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

Sitaram, Raviprakash T, 1974- (författare)
Umeå universitet,Patologi
Degerman, Sofie (författare)
Umeå universitet,Patologi
Ljungberg, Börje (författare)
Umeå universitet,Urologi och andrologi
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Andersson, Emma (författare)
Umeå universitet,Patologi
Oji, Y (författare)
Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Osaka, Japan
Sugiyama, H (författare)
Department of Functional Diagnostic Science, Osaka University Graduate School of Medicine, Osaka, Japan
Roos, Göran (författare)
Umeå universitet,Patologi
Li, Ai-Hong (författare)
Umeå universitet,Klinisk kemi
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 (creator_code:org_t)
2010-09-14
2010
Engelska.
Ingår i: British Journal of Cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 103:8, s. 1255-1262
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • 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-2α, AP-2γ, 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.

Nyckelord

renal cell carcinoma; WT1; hTERT; telomerase activity and pathways

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