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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 被引量:5

Identification of actin cytoskeleton and extracellular matrix down-regulation in human bladder cancer by suppression subtractive hybridization
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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。 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.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2002年第6期503-505,共3页 Chinese Journal of Experimental Surgery
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 Bladder neoplasms Actin Extracellular matrix Gene
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  • 1杨靖轩.高效率感受态细胞的制备.见:卢圣栋,主编.现代分子生物学实验技术.第2版.北京:高等教育出版社,1999.293.
  • 2Matsumoto K,Takayama N,Ohnishi J,et al.Tumour invasion and metastasis are promoted in mice deficient in tenascin-X.Genes Cells,2001,6:1101-1111.
  • 3Rao JY.Targeting actin remodeling profiles for the detection and management of urothelial cancers-a perspective for bladder cancer research.Front Biosci,2002,7:1-8.

同被引文献47

  • 1王玉荣,王敏,孙凤娟.子宫肌瘤组织中胰岛素样生长因子-Ⅰ和ⅡmRNA表达及意义[J].中国实用妇科与产科杂志,2005,21(12):753-754. 被引量:3
  • 2王玮,许伟,丁淑玉,周宝森.以人群为基础子宫肌瘤危险因素病例对照研究[J].中华肿瘤防治杂志,2007,14(11):821-823. 被引量:24
  • 3Lees-Miller J P, Heeley D H, Smillie L B. An abundant and novel protein of 22 kDa is widely distributed in smooth museles[J]. Biochem J,1987,244(3) :705 -709.
  • 4Camoretti-Mercado B, Forsythe S M. Expression and cytogenetic localization of the human SM22 gene (transgelin) [J]. Genomics,1998,49(3) :452-457.
  • 5Shields J M, Rogers Graham K, Der C J. Loss of transgelin in breast and colon tumors and in RIE-1 cells by Ras deregulation of gene expression through Raf -independent pathways[J]. J Biol Chem, 2002,277(12) :9790-9799.
  • 6Yeo M, Kim D K, Park H J, et aI. Loss of transgelin in repeated bouts of ulcerative colitis induced colon carcinogenesis[J]. Proteomics, 2006,6(4):1158- 1165.
  • 7Weitz J,Koch M,Debus J,et al.Colorectal cancer[J].Lancet,2005,365:153.
  • 8Feng YY,Walsh CA.The many faces of flamin:a versatile molecular scaffold for cell motility and signaling[J].Nat Cell Biol,2004,6(11):1034.
  • 9Nakamur a F,Osborn TM,Hartemink CA,et al.Structure basis of filamin A functions[J].J Cell Biol,2007,179(5):1011.
  • 10Otti,Fischer E G,Miyagiy,et al.A role for tissue factor in cell adhesion and migration mediated by interaction with actin-binding protein 280[J].J CellBiol,1998,140(5):1241.

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