Downregulation and growth inhibitory effect of epithelial-type Kruppel-like transcription factor KLF4, but not KLF5, in bladder cancer

被引:159
作者
Ohnishi, S
Ohnami, S
Laub, F
Aoki, K
Suzuki, K
Kanai, Y
Haga, K
Asaka, M
Ramirez, F
Yoshida, T [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Genet, Tokyo 1040045, Japan
[2] Hokkaido Univ, Sch Med, Dept Internal Med 3, Sapporo, Hokkaido 0608638, Japan
[3] Mt Sinai Sch Med, Dept Biochem & Mol Biol, Brookdale Ctr, New York, NY 10029 USA
[4] Natl Canc Ctr, Res Inst, Div Pathol, Tokyo 1040045, Japan
[5] Hokkaido Univ, Sch Med, Div Urol, Sapporo, Hokkaido 0608638, Japan
关键词
Kruppel-like factor; KLF4; KLF5; bladder cancer; tumor suppressor;
D O I
10.1016/S0006-291X(03)01356-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kruppel-like factors (KLFs) are key transcriptional regulators of cell differentiation and proliferation. Among the KLF family, the expression of KLF4 (GKLF) and KLF5 (IKLF) is highly restricted in the epithelial cells of several organs such as the gut and skin, and it has been reported that these epithelial-type KLF genes may be involved in colon carcinogenesis. Recently we found that Klf4 and Klf5 genes were significantly expressed in the developmental bladder epithelium of mice as well. Therefore, in this report we studied the involvement of the KLF4 and KLF5 genes in bladder carcinogenesis. First, we analyzed the expression of KLF4 and KLF5 in a variety of human bladder cancer cell lines and surgical specimens by RNA blot and in situ hybridization analyses. Both genes were highly expressed in the normal bladder epithelium, whereas KLF4, but not KLF5, was frequently downregulated in bladder cancer cell lines and cancer tissues. We then transduced the KLF4 and KLF5 genes into the bladder cancer cell lines using adenoviral vectors to examine the biological activities of the genes on those cells. The transduction of KLF4, but not KLF5, suppressed cell growth and induced apoptosis. Our study suggests that inactivation of KLF4 is one of the frequent steps towards bladder carcinogenesis. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:251 / 256
页数:6
相关论文
共 26 条
  • [1] Efficient generation of recombinant adenoviral vectors by Cre-lox recombination in vitro
    Aoki, K
    Barker, C
    Danthinne, X
    Imperiale, MJ
    Nabel, GJ
    [J]. MOLECULAR MEDICINE, 1999, 5 (04) : 224 - 231
  • [2] Kruppel-like factors: Three fingers in many pies
    Bieker, JJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (37) : 34355 - 34358
  • [3] Kruppel-like factor 4 (Gut-enriched Kruppel-like factor) inhibits cell proliferation by blocking G1/S progression of the cell cycle
    Chen, XM
    Johns, DC
    Geiman, DE
    Marban, E
    Dang, DT
    Hamlin, G
    Sun, RG
    Yang, VW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (32) : 30423 - 30428
  • [4] Up-regulation of gut-enriched kruppel-like factor by interferon-γ in human colon carcinoma cells
    Chen, ZY
    Shie, JL
    Tseng, CC
    [J]. FEBS LETTERS, 2000, 477 (1-2) : 67 - 72
  • [5] Gut-enriched Kruppel-like factor represses ornithine decarboxylase gene expression and functions as checkpoint regulator in colonic cancer cells
    Chen, ZY
    Shie, JL
    Tseng, CC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (48) : 46831 - 46839
  • [6] A gene encoding an intestinal-enriched member of the Kruppel-like factor family expressed in intestinal epithelial cells
    Conkright, MD
    Wani, MA
    Anderson, KP
    Lingrel, JB
    [J]. NUCLEIC ACIDS RESEARCH, 1999, 27 (05) : 1263 - 1270
  • [7] Expression of the gut-enriched Kruppel-like factor (Kruppel-like factor 4) gene in the human colon cancer cell line RKO is dependent on CDX2
    Dang, DT
    Mahatan, CS
    Dang, LH
    Agboola, IA
    Yang, VW
    [J]. ONCOGENE, 2001, 20 (35) : 4884 - 4890
  • [8] Decreased expression of the gut-enriched Kruppel-like factor gene in intestinal adenomas of multiple intestinal neoplasia mice and in colonic adenomas of familial adenomatous polyposis patients
    Dang, DT
    Bachman, KE
    Mahatan, CS
    Dang, LH
    Giardiello, FM
    Yang, VW
    [J]. FEBS LETTERS, 2000, 476 (03) : 203 - 207
  • [9] Foster KW, 1999, CELL GROWTH DIFFER, V10, P423
  • [10] Foster KW, 2000, CANCER RES, V60, P6488