6533b862fe1ef96bd12c6c3f
RESEARCH PRODUCT
Prenatal exposure to mixtures of xenoestrogens and genome-wide DNA methylation in human placenta
Jesús IbarluceaGeòrgia EscaramísLoreto Santa-marinaValeria MottaMariona BustamanteValentina BollatiLucas A. SalasNadia VilahurJuan P. ArrebolaFerran BallesterMariana F. FernándezMario MurciaIsolina RiañoEva MoralesNicolas OleaAdonina TardónJordi SunyerXavier Estivillsubject
0301 basic medicineMaleCancer Researchmedicine.medical_specialtymedicine.medical_treatmentPlacentaADNBiologyEpigenesis GeneticAndrology03 medical and health scienceschemistry.chemical_compoundSex FactorsPregnancyPlacentaInternal medicineGeneticsmedicineBirth WeightHumansPrenatalLDL-Receptor Related Protein-Associated ProteinGeneTEXBEndocrine disruptorsDNA methylationEpigenome xenoestrogensRNA-Binding ProteinsEstrogensMethylationEpigenomeSteroid hormone030104 developmental biologyEndocrinologymedicine.anatomical_structureXenoestrogenCpG sitechemistryPrenatal Exposure Delayed EffectsDNA methylationKCNQ1 Potassium ChannelProgrammingCpG IslandsFemaleThiolester HydrolasesCarrier ProteinsGenome-Wide Association Studydescription
BACKGROUND: In utero exposure to xenostrogens may modify the epigenome. We explored the association of prenatal exposure to mixtures of xenoestrogens and genome-wide placental DNA methylation. MATERIALS & METHODS: Sex-specific associations between methylation changes in placental DNA by doubling the concentration of TEXB-alpha exposure were evaluated by robust multiple linear regression. Two CpG sites were selected for validation and replication in additional male born placentas. RESULTS: No significant associations were found, although the top significant CpGs in boys were located in the LRPAP1, HAGH, PPARGC1B, KCNQ1 and KCNQ1DN genes, previously associated to birth weight, Type 2 diabetes, obesity or steroid hormone signaling. Neither technical validation nor biological replication of the results was found in boys for LRPAP and PPARGC1B. CONCLUSION: Some suggestive genes were differentially methylated in boys in relation to prenatal xenoestrogen exposure, but our initial findings could not be validated or replicated. This work was part of the European-wide project Transportation Air pollution and Physical ActivitieS (TAPAS): an integrated health risk assessment program of climate change and urban policies, which had partners in Barcelona, Basel, Copenhagen, Paris, Prague, and Warsaw. TAPAS was a 4-year project funded by the Coca-Cola Foundation, AGAUR, and CREAL (http://www.tapas-program.org/). CREAL is part of CIBERESP (http://www.ciberesp.es/), the Spanish Network for Epidemiology and Public Health Research. CREAL and its members are based at and supported by the Universitat Pompeu Fabra (http://www.upf.edu/en/).
year | journal | country | edition | language |
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2015-12-19 |