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Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males

Sexually transmitted infections and its contribution to prostate cancer (PC) development have been relevant in different populations. MSMB gene polymorphism (rs10993994) has exhibited an association both with PC as well as the susceptibility to sexually transmitted infections. Hitherto, these condit...

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Autores principales: Trujillo-Cáceres, Silvia Juliana, Torres-Sánchez, Luisa, Burguete-García, Ana I., Orbe Orihuela, Yaneth Citlalli, Vázquez-Salas, Ruth Argelia, Álvarez-Topete, Esmeralda, Gómez, Rocío
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366823/
https://www.ncbi.nlm.nih.gov/pubmed/30774776
http://dx.doi.org/10.18632/oncotarget.26592
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author Trujillo-Cáceres, Silvia Juliana
Torres-Sánchez, Luisa
Burguete-García, Ana I.
Orbe Orihuela, Yaneth Citlalli
Vázquez-Salas, Ruth Argelia
Álvarez-Topete, Esmeralda
Gómez, Rocío
author_facet Trujillo-Cáceres, Silvia Juliana
Torres-Sánchez, Luisa
Burguete-García, Ana I.
Orbe Orihuela, Yaneth Citlalli
Vázquez-Salas, Ruth Argelia
Álvarez-Topete, Esmeralda
Gómez, Rocío
author_sort Trujillo-Cáceres, Silvia Juliana
collection PubMed
description Sexually transmitted infections and its contribution to prostate cancer (PC) development have been relevant in different populations. MSMB gene polymorphism (rs10993994) has exhibited an association both with PC as well as the susceptibility to sexually transmitted infections. Hitherto, these conditions have been not studied in Mexico yet, neither if sexually transmitted infections could modify the MSMB and PC association. Herein, socio-demographic features, sexually transmitted infections records, the reproductive backgrounds, and the genetic characterisation were analysed in 322 incident PC cases and 628 population healthy controls from Mexico City. Whole PC, early-onset PC (PC at < 60 years old), late-onset PC (≥ 60 years old), and PC aggressiveness were used to evaluate the genetic variants contribution to PC risk using unconditional logistic regression models. Overall, none associations between the allelic variants of rs10993994 polymorphisms with whole and PC aggressiveness were found. Howbeit, the TT genotype carriers presented the highest susceptibility to develop early-onset PC (OR = 2.66; 95% CI = 1.41, 5.04; p = 0.03) than CC+CT carriers, both with codominant and recessive models. Although none association between whole PC and MSMB gene polymorphism was found, our results were reinforced by prior studies in European descendent populations, suggesting a contribution between rs10993994 and early-onset PC development.
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spelling pubmed-63668232019-02-15 Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males Trujillo-Cáceres, Silvia Juliana Torres-Sánchez, Luisa Burguete-García, Ana I. Orbe Orihuela, Yaneth Citlalli Vázquez-Salas, Ruth Argelia Álvarez-Topete, Esmeralda Gómez, Rocío Oncotarget Research Paper Sexually transmitted infections and its contribution to prostate cancer (PC) development have been relevant in different populations. MSMB gene polymorphism (rs10993994) has exhibited an association both with PC as well as the susceptibility to sexually transmitted infections. Hitherto, these conditions have been not studied in Mexico yet, neither if sexually transmitted infections could modify the MSMB and PC association. Herein, socio-demographic features, sexually transmitted infections records, the reproductive backgrounds, and the genetic characterisation were analysed in 322 incident PC cases and 628 population healthy controls from Mexico City. Whole PC, early-onset PC (PC at < 60 years old), late-onset PC (≥ 60 years old), and PC aggressiveness were used to evaluate the genetic variants contribution to PC risk using unconditional logistic regression models. Overall, none associations between the allelic variants of rs10993994 polymorphisms with whole and PC aggressiveness were found. Howbeit, the TT genotype carriers presented the highest susceptibility to develop early-onset PC (OR = 2.66; 95% CI = 1.41, 5.04; p = 0.03) than CC+CT carriers, both with codominant and recessive models. Although none association between whole PC and MSMB gene polymorphism was found, our results were reinforced by prior studies in European descendent populations, suggesting a contribution between rs10993994 and early-onset PC development. Impact Journals LLC 2019-01-22 /pmc/articles/PMC6366823/ /pubmed/30774776 http://dx.doi.org/10.18632/oncotarget.26592 Text en Copyright: © 2019 Trujillo-Cáceres et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Trujillo-Cáceres, Silvia Juliana
Torres-Sánchez, Luisa
Burguete-García, Ana I.
Orbe Orihuela, Yaneth Citlalli
Vázquez-Salas, Ruth Argelia
Álvarez-Topete, Esmeralda
Gómez, Rocío
Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title_full Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title_fullStr Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title_full_unstemmed Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title_short Contribution of MSMB promoter region gene polymorphism to early-onset prostate cancer risk in Mexican males
title_sort contribution of msmb promoter region gene polymorphism to early-onset prostate cancer risk in mexican males
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366823/
https://www.ncbi.nlm.nih.gov/pubmed/30774776
http://dx.doi.org/10.18632/oncotarget.26592
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