Your browser doesn't support javascript.
loading
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.
Afiliação
  • Trujillo-Cáceres SJ; Centro de Investigación en Salud Poblacional, Instituto Nacional de Salud Pública (INSP), Cuernavaca, Morelos, Mexico.
  • Torres-Sánchez L; Centro de Investigación en Salud Poblacional, Instituto Nacional de Salud Pública (INSP), Cuernavaca, Morelos, Mexico.
  • Burguete-García AI; Centro de Investigación en Enfermedades Infecciosas, INSP, Cuernavaca, Morelos, Mexico.
  • Orbe Orihuela YC; Centro de Investigación en Enfermedades Infecciosas, INSP, Cuernavaca, Morelos, Mexico.
  • Vázquez-Salas RA; Conacyt-Centro de Investigación en Salud Poblacional, INSP, Cuernavaca, Morelos, Mexico.
  • Álvarez-Topete E; Departamento de Toxicología, Cinvestav-IPN, Mexico City, Mexico.
  • Gómez R; Departamento de Toxicología, Cinvestav-IPN, Mexico City, Mexico.
Oncotarget ; 10(7): 738-748, 2019 Jan 22.
Article em En | MEDLINE | ID: mdl-30774776
ABSTRACT
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.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies País como assunto: Mexico Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies País como assunto: Mexico Idioma: En Ano de publicação: 2019 Tipo de documento: Article