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Death receptor 5 expression is inversely correlated with prostate cancer progression

Prostate carcinoma (PCa) is one of the most common cancers in men. Prostate-specific antigen (PSA) has been widely used to predict the outcome of PCa and screening with PSA has resulted in a decline in mortality. However, PSA is not an optimal prognostic tool as its sensitivity may be too low to red...

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Autores principales: HERNANDEZ-CUETO, ANGELES, HERNANDEZ-CUETO, DANIEL, ANTONIO-ANDRES, GABRIELA, MENDOZA-MARIN, MARISELA, JIMENEZ-GUTIERREZ, CARLOS, SANDOVAL-MEJIA, ANA LILIA, MORA-CAMPOS, ROSARIO, GONZALEZ-BONILLA, CESAR, VEGA, MARIO I., BONAVIDA, BENJAMIN, HUERTA-YEPEZ, SARA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214341/
https://www.ncbi.nlm.nih.gov/pubmed/25174820
http://dx.doi.org/10.3892/mmr.2014.2504
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author HERNANDEZ-CUETO, ANGELES
HERNANDEZ-CUETO, DANIEL
ANTONIO-ANDRES, GABRIELA
MENDOZA-MARIN, MARISELA
JIMENEZ-GUTIERREZ, CARLOS
SANDOVAL-MEJIA, ANA LILIA
MORA-CAMPOS, ROSARIO
GONZALEZ-BONILLA, CESAR
VEGA, MARIO I.
BONAVIDA, BENJAMIN
HUERTA-YEPEZ, SARA
author_facet HERNANDEZ-CUETO, ANGELES
HERNANDEZ-CUETO, DANIEL
ANTONIO-ANDRES, GABRIELA
MENDOZA-MARIN, MARISELA
JIMENEZ-GUTIERREZ, CARLOS
SANDOVAL-MEJIA, ANA LILIA
MORA-CAMPOS, ROSARIO
GONZALEZ-BONILLA, CESAR
VEGA, MARIO I.
BONAVIDA, BENJAMIN
HUERTA-YEPEZ, SARA
author_sort HERNANDEZ-CUETO, ANGELES
collection PubMed
description Prostate carcinoma (PCa) is one of the most common cancers in men. Prostate-specific antigen (PSA) has been widely used to predict the outcome of PCa and screening with PSA has resulted in a decline in mortality. However, PSA is not an optimal prognostic tool as its sensitivity may be too low to reduce morbidity and mortality. Consequently, there is a demand for additional robust biomarkers for prostate cancer. Death receptor 5 (DR5) has been implicated in the prognosis of several cancers and it has been previously shown that it is negatively regulated by Yin Yang 1 (YY1) in prostate cancer cell lines. The present study investigated the clinical significance of DR5 expression in a prostate cancer patient cohort and its correlation with YY1 expression. Immunohistochemical analysis of protein expression distribution was performed using tissue microarray constructs from 54 primary PCa and 39 prostatic intraepithelial neoplasia (PIN) specimens. DR5 expression was dramatically reduced as a function of higher tumor grade. By contrast, YY1 expression was elevated in PCa tumors as compared with that in PIN, and was increased with higher tumor grade. DR5 had an inverse correlation with YY1 expression. Bioinformatic analyses corroborated these data. The present findings suggested that DR5 and YY1 expression levels may serve as progression biomarkers for prostate cancer.
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spelling pubmed-42143412014-10-30 Death receptor 5 expression is inversely correlated with prostate cancer progression HERNANDEZ-CUETO, ANGELES HERNANDEZ-CUETO, DANIEL ANTONIO-ANDRES, GABRIELA MENDOZA-MARIN, MARISELA JIMENEZ-GUTIERREZ, CARLOS SANDOVAL-MEJIA, ANA LILIA MORA-CAMPOS, ROSARIO GONZALEZ-BONILLA, CESAR VEGA, MARIO I. BONAVIDA, BENJAMIN HUERTA-YEPEZ, SARA Mol Med Rep Articles Prostate carcinoma (PCa) is one of the most common cancers in men. Prostate-specific antigen (PSA) has been widely used to predict the outcome of PCa and screening with PSA has resulted in a decline in mortality. However, PSA is not an optimal prognostic tool as its sensitivity may be too low to reduce morbidity and mortality. Consequently, there is a demand for additional robust biomarkers for prostate cancer. Death receptor 5 (DR5) has been implicated in the prognosis of several cancers and it has been previously shown that it is negatively regulated by Yin Yang 1 (YY1) in prostate cancer cell lines. The present study investigated the clinical significance of DR5 expression in a prostate cancer patient cohort and its correlation with YY1 expression. Immunohistochemical analysis of protein expression distribution was performed using tissue microarray constructs from 54 primary PCa and 39 prostatic intraepithelial neoplasia (PIN) specimens. DR5 expression was dramatically reduced as a function of higher tumor grade. By contrast, YY1 expression was elevated in PCa tumors as compared with that in PIN, and was increased with higher tumor grade. DR5 had an inverse correlation with YY1 expression. Bioinformatic analyses corroborated these data. The present findings suggested that DR5 and YY1 expression levels may serve as progression biomarkers for prostate cancer. D.A. Spandidos 2014-11 2014-08-21 /pmc/articles/PMC4214341/ /pubmed/25174820 http://dx.doi.org/10.3892/mmr.2014.2504 Text en Copyright © 2014, 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
HERNANDEZ-CUETO, ANGELES
HERNANDEZ-CUETO, DANIEL
ANTONIO-ANDRES, GABRIELA
MENDOZA-MARIN, MARISELA
JIMENEZ-GUTIERREZ, CARLOS
SANDOVAL-MEJIA, ANA LILIA
MORA-CAMPOS, ROSARIO
GONZALEZ-BONILLA, CESAR
VEGA, MARIO I.
BONAVIDA, BENJAMIN
HUERTA-YEPEZ, SARA
Death receptor 5 expression is inversely correlated with prostate cancer progression
title Death receptor 5 expression is inversely correlated with prostate cancer progression
title_full Death receptor 5 expression is inversely correlated with prostate cancer progression
title_fullStr Death receptor 5 expression is inversely correlated with prostate cancer progression
title_full_unstemmed Death receptor 5 expression is inversely correlated with prostate cancer progression
title_short Death receptor 5 expression is inversely correlated with prostate cancer progression
title_sort death receptor 5 expression is inversely correlated with prostate cancer progression
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214341/
https://www.ncbi.nlm.nih.gov/pubmed/25174820
http://dx.doi.org/10.3892/mmr.2014.2504
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