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Association between HPV infection and prostate cancer in a Mexican population

The aim of this study was to evaluate the association between prostate cancer (PCa) and Human papillomavirus (HPV) infection in the Mexican population. We studied 356 paraffin-embedded tissues from unrelated Mexican men with PCa or benign prostatic hyperplasia (BPH), with the latter serving as contr...

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Autores principales: Medel-Flores, Olivia, Valenzuela-Rodríguez, Vania Alejandra, Ocadiz-Delgado, Rodolfo, Castro-Muñoz, Leonardo Josué, Hernández-Leyva, Sandra, Lara-Hernández, Gabriel, Silva-Escobedo, Jesús-Gabriel, Vidal, Patricio Gariglio, Sánchez-Monroy, Virginia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415601/
https://www.ncbi.nlm.nih.gov/pubmed/30508006
http://dx.doi.org/10.1590/1678-4685-GMB-2017-0331
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author Medel-Flores, Olivia
Valenzuela-Rodríguez, Vania Alejandra
Ocadiz-Delgado, Rodolfo
Castro-Muñoz, Leonardo Josué
Hernández-Leyva, Sandra
Lara-Hernández, Gabriel
Silva-Escobedo, Jesús-Gabriel
Vidal, Patricio Gariglio
Sánchez-Monroy, Virginia
author_facet Medel-Flores, Olivia
Valenzuela-Rodríguez, Vania Alejandra
Ocadiz-Delgado, Rodolfo
Castro-Muñoz, Leonardo Josué
Hernández-Leyva, Sandra
Lara-Hernández, Gabriel
Silva-Escobedo, Jesús-Gabriel
Vidal, Patricio Gariglio
Sánchez-Monroy, Virginia
author_sort Medel-Flores, Olivia
collection PubMed
description The aim of this study was to evaluate the association between prostate cancer (PCa) and Human papillomavirus (HPV) infection in the Mexican population. We studied 356 paraffin-embedded tissues from unrelated Mexican men with PCa or benign prostatic hyperplasia (BPH), with the latter serving as control. HPV detection was performed by polymerase chain reaction (PCR) using universal primers, and viral genotypes were detected using sequencing or multiplex PCR. Light microscopy analyses enabled the identification of koilocytes in samples subsequently analyzed for HPV detection by in situ PCR and for p16-INK4A expression by immunohistochemistry. The results showed that high risk- (HR) HPVs were detected in 37/189 (19.6%) PCa specimens compared to 16/167 (9.6%) of BHP specimens (odds ratio 2.3; 95% CI= 1.2 to 4.3; p=0.01). These data suggest HR-HPV may play a role in PCa. HPV 52 and 58 were the most frequent genotypes (33 and 17%, respectively) detected in the population studied. Koilocytes were detected in all in situ PCR-HPV-positive samples, representing a pathognomonic feature of infection, and we observed the overexpression of p16-INK4A in HPV-positive samples compared to HPV-negative samples, indirectly suggesting the presence of HR-HPV E7 oncoprotein. These results suggest that HPV infection plays an important role in prostate cancer development.
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spelling pubmed-64156012019-03-21 Association between HPV infection and prostate cancer in a Mexican population Medel-Flores, Olivia Valenzuela-Rodríguez, Vania Alejandra Ocadiz-Delgado, Rodolfo Castro-Muñoz, Leonardo Josué Hernández-Leyva, Sandra Lara-Hernández, Gabriel Silva-Escobedo, Jesús-Gabriel Vidal, Patricio Gariglio Sánchez-Monroy, Virginia Genet Mol Biol Human and Medical Genetics The aim of this study was to evaluate the association between prostate cancer (PCa) and Human papillomavirus (HPV) infection in the Mexican population. We studied 356 paraffin-embedded tissues from unrelated Mexican men with PCa or benign prostatic hyperplasia (BPH), with the latter serving as control. HPV detection was performed by polymerase chain reaction (PCR) using universal primers, and viral genotypes were detected using sequencing or multiplex PCR. Light microscopy analyses enabled the identification of koilocytes in samples subsequently analyzed for HPV detection by in situ PCR and for p16-INK4A expression by immunohistochemistry. The results showed that high risk- (HR) HPVs were detected in 37/189 (19.6%) PCa specimens compared to 16/167 (9.6%) of BHP specimens (odds ratio 2.3; 95% CI= 1.2 to 4.3; p=0.01). These data suggest HR-HPV may play a role in PCa. HPV 52 and 58 were the most frequent genotypes (33 and 17%, respectively) detected in the population studied. Koilocytes were detected in all in situ PCR-HPV-positive samples, representing a pathognomonic feature of infection, and we observed the overexpression of p16-INK4A in HPV-positive samples compared to HPV-negative samples, indirectly suggesting the presence of HR-HPV E7 oncoprotein. These results suggest that HPV infection plays an important role in prostate cancer development. Sociedade Brasileira de Genética 2018-11-29 2018 /pmc/articles/PMC6415601/ /pubmed/30508006 http://dx.doi.org/10.1590/1678-4685-GMB-2017-0331 Text en Copyright © 2018, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
spellingShingle Human and Medical Genetics
Medel-Flores, Olivia
Valenzuela-Rodríguez, Vania Alejandra
Ocadiz-Delgado, Rodolfo
Castro-Muñoz, Leonardo Josué
Hernández-Leyva, Sandra
Lara-Hernández, Gabriel
Silva-Escobedo, Jesús-Gabriel
Vidal, Patricio Gariglio
Sánchez-Monroy, Virginia
Association between HPV infection and prostate cancer in a Mexican population
title Association between HPV infection and prostate cancer in a Mexican population
title_full Association between HPV infection and prostate cancer in a Mexican population
title_fullStr Association between HPV infection and prostate cancer in a Mexican population
title_full_unstemmed Association between HPV infection and prostate cancer in a Mexican population
title_short Association between HPV infection and prostate cancer in a Mexican population
title_sort association between hpv infection and prostate cancer in a mexican population
topic Human and Medical Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415601/
https://www.ncbi.nlm.nih.gov/pubmed/30508006
http://dx.doi.org/10.1590/1678-4685-GMB-2017-0331
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