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Androgen receptor CAG polymorphism and sporadic and early-onset prostate cancer among Mexican men.
Gómez, Rocío; Torres-Sánchez, Luisa; Camacho-Mejorado, Rafael; Burguete-García, Ana I; Vázquez-Salas, Ruth Argelia; Martínez-Nava, Gabriela A; Santana, Carla; Noris, Gino.
Afiliación
  • Gómez R; Departamento de Toxicología. Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Mexico DF, México.
  • Torres-Sánchez L; Instituto Nacional de Salud Pública, Centro de Investigación en Salud Poblacional, Cuernavaca, México.
  • Camacho-Mejorado R; Departamento de Toxicología. Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Mexico DF, México.
  • Burguete-García AI; Instituto Nacional de Salud Pública, Centro de Investigación en Enfermedades Infecciosas, Cuernavaca, México.
  • Vázquez-Salas RA; Instituto Nacional de Salud Pública, Centro de Investigación en Salud Poblacional, Cuernavaca, México.
  • Martínez-Nava GA; Instituto Nacional de Salud Pública, Centro de Investigación en Enfermedades Infecciosas, Cuernavaca, México.
  • Santana C; Instituto Nacional de Rehabilitación 'Luis Guillermo Ibarra', Laboratorio de Líquido Sinovial, Mexico DF, México.
  • Noris G; Laboratorio BIMODI (Biología Molecular Diagnóstica), Santiago de Querétaro, México.
J Hum Genet ; 61(9): 781-6, 2016 Sep.
Article en En | MEDLINE | ID: mdl-27193223
ABSTRACT
A short CAG repeat length in the gene encoding for the androgen receptor (AR) has been associated with prostate cancer (PC) risk and aggressiveness. In Latino men, information on this association is scarce. Hence, the aim of this study was to evaluate this association in Mexican males. Using fragment analysis by capillary electrophoresis, we determined the number of CAG repeats-(CAG)n-in AR gene from 158 incident PC cases and 326 age-matched healthy controls (±5 years), residing in Mexico City, Mexico. According to Gleason scale and age at diagnosis, cases were classified as high (⩾7) and low grade (<7), as well as early onset (<60 years) or late onset PC (⩾60 years). At diagnosis, 78% of cases were classified as high-grade and 26.6% as early onset. Men with sporadic (no family history of PC) and early-onset PC presented shorter CAG repeat length than controls (18.6±2.2 vs 19.5±2.5; P=0.02). Lower number of CAG repeats (CAG)⩽19 were associated with a greater risk for early-onset PC (odds ratio 2.31; 95% confidence interval 1.14-4.69). CAG repeat length could increase the risk for sporadic and early-onset PC. The best cutoff point for identifying at-risk subjects was (CAG)19. However, further studies are necessary to replicate our findings in subjects with a family history of PC and also to evaluate the association between CAG repeats length and disease progression.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Neoplasias de la Próstata / Receptores Androgénicos / Repeticiones de Trinucleótidos Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged País/Región como asunto: Mexico Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Neoplasias de la Próstata / Receptores Androgénicos / Repeticiones de Trinucleótidos Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged País/Región como asunto: Mexico Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article
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