Salud Pública de México · 2016 · 25 citations · 26 references
Life SciencesGeneticsOncologyCancer PreventionGenetic EpidemiologyMedical GeneticsArsenic ToxicologyBiomarkers Of Genotoxic ExposureBreast Cancer Risk AssessmentGenetic Risk AssessmentHeavy Metal Risk AssessmentArsenic Exposure AssessmentArsenic Risk AssessmentBiomarkers Of Arsenic ExposureGenetic PolymorphismsMethylated Arsenic CompoundsMethylation CapacityPeroxisome Proliferator-activated Receptor Gamma RegulationPeroxisome Proliferator-activated Receptor Genetics
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.
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Terminal Differentiation of Human Breast Cancer through PPARγ
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