The transcripts of SFRP1, CEP63 and EIF4G2 genes are frequently downregulated in transitional cell carcinomas of the bladder

被引:21
作者
Buim, ME
Soares, FA
Sarkis, AS
Nagai, MA
机构
[1] Univ Sao Paulo, Fac Med, Dept Radiol, Disciplina Oncol, BR-01246903 Sao Paulo, Brazil
[2] FMUSP, HC, Fundacao Antonio Prudente, Sao Paulo, Brazil
[3] FMUSP, HC, Dept Urol, Div Clin Urol, Sao Paulo, Brazil
关键词
bladder cancer; differential gene expression; SFRP1; EIF4G2; CEP63;
D O I
10.1159/000090984
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The aim of the present study was to identify differentially expressed genes that might be associated with the phenotype of superficial and invasive bladder cancer. Methods: Differential display reverse transcriptase PCR ( DDRT-PCR) was used to compare the expression pattern between normal bladder tissue and 4 groups of transitional cell carcinomas of the bladder regarding clinical stage and grade. Results: We were able to identify 72 different transcripts, of which 57 (79%) showed homology to known genes, 12 (17%) to hypothetical proteins and 3 (4%) to human expressed sequence tags. Among the differentially expressed genes, SFRP1, CEP63 and EIF4G2 were further validated by quantitative RTPCR in a series of 50 transitional cell carcinomas. Overall, the transcripts of these three genes were shown to be downregulated in the bladder tumors analyzed. In accordance with the DDRT-PCR results, the SFRP1 transcripts were shown to be downregulated in 90% (45/50) of the bladder tumors as compared with the normal bladder tissue. Although EIF4G2 and CEP63 transcripts exhibited three different expression patterns, downregulation was found in about 50% of the cases analyzed. In addition, downregulation of both CEP63 and EIF4G2 gene transcription was associated with invasive tumors. Conclusion: The use of DDRT-PCR analysis to compare expression patterns among different subgroups of bladder tumors allowed us to identify a significant number of genes implicated in different cellular pathways that, when up- or downregulated, might play a role in the tumorigenic process of the bladder. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:445 / 454
页数:10
相关论文
共 53 条
[1]   Proteomic characterization of the human centrosome by protein correlation profiling [J].
Andersen, JS ;
Wilkinson, CJ ;
Mayor, T ;
Mortensen, P ;
Nigg, EA ;
Mann, M .
NATURE, 2003, 426 (6966) :570-574
[2]  
Bane BL, 1996, SEMIN ONCOL, V23, P546
[3]   IRESdb:: the internal ribosome entry site database [J].
Bonnal, S ;
Boutonnet, C ;
Prado-Lourenço, L ;
Vagner, S .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :427-428
[4]   Centrosome composition and microtubule anchoring mechanisms [J].
Bornens, M .
CURRENT OPINION IN CELL BIOLOGY, 2002, 14 (01) :25-34
[5]   Managing the centrosome numbers game: from chaos to stability in cancer cell division [J].
Brinkley, BR .
TRENDS IN CELL BIOLOGY, 2001, 11 (01) :18-21
[6]   The Wnt antagonist sFRP1 in colorectal tumorigenesis [J].
Caldwell, GM ;
Jones, C ;
Gensberg, K ;
Jan, S ;
Hardy, RG ;
Byrd, P ;
Chughtai, S ;
Wallis, Y ;
Matthews, GM ;
Morton, DG .
CANCER RESEARCH, 2004, 64 (03) :883-888
[7]   Translational control of gene expression and disease [J].
Calkhoven, CF ;
Müller, C ;
Leutz, A .
TRENDS IN MOLECULAR MEDICINE, 2002, 8 (12) :577-583
[8]   AZU-1:: A candidate breast tumor suppressor and biomarker for tumor progression [J].
Chen, HM ;
Schmeichel, KL ;
Mian, IS ;
Lelièvre, S ;
Petersen, OW ;
Bissell, MJ .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (04) :1357-1367
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]  
Crew JP, 2000, BRIT J CANCER, V82, P161