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抑制性消减杂交分析肌动蛋白细胞骨架和细胞外基质基因在膀胱癌中的表达下调
引用本文:刘晓琼,秦杨,付捷,吕任奇,杨林,王瑾雯,龙綮新,王珣章. 抑制性消减杂交分析肌动蛋白细胞骨架和细胞外基质基因在膀胱癌中的表达下调[J]. 中华实验外科杂志, 2002, 19(6): 503-505
作者姓名:刘晓琼  秦杨  付捷  吕任奇  杨林  王瑾雯  龙綮新  王珣章
作者单位:1. 510275,广州,中山大学生物防治国家重点实验室生物医药中心
2. 云南省肿瘤医院泌尿外科中心实验室
摘    要:目的:分析膀胱移行细胞癌的差异表达基因,探讨肿瘤行为的分子生物学基础及筛选有效的肿瘤标记。方法:应用抑制性消减杂交(SSH)方法构建在正常膀胱组织和膀胱癌组织中差异表达序列的消减文库,用差异筛选技术分离差异表达基因。结果:从消减文库中共获得了9个在正常膀胱组织中高表达、在膀胱癌组织中表达下调的基因,分别属于细胞外基质成分和肌动蛋白细胞骨架体系。结论:细胞外基质和肌动蛋白细胞骨架体系中相关基因的表达下调可能反映了肿瘤细胞在细胞粘附、细胞间相互作用、迁移及运动等诸多过程中的异常,可能与癌细胞的侵袭和转移密切相关,对发展成为膀胱癌的分子标记物具有潜在价值;gelsolin、tuopomyosin等抑癌基因在膀胱癌形成过程中可能起了重要作用。

关 键 词:抑制性消减杂交分析 肌动蛋白 细胞骨架 细胞外基质基因 膀胱癌 基因表达
修稿时间:2002-06-09

Identification of actin cytoskeleton and extracellular matrix down-regulation in human bladder cancer by suppression subtractive hybridization
LIU Xiaoqiong ,QIN Yang,FU Jie,et al.. Identification of actin cytoskeleton and extracellular matrix down-regulation in human bladder cancer by suppression subtractive hybridization[J]. Chinese Journal of Experimental Surgery, 2002, 19(6): 503-505
Authors:LIU Xiaoqiong   QIN Yang  FU Jie  et al.
Affiliation:LIU Xiaoqiong *,QIN Yang,FU Jie,et al. *Biopharmaceutical Center,State Key Laboratory for Biological Control,College of Life Sciences,Zhongshan University,Guangzhou 510275,China
Abstract:Objective To identify the genes differentially expressed in human urinary transitional cell carcinoma.Methods Suppression subtractive hybridization was performed using primary tumor tissues as driver and normal urinary epithelia as tester.Down regulated genes in tumor cells were identified by differential screening method.Results 9 genes were identified in bladder tumor tissues showing decreased mRNA levels.They either belong to the extracellular matrix family.Conclusion Alterations of extracellular matrix components and actin cytoskeleton may be general effector events during the development of bladder cancer and may provide potential tumor biomarkers.Gelsolin and tropomyosin may play tumor suppressor roles in the tumorigenesis of bladder cancer.
Keywords:Bladder neoplasms  Actin  Extracellular matrix  Gene
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