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Oral Contraceptive Use May Modulate Global Genomic DNA Methylation and Promoter Methylation of APC1 and ESR1

BACKGROUND: There are challenging reports in the public health sphere regarding associations between oral contraceptive (OC) use and cancer risk. METHODS: To evaluate possible effects of OCs on cancer susceptibility, we quantified of global 5-methyl cytosine (5-mC) levels and assessed methylation pa...

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Detalles Bibliográficos
Autores principales: Sarabi, Mostafa Moradi, Ghareghani, Parvin, Khademi, Fatemeh, Zal, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720637/
https://www.ncbi.nlm.nih.gov/pubmed/28950679
http://dx.doi.org/10.22034/APJCP.2017.18.9.2361
Descripción
Sumario:BACKGROUND: There are challenging reports in the public health sphere regarding associations between oral contraceptive (OC) use and cancer risk. METHODS: To evaluate possible effects of OCs on cancer susceptibility, we quantified of global 5-methyl cytosine (5-mC) levels and assessed methylation patterns of CpG islands of two key tumor suppressor genes, APC1 and ESR1, in serum of users by enzyme-linked immunosorbent assay and methylation specific PCR methods, respectively. RESULTS: Our results indicated that OCs significantly decrease the level of global DNA methylation in users relative to control non-users. However, our data revealed no significant differences between CpG island methylation patterns for ESR1 and APC1 in healthy control and OC-treated women. However, we did find a trend for hypermethylation of both tumor suppressor genes in OC users. CONCLUSION: Our data suggest that the level of 5-mC but not individual CpG island patterns is significantly influenced by OCs in our cross-section of adult users.