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The Role of Androgen Receptor Mutations in Prostate Cancer Progression

Prostate tumour growth is almost always dependent upon the androgen receptor pathway and hence therapies aimed at blocking this signalling axis are useful tools in the management of this disease. Unfortunately such therapies invariably fail; and the tumour progresses to an “androgen-independent” sta...

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Detalles Bibliográficos
Autores principales: Brooke, G.N, Bevan, C.L
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699836/
https://www.ncbi.nlm.nih.gov/pubmed/19721807
http://dx.doi.org/10.2174/138920209787581307
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author Brooke, G.N
Bevan, C.L
author_facet Brooke, G.N
Bevan, C.L
author_sort Brooke, G.N
collection PubMed
description Prostate tumour growth is almost always dependent upon the androgen receptor pathway and hence therapies aimed at blocking this signalling axis are useful tools in the management of this disease. Unfortunately such therapies invariably fail; and the tumour progresses to an “androgen-independent” stage. In such cases androgen receptor expression is almost always maintained and much evidence exists to suggest that it may still be driving growth. One mechanism by which the receptor is thought to remain active is mutation. This review summarises the present data on androgen receptor mutations in prostate cancer, and how such substitutions offer a growth advantage by affecting cofactor interactions or by reducing ligand specificity. Such alterations appear to have a subsequent effect upon gene expression suggesting that tumours may “behave” differently dependent upon the ligand promoting growth and if a mutation is present.
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spelling pubmed-26998362009-09-01 The Role of Androgen Receptor Mutations in Prostate Cancer Progression Brooke, G.N Bevan, C.L Curr Genomics Article Prostate tumour growth is almost always dependent upon the androgen receptor pathway and hence therapies aimed at blocking this signalling axis are useful tools in the management of this disease. Unfortunately such therapies invariably fail; and the tumour progresses to an “androgen-independent” stage. In such cases androgen receptor expression is almost always maintained and much evidence exists to suggest that it may still be driving growth. One mechanism by which the receptor is thought to remain active is mutation. This review summarises the present data on androgen receptor mutations in prostate cancer, and how such substitutions offer a growth advantage by affecting cofactor interactions or by reducing ligand specificity. Such alterations appear to have a subsequent effect upon gene expression suggesting that tumours may “behave” differently dependent upon the ligand promoting growth and if a mutation is present. Bentham Science Publishers Ltd. 2009-03 /pmc/articles/PMC2699836/ /pubmed/19721807 http://dx.doi.org/10.2174/138920209787581307 Text en ©2009 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Brooke, G.N
Bevan, C.L
The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title_full The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title_fullStr The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title_full_unstemmed The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title_short The Role of Androgen Receptor Mutations in Prostate Cancer Progression
title_sort role of androgen receptor mutations in prostate cancer progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699836/
https://www.ncbi.nlm.nih.gov/pubmed/19721807
http://dx.doi.org/10.2174/138920209787581307
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