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The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients

Levels of enzymes that determine testosterone catabolism such as CYP3A4 have been associated with prostate cancer (PCa) risk. Although some studies have related CYP3A4*1B allele, a gene polymorphism that modifies CYP3A4 expression level, with PCa risk, others have failed, suggesting that additional...

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Autores principales: Reyes-Hernández, Octavio D., Vega, Libia, Jiménez-Ríos, Miguel A., Martínez-Cervera, Pedro F., Lugo-García, Juan A., Hernández-Cadena, Leticia, Ostrosky-Wegman, Patricia, Orozco, Lorena, Elizondo, Guillermo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055777/
https://www.ncbi.nlm.nih.gov/pubmed/24924803
http://dx.doi.org/10.1371/journal.pone.0099974
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author Reyes-Hernández, Octavio D.
Vega, Libia
Jiménez-Ríos, Miguel A.
Martínez-Cervera, Pedro F.
Lugo-García, Juan A.
Hernández-Cadena, Leticia
Ostrosky-Wegman, Patricia
Orozco, Lorena
Elizondo, Guillermo
author_facet Reyes-Hernández, Octavio D.
Vega, Libia
Jiménez-Ríos, Miguel A.
Martínez-Cervera, Pedro F.
Lugo-García, Juan A.
Hernández-Cadena, Leticia
Ostrosky-Wegman, Patricia
Orozco, Lorena
Elizondo, Guillermo
author_sort Reyes-Hernández, Octavio D.
collection PubMed
description Levels of enzymes that determine testosterone catabolism such as CYP3A4 have been associated with prostate cancer (PCa) risk. Although some studies have related CYP3A4*1B allele, a gene polymorphism that modifies CYP3A4 expression level, with PCa risk, others have failed, suggesting that additional genetic variants may be involved. Expression of CYP3A4 is largely due to the activation of Pregnane X Receptor (PXR). Particularly, rs2472677 and rs7643645 PXR polymorphisms modify CYP3A4 expression levels. To evaluate whether PXR-HNF3β/T (rs2472677), PXR-HNF4/G (rs7643645), and CYP3A4*1B (rs2740574) polymorphisms are associated with PCa a case control-study was performed. The multiple testing analysis showed that the PXR-HNF4/G polymorphism was associated with higher levels of prostate-specific antigen (PSA) in patients with PCa (OR = 3.99, p = 0.03). This association was stronger in patients diagnosed at the age of 65 years or older (OR = 10.8, p = 0.006). Although the CYP3A4*1B/*1B genotype was overrepresented in PCa patients, no differences were observed in the frequency of this and PXR-HNF3β/T alleles between controls and cases. Moreover, no significant association was found between these polymorphisms and PSA, Gleason grade, or tumor lymph node metastasis.
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spelling pubmed-40557772014-06-18 The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients Reyes-Hernández, Octavio D. Vega, Libia Jiménez-Ríos, Miguel A. Martínez-Cervera, Pedro F. Lugo-García, Juan A. Hernández-Cadena, Leticia Ostrosky-Wegman, Patricia Orozco, Lorena Elizondo, Guillermo PLoS One Research Article Levels of enzymes that determine testosterone catabolism such as CYP3A4 have been associated with prostate cancer (PCa) risk. Although some studies have related CYP3A4*1B allele, a gene polymorphism that modifies CYP3A4 expression level, with PCa risk, others have failed, suggesting that additional genetic variants may be involved. Expression of CYP3A4 is largely due to the activation of Pregnane X Receptor (PXR). Particularly, rs2472677 and rs7643645 PXR polymorphisms modify CYP3A4 expression levels. To evaluate whether PXR-HNF3β/T (rs2472677), PXR-HNF4/G (rs7643645), and CYP3A4*1B (rs2740574) polymorphisms are associated with PCa a case control-study was performed. The multiple testing analysis showed that the PXR-HNF4/G polymorphism was associated with higher levels of prostate-specific antigen (PSA) in patients with PCa (OR = 3.99, p = 0.03). This association was stronger in patients diagnosed at the age of 65 years or older (OR = 10.8, p = 0.006). Although the CYP3A4*1B/*1B genotype was overrepresented in PCa patients, no differences were observed in the frequency of this and PXR-HNF3β/T alleles between controls and cases. Moreover, no significant association was found between these polymorphisms and PSA, Gleason grade, or tumor lymph node metastasis. Public Library of Science 2014-06-12 /pmc/articles/PMC4055777/ /pubmed/24924803 http://dx.doi.org/10.1371/journal.pone.0099974 Text en © 2014 Reyes-Hernandez et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Reyes-Hernández, Octavio D.
Vega, Libia
Jiménez-Ríos, Miguel A.
Martínez-Cervera, Pedro F.
Lugo-García, Juan A.
Hernández-Cadena, Leticia
Ostrosky-Wegman, Patricia
Orozco, Lorena
Elizondo, Guillermo
The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title_full The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title_fullStr The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title_full_unstemmed The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title_short The PXR rs7643645 Polymorphism Is Associated with the Risk of Higher Prostate-Specific Antigen Levels in Prostate Cancer Patients
title_sort pxr rs7643645 polymorphism is associated with the risk of higher prostate-specific antigen levels in prostate cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055777/
https://www.ncbi.nlm.nih.gov/pubmed/24924803
http://dx.doi.org/10.1371/journal.pone.0099974
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