Cell cycle, apoptosis, cell differentiation, and lipid metabolism gene expression in endometriotic tissue and exposure to parabens and benzophenones
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Peinado Rodríguez, Francisco Manuel; Olivas Martínez, Alicia; Iribarne Durán, Luz María; Ubiña, Alfredo; León, Josefa; Vela Soria, Fernando; Fernández Parra, Jorge; Fernández Cabrera, Mariana Fátima; Olea Serrano, Nicolás; Freire, Carmen; Ocón Hernández, Olga; Artacho Cordón, FranciscoMateria
Parabens Benzophenones Endometriosis Cell cycle Cell differentiation Lipid metabolism
Date
2023-03-30Abstract
Aim: To describe the expression profile in endometriotic tissue of genes involved in four signaling pathways related to
the development and progression of endometriosis (cell cycle, apoptosis, cell differentiation and lipid metabolism) and
to explore its relationship with the women exposure to chemicals with hormonal activity released from cosmetics and
personal care products (PCPs).
Methods: This cross-sectional study, encompassed within the EndEA study, comprised a subsample of 33 women with
endometriosis. Expression levels of 13 genes (BMI1, CCNB1, CDK1, BAX, BCL2L1, FOXO3, SPP1, HOXA10, PDGFRA,
SOX2, APOE, PLCG1 and PLCG2) in endometriotic tissue and urinary concentrations of 4 paraben (PB) and 3 benzophenone
(BP) congeners were quantified. Bivariate linear and logistic regression analyses were performed to explore
the associations between exposure and gene expression levels.
Results: A total of 8 out 13 genes (61.5%) were expressed in >75% of the samples. Exposure to congeners of PBs and/
or BPs was associated with the overexpression of CDK1 gene (whose protein drives cells through G2 phase and mitosis),
HOXA10 and PDGFRA genes (whose proteins favor pluripotent cell differentiation to endometrial cells), and APOE
(whose protein regulates the transport and metabolism of cholesterol, triglycerides and phospholipids in multiple tissues)
and PLCG2 genes (whose protein creates 1D-myo-inositol 1,4,5-trisphosphate and diacylglycerol, two important
second messengers).
Conclusions: Our findings suggest that women exposure to cosmetic and PCP-released chemicals might be associated
with the promotion of cell cycle and cell differentiation as well as with lipid metabolism disruption in endometriotic
tissue, three crucial signaling pathways in the development and progression of endometriosis. However, further studies
should be accomplished to confirm these preliminary data.