Novel WWP2 ubiquitin ligase isoforms as potential prognostic markers and molecular targets in cancer

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• 作者：Surinder M. Soond ; Paul G. Smith ; Lloyd Wahl ; Tracey E. Swingler ; Ian M. Clark ; Andrew M. Hemmings ; Andrew Chantry
• 关键词：TGF尾 ; Smads ; Ubiquitin ligase ; Transcription ; Cancer ; EMT
• 刊名：Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease
• 出版年：December, 2013
• 年：2013
• 卷：1832
• 期：12
• 页码：2127-2135
• 全文大小：1277 K

文摘

The WWP2 E3 ubiquitin ligase has previously been shown to regulate TGF尾/Smad signalling activity linked to epithelial-mesenchymal transition (EMT). Whilst inhibitory I-Smad7 was found to be the preferred substrate for full-length WWP2-FL and a WWP2-C isoform, WWP2-FL also formed a stable complex with an N-terminal WWP2 isoform (WWP2-N) in the absence of TGF尾, and rapidly stimulated activating Smad2/3 turnover. Here, using stable knockdown experiments we show that specific depletion of individual WWP2 isoforms impacts differentially on Smad protein levels, and in WWP2-N knockdown cells we unexpectedly find spontaneous expression of the EMT marker vimentin. Re-introduction of WWP2-N into WWP2-N knockout cells also repressed TGF尾-induced vimentin expression. In support of the unique role for WWP2-N in regulating TGF尾/Smad functional activity, we then show that a novel V717M-WWP2 mutant in the MZ7-mel melanoma cell line forms a stable complex with the WWP2-N isoform and promotes EMT by stabilizing Smad3 protein levels. Finally, we report the first analysis of WWP2 expression in cancer cDNA panel arrays using WWP2 isoform-specific probes and identify unique patterns of WWP2 isoform abundance associated with early/advanced disease stages. WWP2-N is significantly downregulated in stage IIIC melanoma and up-regulated in stage II/III prostate cancer, and we also find isolated examples of WWP2-FL and WWP2-C overexpression in early-stage breast cancer. Together, these data suggest that individual WWP2 isoforms, and particularly WWP2-N, could play central roles in tumourigenesis linked to aberrant TGF尾-dependent signalling function, and also have potential as both prognostic markers and molecular therapeutic targets.