Wilms' tumour 1 can suppress hTERT gene expression and telomerase activity in clear cell renal cell carcinoma via multiple pathways

被引:31
作者
Sitaram, R. T. [2 ]
Degerman, S. [2 ]
Ljungberg, B. [3 ]
Andersson, E. [2 ]
Oji, Y. [4 ]
Sugiyama, H. [5 ]
Roos, G. [2 ]
Li, A. [1 ]
机构
[1] Umea Univ, Dept Med Biosci & Clin Chem, SE-90185 Umea, Sweden
[2] Umea Univ, Dept Med Biosci & Pathol, SE-90185 Umea, Sweden
[3] Umea Univ, Dept Perioperat Sci Urol & Androl, SE-90185 Umea, Sweden
[4] Osaka Univ, Grad Sch Med, Dept Canc Stem Cell Biol, Osaka, Japan
[5] Osaka Univ, Grad Sch Med, Dept Funct Diagnost Sci, Osaka, Japan
关键词
renal cell carcinoma; WT1; hTERT; telomerase activity and pathways; REVERSE-TRANSCRIPTASE PROMOTER; REGULATORY FACTOR-I; CANCER-CELLS; C-MYC; WT1; PROTEIN; ACTIVATION; IDENTIFICATION; OVEREXPRESSION; BINDING; DIFFERENTIATION;
D O I
10.1038/sj.bjc.6605878
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Wilms' tumour 1 (WT1) gene was discovered as a tumour suppressor gene. Later findings have suggested that WT1 also can be oncogenic. This complexity is partly explained by the fact that WT1 has a number of target genes. METHOD: WT1 and its target gene human telomerase reverse transcriptase (hTERT) were analysed in clear cell renal cell carcinoma (ccRCC). In vitro experiments were performed to examine the functional link between WT1 and hTERT by overexpression of WT1 isoforms in the ccRCC cell line, TK-10. RESULTS: WT1 demonstrated lower RNA expression in ccRCC compared with renal cortical tissue, whereas hTERT was increased, showing a negative correlation between WT1 and hTERT (P = 0.005). These findings were experimentally confirmed in vitro. The WT1 generated effect on hTERT promoter activity seemed complex, as several negative regulators of hTERT transcription, such as SMAD3, JUN (AP-1) and ETS1, were activated by WT1 overexpression. Downregulation of potential positive hTERT regulators, such as cMyc, AP-2 alpha, AP-2 gamma, IRF1, NFX1 and GM-CSF, were also observed. Chromatin immunoprecipitation analysis verified WT1 binding to the hTERT, cMyc and SMAD3 promoters. CONCLUSION: The collected data strongly indicate multiple pathways for hTERT regulation by WT1 in ccRCC. British Journal of Cancer (2010) 103, 1255-1262. doi:10.1038/sj.bjc.6605878 www.bjcancer.com Published online 14 September 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1255 / 1262
页数:8
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