| Literature DB >> 24589892 |
Chiara Fiorentini1, Serena Bodei1, Francesca Bedussi1, Martina Fragni1, Sara Anna Bonini1, Claudio Simeone2, Danilo Zani2, Alfredo Berruti3, Cristina Missale1, Maurizio Memo1, PierFranco Spano1, Sandra Sigala4.
Abstract
Non-metastatic glycoprotein melanoma protein B (GPNMB), also known as osteoactivin (OA) is expressed in a wide array of tumors and represents an emerging target for drug development. In this study, we investigated the role of GPNMB/OA in the progression of human metastatic DU145 and PC3 prostate cancer cells. GPNMB/OA contribution in PCa malignant phenotype has been analyzed by small interfering RNA-induced GPNMB/OA silencing. We found that following GPNMB/OA silencing the migration capability of both DU145 and PC3 cells, evaluated by using in vitro invasivity assay, as well as the metalloproteinases MMP-2 and MMP-9 activity were equally strongly inhibited. By contrast knocking down GPNMB/OA weakly attenuated cell proliferation rate of DU145, an effect that paralleled with an increase number of apoptotic cells. However, PC3 cell growth seems to be not affected by GPNMB/OA. Together, these data reveal that GPNMB/OA acts as a critical molecular mediator promoting the acquisition of the more aggressive, pro-metastatic phenotype distinctive of human DU145 and PC3 cell lines.Entities:
Keywords: Apoptosis; GPNMB/osteoactivin; Invasivity; Metalloproteinases; Prostate cancer
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Year: 2014 PMID: 24589892 DOI: 10.1016/j.yexcr.2014.02.025
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905