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Genetic polymorphisms of PPAR gamma, arsenic methylation capacity and breast cancer risk in Mexican women / Polimorfismos genéticos de PPAR gamma, capacidad de metilación del arsénico y riesgo de cáncer de mama en mujeres mexicanas
Pineda-Belmontes, Cristina P; Hernández-Ramírez, Raúl U; Hernández-Alcaraz, César; Cebrián, Mariano E; López-Carrillo, Lizbeth.
  • Pineda-Belmontes, Cristina P; Instituto Nacional de Salud Pública. Cuernavaca. MX
  • Hernández-Ramírez, Raúl U; Instituto Nacional de Salud Pública. Cuernavaca. MX
  • Hernández-Alcaraz, César; Instituto Nacional de Salud Pública. Cuernavaca. MX
  • Cebrián, Mariano E; Instituto Nacional de Salud Pública. Cuernavaca. MX
  • López-Carrillo, Lizbeth; Instituto Nacional de Salud Pública. Cuernavaca. MX
Salud pública Méx ; 58(2): 220-227, Mar.-Apr. 2016. tab
Article in English | LILACS | ID: lil-793000
ABSTRACT
Abstract

Objective:

To evaluate whether the presence of polymorphisms of peroxisome proliferator-activated receptor gamma PPARγ (Pro 1 2Ala) and PPARGC1B (Ala203Pro) modifies the association between the inorganic arsenic (iAs) methylation capacity and breast cancer (BC). Materials and

methods:

Mexican women were interviewed, and blood and urine samples were collected from them (cases/controls= 197/220). The concentration of urinary arsenic species and the polymorphisms of interest were determined by high-performance liquid chromatography with inductively coupled plasma mass spectrometry (HPLC-ICP-MS) and polymerase chain reaction (PCR), respectively.

Results:

In women with a high %MMA (urinary monomethyl arsenic) and high primary methylation ratio (PM = MMA/iAs), the risk of BC was increased (odds ratio [OR]%MMA T3 vs.T1= 3.60 95% confidence interval [CI] 2.02-6.41, ORPMI T3 vs.T1= 3.47 95%CI 1.95-6.17), which was maintained after adjusting for polymorphisms. No significant interactions were observed between the polymorphisms and the arsenic variables on the risk of BC.

Conclusion:

Pro 12Ala and Ala203Pro polymorphisms did not modify the association between the iAs methylation capacity and BC.
RESUMEN
Resumen

Objetivo:

Evaluar si la presencia de polimorfismos de PPARγ (Pro 1 2Ala) y PPARGC1B (Ala203Pro) modifica la asociación entre la capacidad de metilación del arsénico inorgánico (Asi) y el cáncer de mama (CM). Material y

métodos:

Se entrevistaron mujeres mexicanas y recolectaron muestras de sangre y orina de (casos/controles=197/220). La concentración de especies de arsénico urinario y los polimorfismos de interés se determinaron mediante cromatografía líquida de alta resolución acoplada a espectrometría de masas (HPLC-ICP-MS) y reacción en cadena de la polimerasa (PCR), respectivamente.

Resultados:

En mujeres con %MMA (monometilarsénico urinario) y razón de primera metilación altas (PM=MMA/Asi) se incrementó el riesgo de CM (RM%MMAT3vsT1=3.60 intervalo de confianza [IC]95%2.02-6.41, RMPMT3vs.T1=3.47IC95%1.95-6.17), que se mantuvo, respectivamente, al ajustar por polimorfismos. No se observaron interacciones significativas entre los polimorfismos y las variables arsenicales sobre el riesgo de CM.

Conclusión:

Los polimorfismos Pro 12Ala y Ala203Pro no modificaron la asociación entre la capacidad de metilación del Asi y el CM.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Arsenicals / Breast Neoplasms / Carrier Proteins / Polymorphism, Single Nucleotide / PPAR gamma Type of study: Etiology study / Observational study / Risk factors Limits: Adult / Aged / Female / Humans Country/Region as subject: Mexico Language: English Journal: Salud pública Méx Journal subject: Public Health Year: 2016 Type: Article Affiliation country: Mexico Institution/Affiliation country: Instituto Nacional de Salud Pública/MX

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Full text: Available Index: LILACS (Americas) Main subject: Arsenicals / Breast Neoplasms / Carrier Proteins / Polymorphism, Single Nucleotide / PPAR gamma Type of study: Etiology study / Observational study / Risk factors Limits: Adult / Aged / Female / Humans Country/Region as subject: Mexico Language: English Journal: Salud pública Méx Journal subject: Public Health Year: 2016 Type: Article Affiliation country: Mexico Institution/Affiliation country: Instituto Nacional de Salud Pública/MX