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Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo

BACKGROUND: Membrane androgen receptors (mAR) have been implicated in the regulation of cell growth, motility and apoptosis in prostate and breast cancer. Here we analyzed mAR expression and function in colon cancer. RESULTS: Using fluorescent mAR ligands we showed specific membrane staining in colo...

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Autores principales: Gu, Shuchen, Papadopoulou, Natalia, Gehring, Eva-Maria, Nasir, Omaima, Dimas, Konstantinos, Bhavsar, Shefalee K, Föller, Michael, Alevizopoulos, Konstantinos, Lang, Florian, Stournaras, Christos
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794856/
https://www.ncbi.nlm.nih.gov/pubmed/19948074
http://dx.doi.org/10.1186/1476-4598-8-114
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author Gu, Shuchen
Papadopoulou, Natalia
Gehring, Eva-Maria
Nasir, Omaima
Dimas, Konstantinos
Bhavsar, Shefalee K
Föller, Michael
Alevizopoulos, Konstantinos
Lang, Florian
Stournaras, Christos
author_facet Gu, Shuchen
Papadopoulou, Natalia
Gehring, Eva-Maria
Nasir, Omaima
Dimas, Konstantinos
Bhavsar, Shefalee K
Föller, Michael
Alevizopoulos, Konstantinos
Lang, Florian
Stournaras, Christos
author_sort Gu, Shuchen
collection PubMed
description BACKGROUND: Membrane androgen receptors (mAR) have been implicated in the regulation of cell growth, motility and apoptosis in prostate and breast cancer. Here we analyzed mAR expression and function in colon cancer. RESULTS: Using fluorescent mAR ligands we showed specific membrane staining in colon cell lines and mouse xenograft tumor tissues, while membrane staining was undetectable in healthy mouse colon tissues and non-transformed intestinal cells. Saturation/displacement assays revealed time- and concentration-dependent specific binding for testosterone with a K(D )of 2.9 nM. Stimulation of colon mAR by testosterone albumin conjugates induced rapid cytoskeleton reorganization and apoptotic responses, even in the presence of anti-androgens. The actin cytoskeleton drug cytochalasin B effectively inhibited the pro-apoptotic responses and caspase-3 activation. Interestingly, in vivo studies revealed that mAR activation resulted in a 65% reduction of tumor incidence in chemically induced Balb/c mice colon tumors. CONCLUSION: Our results demonstrate for the first time that functional mARs are predominantly expressed in colon tumors and that their activation results in induction of anti-tumor responses in vitro and extensive reduction of tumor incidence in vivo.
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spelling pubmed-27948562009-12-17 Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo Gu, Shuchen Papadopoulou, Natalia Gehring, Eva-Maria Nasir, Omaima Dimas, Konstantinos Bhavsar, Shefalee K Föller, Michael Alevizopoulos, Konstantinos Lang, Florian Stournaras, Christos Mol Cancer Research BACKGROUND: Membrane androgen receptors (mAR) have been implicated in the regulation of cell growth, motility and apoptosis in prostate and breast cancer. Here we analyzed mAR expression and function in colon cancer. RESULTS: Using fluorescent mAR ligands we showed specific membrane staining in colon cell lines and mouse xenograft tumor tissues, while membrane staining was undetectable in healthy mouse colon tissues and non-transformed intestinal cells. Saturation/displacement assays revealed time- and concentration-dependent specific binding for testosterone with a K(D )of 2.9 nM. Stimulation of colon mAR by testosterone albumin conjugates induced rapid cytoskeleton reorganization and apoptotic responses, even in the presence of anti-androgens. The actin cytoskeleton drug cytochalasin B effectively inhibited the pro-apoptotic responses and caspase-3 activation. Interestingly, in vivo studies revealed that mAR activation resulted in a 65% reduction of tumor incidence in chemically induced Balb/c mice colon tumors. CONCLUSION: Our results demonstrate for the first time that functional mARs are predominantly expressed in colon tumors and that their activation results in induction of anti-tumor responses in vitro and extensive reduction of tumor incidence in vivo. BioMed Central 2009-12-01 /pmc/articles/PMC2794856/ /pubmed/19948074 http://dx.doi.org/10.1186/1476-4598-8-114 Text en Copyright ©2009 Gu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Gu, Shuchen
Papadopoulou, Natalia
Gehring, Eva-Maria
Nasir, Omaima
Dimas, Konstantinos
Bhavsar, Shefalee K
Föller, Michael
Alevizopoulos, Konstantinos
Lang, Florian
Stournaras, Christos
Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title_full Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title_fullStr Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title_full_unstemmed Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title_short Functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
title_sort functional membrane androgen receptors in colon tumors trigger pro-apoptotic responses in vitro and reduce drastically tumor incidence in vivo
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794856/
https://www.ncbi.nlm.nih.gov/pubmed/19948074
http://dx.doi.org/10.1186/1476-4598-8-114
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