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Snail在卵巢癌细胞侵袭转移潜能方面研究
引用本文:夏曦,蒋学峰,纪腾,徐洪斌.Snail在卵巢癌细胞侵袭转移潜能方面研究[J].医学分子生物学杂志,2013,10(1):21-25.
作者姓名:夏曦  蒋学峰  纪腾  徐洪斌
作者单位:夏曦 (广东医学院附属深圳市南山区人民医院妇产科,广东省深圳市,518052华中科技大学同济医学院附属同济医院肿瘤生物医学中心,武汉市,430030); 蒋学峰 (广东医学院附属深圳市南山区人民医院妇产科,广东省深圳市,518052华中科技大学同济医学院附属同济医院肿瘤生物医学中心,武汉市,430030); 纪腾 (华中科技大学同济医学院附属同济医院肿瘤生物医学中心,武汉市,430030);徐洪斌 (华中科技大学同济医学院附属同济医院肿瘤生物医学中心,武汉市,430030;暨南大学附属深圳市人民医院妇产科,广东省深圳市,518020);
基金项目:广东省自然科学基金(项目编号:S2011040006012)广东省医学科研基金(项目编号:B2011295)深圳市科技计划(项目编号:20110422597,201002006)深圳市南山区科技计划(项目编号:2010028)
摘    要:目的研究Snail与卵巢癌侵袭转移问的关系,并探讨其分子机制。方法分别构建正义全长Snail真核表达载体和小分子干扰RNA,分别转染卵巢癌细胞系A2780、C13*。采用Western印迹方法分析相关蛋白表达,Transwell试验检测细胞侵袭转移能力。结果①成功构建Snail正义全长真核表达载体,并合成Snail小分子RNA干扰片段;②在转染PEGFPCI/Snail的卵巢癌细胞株A2780、C13*中E-eadhefin表达明显下调,Snail和Vimentin则表达上调;而在转染Snail/SiRNA的卵巢癌细胞株A2780、C13‘中E—cadherin表达明显上调,Snail和Vimentin则表达下调;③Snail过表达可显著促进卵巢癌细胞株A2780、C13*的侵袭转移潜能;封闭Snail表达水平可一定水平抑制卵巢癌细胞株A2780、C13*的侵袭转移潜能。结论snail可通过促进卵巢癌上皮细胞间质化转变(epithelial—mesenchymaltransition,EMT)而提高其侵袭转移能力;封闭Snail表达可一定程度逆转卵巢癌上皮细胞间质化转变(EMT)而抑制其侵袭转移能力。

关 键 词:转录因子Snail  卵巢癌侵袭转移  上皮间质变(EMT)  e-cadherin  vimentin

Role of Snail in the Invasion and Migration of Ovarian Carcinoma Cells
XIA Xi,JIANG Xuefeng,JI Teng,XU Hongbin.Role of Snail in the Invasion and Migration of Ovarian Carcinoma Cells[J].Journal of Medical Molecular Biology,2013,10(1):21-25.
Authors:XIA Xi  JIANG Xuefeng  JI Teng  XU Hongbin
Institution:1 Department of Gynecology & Obstetrics, Nanshan People' s Hospital, Guangdong Medical College, Shenzhen, 518052, China 2 Cancer Biology Research Center, Tongji Hospital, Tong/i Medical School, Huazhong University of Science and Technology, Wuhan , 430030, China 3 Department of Gynecology and Obstetrics, People's Hospital of Shenzhen, Jinan University, Shenz- hen, 518020, China)
Abstract:Objective To examine the relationship between Snail and the invasion and migra- tion of ovarian carcinoma cells and the underlying molecular mechanism. Methods The eukaryotic expression vector carrying full-length sense Snail gene and the Snail-targeting small molecule RNA interference fragment were constructed and transfected into A2780 and C13 * cells (two ovarian car- cinoma cell lines) respectively. Western blotting was used to detect the expression of Snail, E-cad- herin and Vimentin. The invasive and migratory ability of cells was examined by transwell as- say. Results The Snail over-expressing plasmid PEGFPC1/Snail and the small molecule RNA in- terference fragment Snail/siRNA were successfully constructed. After the PEGFPC1/Snail transfec- tion, the expression level of E-cadherin was significantly decreased and that of Snail and Vimentin substantially increased in A2780 and C13 * cells. Transfection with Snail/SiRNA resulted in an in-crease in the expression of E-cadherin and a decrease in the expression of Snail and Vimentin in A2780 and C13 * cells. Snail overexpression contributed to the invasion and migration of A2780 and C13 * cells and Snail silencing inhibited such abilities of the cells. Conclusion Snail may enhance the potential of invasion and migration of ovarian carcinoma cells by inducing epithelial-mesenchymal transition (EMT) . Snail silencing may inhibit the cell invasion and migration by reversing the change of EMT.
Keywords:Snail  invasion  migration  ovarian carcinoma  epithelial-mesenchymal transi-tion (EMT)  E-cadherin  vimentin
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