Src: marker or actor of prostate cancer aggressiveness

A key question for urologic practitioners is whether an apparently organ-confined prostate cancer is actually aggressive or not. The dilemma is to specifically identify among all prostate tumors the very aggressive high-grade cancers that will become life-threatening by developing extra-prostatic in...

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Main Authors: Virginie eVlaeminck-Guillem, Germain eGILLET, Ruth eRIMOKH
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-08-01
Series:Frontiers in Oncology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00222/full
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author Virginie eVlaeminck-Guillem
Virginie eVlaeminck-Guillem
Germain eGILLET
Ruth eRIMOKH
author_facet Virginie eVlaeminck-Guillem
Virginie eVlaeminck-Guillem
Germain eGILLET
Ruth eRIMOKH
author_sort Virginie eVlaeminck-Guillem
collection DOAJ
description A key question for urologic practitioners is whether an apparently organ-confined prostate cancer is actually aggressive or not. The dilemma is to specifically identify among all prostate tumors the very aggressive high-grade cancers that will become life-threatening by developing extra-prostatic invasion and metastatic potential and the indolent cancers that will never modify a patient’s life expectancy. A choice must be made between several therapeutic options to achieve the optimal personalized management of the disease that causes as little harm as possible to patients. Reliable clinical, biological or pathological markers that would enable distinctions to be made between aggressive and indolen prostate cancers in routine practice at the time of initial diagnosis are still lacking. The molecular mechanisms that explain why a prostate cancer is aggressive or not are also poorly understood. Among the potential markers and/or actors in prostate cancer aggressiveness, Src and other members of the Src kinase family, are valuable candidates. Activation of Src-dependent intracellular pathways is frequently observed in prostate cancer. Indeed, Src is at the cross-roads of several pathways (including androgen receptor, TGFbeta, Bcl-2, Akt/PTEN or MAPK and ERK …), and is now known to influence some of the cellular and tissular events that accompany tumor progression: cell proliferation, cell motility, invasion, epithelial-to-mesenchymal transition, resistance to apoptosis, angiogenesis, neuroendocrine differentiation, and metastatic spread. Recent work even suggests that Src could also play a part in prostate cancer initiation in coordination with the androgen receptor. The aim of this review is to gather data that explores the links between the Src kinase family and prostate cancer progression and aggressiveness.
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spelling doaj.art-2a5f969bbec546f2a0e69d48f2d6e9c62022-12-21T19:01:51ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2014-08-01410.3389/fonc.2014.00222105025Src: marker or actor of prostate cancer aggressivenessVirginie eVlaeminck-Guillem0Virginie eVlaeminck-Guillem1Germain eGILLET2Ruth eRIMOKH3Cancer Research Centre of LyonHospices Civils of LyonCancer Research Centre of LyonCancer Research Centre of LyonA key question for urologic practitioners is whether an apparently organ-confined prostate cancer is actually aggressive or not. The dilemma is to specifically identify among all prostate tumors the very aggressive high-grade cancers that will become life-threatening by developing extra-prostatic invasion and metastatic potential and the indolent cancers that will never modify a patient’s life expectancy. A choice must be made between several therapeutic options to achieve the optimal personalized management of the disease that causes as little harm as possible to patients. Reliable clinical, biological or pathological markers that would enable distinctions to be made between aggressive and indolen prostate cancers in routine practice at the time of initial diagnosis are still lacking. The molecular mechanisms that explain why a prostate cancer is aggressive or not are also poorly understood. Among the potential markers and/or actors in prostate cancer aggressiveness, Src and other members of the Src kinase family, are valuable candidates. Activation of Src-dependent intracellular pathways is frequently observed in prostate cancer. Indeed, Src is at the cross-roads of several pathways (including androgen receptor, TGFbeta, Bcl-2, Akt/PTEN or MAPK and ERK …), and is now known to influence some of the cellular and tissular events that accompany tumor progression: cell proliferation, cell motility, invasion, epithelial-to-mesenchymal transition, resistance to apoptosis, angiogenesis, neuroendocrine differentiation, and metastatic spread. Recent work even suggests that Src could also play a part in prostate cancer initiation in coordination with the androgen receptor. The aim of this review is to gather data that explores the links between the Src kinase family and prostate cancer progression and aggressiveness.http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00222/fullprostate cancerbiomarkerprognosisaggressivenessepithelial-to-mesenchymal transitionc-src
spellingShingle Virginie eVlaeminck-Guillem
Virginie eVlaeminck-Guillem
Germain eGILLET
Ruth eRIMOKH
Src: marker or actor of prostate cancer aggressiveness
Frontiers in Oncology
prostate cancer
biomarker
prognosis
aggressiveness
epithelial-to-mesenchymal transition
c-src
title Src: marker or actor of prostate cancer aggressiveness
title_full Src: marker or actor of prostate cancer aggressiveness
title_fullStr Src: marker or actor of prostate cancer aggressiveness
title_full_unstemmed Src: marker or actor of prostate cancer aggressiveness
title_short Src: marker or actor of prostate cancer aggressiveness
title_sort src marker or actor of prostate cancer aggressiveness
topic prostate cancer
biomarker
prognosis
aggressiveness
epithelial-to-mesenchymal transition
c-src
url http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00222/full
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