NON-GENOMIC ANDROGEN ACTION REGULATES PROLIFERATIVE/MIGRATORY SIGNALLING IN STROMAL CELLS.

Prostate cancer is the major cause of cancer-related death among the male population of Western society, and androgen deprivation therapy represents the first line in prostate cancer treatment. However, although androgen receptor expression is maintained throughout the various stages of prostate can...

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Bibliographic Details
Main Authors: Marzia eDi Donato, Pia eGiovannelli, Gustavo eCernera, Annalisa eDi Santi, Irene eMarino, Antonio eBilancio, Giovanni eGalasso, Ferdinando eAuricchio, Antimo eMigliaccio, Gabriella eCastoria
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-01-01
Series:Frontiers in Endocrinology
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2014.00225/full
Description
Summary:Prostate cancer is the major cause of cancer-related death among the male population of Western society, and androgen deprivation therapy represents the first line in prostate cancer treatment. However, although androgen receptor expression is maintained throughout the various stages of prostate cancer, androgen deprivation therapy frequently fails. Clinical studies have demonstrated that different androgen/androgen receptor signalling pathways operate in target tissues. Androgen receptor stimulates growth and transformation of target cells, but under certain conditions slows down their proliferation. In this review we discuss the role of androgen receptor in controlling different functions of mesenchymal and transformed mesenchymal cells. Findings here presented support the role of androgen receptor in suppressing proliferation and stimulating migration of stromal cells, with implications for current approaches to cancer therapy.
ISSN:1664-2392