量:1

Effect of Inhibiting of HBx expression on epithelial-mesenchymai transition and apoptosis of liver cancercells
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摘要 目的探讨乙肝病毒x蛋白(HBx)对肝癌细胞转移能力的影响及其机制。方法采用siRNA干扰技术抑制MHCC97H细胞的HBx表达。通过Transwell小室和裸鼠肺转移模型实验比较HBx抑制前后MHCC97H细胞转移能力的变化。应用Western blotting技术检测肝癌细胞上皮间质转化(EMT)和凋亡相关基因的表达变化。结果将Hgx-siRNA导入MHCC97H细胞可以抑制HBx的表达及其转移能力,可下调EMT相关分子Twist和N—cadherin的表达,并上调E—cad—herin表达而抑制EMT,同时还可通过Twist—P53途径诱发细胞的凋亡。结论抑制HBx表达可以通过改变上皮一间质转化和诱发凋亡而减弱高侵袭肝癌细胞MHCC7H的转移能力。 Objective To investigate the effects and possible mechanism of action of inhibiting hepatitis B virus X protein (HBx) expression on liver cancer metastasis. Methods The suppression of HBx expression in MHCC97H cells was performed by siRNA interference technique, and the effects of HBx suppression on the metastasis of MHCC97H cells were detected by Matrigel invasion assays and in a lung-metastasis mouse model. The expression levels of related epithelial-mesenchymal transi- tion (EMT) and apoptosis proteins were examined by Western blotting. Results Introduction of HBx-siRNA into MHCC97H cells inhibited the expression of HBx and the ability to metastasize, downregulated the expression of Twist and N-cadherin, and upregulated E-cadherin expression. These changes resulted in inhibiting EMT of MHCC97H cells. Meanwhile, apoptosis involved in the Twist- P53 pathway was also found. Concluslbns Inhibiting expression of HBx can decrease the metastatic a- bility of MHCC97H ceils by changing EMT and inducing apoptosis.
出处 《中华肝胆外科杂志》 CAS CSCD 北大核心 2011年第7期566-570,共5页 Chinese Journal of Hepatobiliary Surgery
基金 厦门市科学技术局科技计划项目资助(3502220084021)
关键词 乙肝病毒X蛋白 肝癌细胞 上皮一间质转化 凋亡 Hepatitis B virus X protein Liver cancer cell Epithelial-mesenchymal transition Apoptosis
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  • 1李常海,陈孝平,徐宗全,李高鹏,关剑.Twist基因在肝细胞肝癌中的表达及意义[J].中华外科杂志,2006,44(19):1353-1356. 被引量:4
  • 2Mitsuteru N, Takumi O, Toru A, et al. Clinical features of hepatocellular carcinoma with extrahepatic metastases. J Gastroenterology Hepatol,2005,20 : 1781-1787.
  • 3Brigitte B, Ana MV, Natacha E. Induction and regulation of epithelial-mesenchymal transitions. Biochemical Pharmacology, :2000,60 : 1091-1099.
  • 4Thiery JP. Epithelial-mesenchymal transition in tumor progression. Nature Rev Cancer,2002,2:442-454.
  • 5Giannelli G, Bergamini C, Fransvea E, et al. Laminin-5 With Transforming Growth Factor-β1 Induces Epithelial to Mesenchymal Transition in Hepatocellular Carcinoma. Gastroenterology, 2005, 129 : 1375-1383.
  • 6Christofori G,Semb H. The role of the cell-adhesion molecule E- cadherin as a tumour-suppressor gene. Trends Biochem Sci, 1999, 24 : 73 -76.
  • 7Hu L, Lau SH, Tzang CH, et at. Association of Vimentin overexpression and hepatocellular carcinoma metastasis. Oncogene, 2004,23 : 298 -302.
  • 8[1]Clements WM,Wang J,Sarnaik A,Kim OJ,MacDonald J,Fenoglio-Preiser C,Groden J,Lowy AM.beta-Catenin mutation is a frequent cause of Wnt pathway activation in gastric cancer.Cancer Res 2002; 62:3503-3506
  • 9[2]Offerhaus GJ,Giardiello FM,Krush AJ,Booker SV,Tersmette AC,Kelley NC,Hamilton SR.The risk of upper gastrointestinal cancer in familial adenomatous polyposis.Gastroenterology 1992; 102:1980-1982
  • 10[3]Nakatsuru S,Yanagisawa A,Ichii S,Tahara E,Kato Y,Nakamura Y,Horii A.Somatic mutation of the APC gene in gastric cancer:frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma.Hum Mol Genet 1992; 1:559-563

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