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Transforming growth factor-β promotes aggressiveness and invasion of clear cell renal cell carcinoma.
Umeå University, Faculty of Medicine, Department of Surgical and Perioperative Sciences. Medical Biosciences. (Urology)
2016 (English)In: OncoTarget, ISSN 1949-2553, E-ISSN 1949-2553Article in journal (Refereed) Epub ahead of print
Abstract [en]

The molecular mechanisms whereby transforming growth factor-β (TGF-β) promotes clear cell renal cell carcinoma (ccRCC) progression is elusive. The cell membrane bound TGF-β type I receptor (ALK5), was recently found to undergo proteolytic cleavage in aggressive prostate cancer cells, resulting in liberation and subsequent nuclear translocation of its intracellular domain (ICD), suggesting that ALK5-ICD might be a useful cancer biomarker. Herein, the possible correlation between ALK5 full length (ALK5-FL) and ALK5-ICD protein, phosphorylated Smad2/3 (pSmad2/3), and expression of TGF-β target gene PAI-1, was investigated in a clinical ccRCC material, in relation to tumor grade, stage, size and cancer specific survival. Expression of ALK5-FL, ALK5-ICD, pSmad2/3 and PAI-1 protein levels were significantly higher in higher stage and associated with adverse survival. ALK5-ICD, pSmad2/3 and PAI-1 correlated with higher grade, and ALK5-FL, pSmad2/3 and PAI-1 protein levels were significantly correlated with larger tumor size. Moreover, the functional role of the TGF-β - ALK5-ICD pathway were investigated in two ccRCC cell lines by treatment with ADAM/MMP2 inhibitor TAPI-2, which prevented TGF-β-induced ALK5-ICD generation, nuclear translocation, as well as cell invasion. The present study demonstrated that canonical TGF-β Smad2/3 pathway and generation of ALK5-ICD correlates with poor survival and invasion of ccRCC in vitro.

Place, publisher, year, edition, pages
2016.
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Medical and Health Sciences
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URN: urn:nbn:se:umu:diva-120254DOI: 10.18632/oncotarget.9177PubMedID: 27166254OAI: oai:DiVA.org:umu-120254DiVA: diva2:927569
Available from: 2016-05-12 Created: 2016-05-12 Last updated: 2016-05-12

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