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.

Prenatal exposure to mixtures of xenoestrogens and genome-wide DNA methylation in human placenta / N. Vilahur, M. Bustamante, E. Morales, V. Motta, M.F. Fernandez, L.A. Salas, G. Escaramis, F. Ballester, M. Murcia, A. Tardon, I. Riaño, L. Santa Marina, J. Ibarluzea, J.P. Arrebola, X. Estivill, V. Bollati, J. Sunyer, N. Olea. - In: EPIGENOMICS. - ISSN 1750-1911. - 81:1(2016 Jan), pp. 43-54. [10.2217/epi.15.91]

Prenatal exposure to mixtures of xenoestrogens and genome-wide DNA methylation in human placenta

V. Motta;V. Bollati;
2016

Abstract

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.
DNA methylation; TEXB; endocrine disruptors; epigenome xenoestrogens; placenta; prenatal; programming
Settore MED/44 - Medicina del Lavoro
gen-2016
18-dic-2015
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/349960
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