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From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells

Elucidating the role of androgen deprivation in the transition from androgen-dependence to independence may enable the development of more specific therapeutic strategies against prostate cancer. Our previous in vitro model was employed to further assess the effects of continuous androgen-deprivatio...

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Detalles Bibliográficos
Autores principales: LIU, TIANCHENG, MENDES, DESIREE E., BERKMAN, CLIFFORD E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 201
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829778/
https://www.ncbi.nlm.nih.gov/pubmed/23877345
http://dx.doi.org/ 10.3892/ijo.2013.2020
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author LIU, TIANCHENG
MENDES, DESIREE E.
BERKMAN, CLIFFORD E.
author_facet LIU, TIANCHENG
MENDES, DESIREE E.
BERKMAN, CLIFFORD E.
author_sort LIU, TIANCHENG
collection PubMed
description Elucidating the role of androgen deprivation in the transition from androgen-dependence to independence may enable the development of more specific therapeutic strategies against prostate cancer. Our previous in vitro model was employed to further assess the effects of continuous androgen-deprivation on prostate cancer cells (LNCaP) with respect to both androgen receptor (AR) and c-Met expression. The results indicated that long-term androgen deprivation resulted in a signaling pathway switch from AR to c-Met in androgen-sensitive cells, which was confirmed by immunofluorescence imaging and western blot analysis. This signaling pathway switch may be predictive of a more aggressive disease state following androgen deprivation therapy.
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spelling pubmed-38297782013-11-18 From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells LIU, TIANCHENG MENDES, DESIREE E. BERKMAN, CLIFFORD E. Int J Oncol Articles Elucidating the role of androgen deprivation in the transition from androgen-dependence to independence may enable the development of more specific therapeutic strategies against prostate cancer. Our previous in vitro model was employed to further assess the effects of continuous androgen-deprivation on prostate cancer cells (LNCaP) with respect to both androgen receptor (AR) and c-Met expression. The results indicated that long-term androgen deprivation resulted in a signaling pathway switch from AR to c-Met in androgen-sensitive cells, which was confirmed by immunofluorescence imaging and western blot analysis. This signaling pathway switch may be predictive of a more aggressive disease state following androgen deprivation therapy. D.A. Spandidos 2013 -07- 18 /pmc/articles/PMC3829778/ /pubmed/23877345 http://dx.doi.org/ 10.3892/ijo.2013.2020 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LIU, TIANCHENG
MENDES, DESIREE E.
BERKMAN, CLIFFORD E.
From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title_full From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title_fullStr From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title_full_unstemmed From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title_short From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells
title_sort from ar to c-met: androgen deprivation leads to a signaling pathway switch in prostate cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829778/
https://www.ncbi.nlm.nih.gov/pubmed/23877345
http://dx.doi.org/ 10.3892/ijo.2013.2020
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