Detection of hypermethylation BRCA1/2 gene promoter in breast tumours among Moroccan women.

Mol Biol Rep

Team of Virology, Oncology and Medical Biotechnologies, Laboratory of Virology, Microbiology, Quality and Biotechnologies/ETB, Faculty of Sciences and Technics-Mohammedia, University Hassan II of Casablanca, Po Box 146, Mohammedia, Morocco.

Published: November 2021

AI Article Synopsis

  • The study investigates the relationship between hypermethylation of the BRCA1/2 promoter genes and breast cancer in women, focusing on how this relates to age and tumor stage.
  • It analyzes DNA from 50 biopsies of Moroccan women with breast cancer, revealing that 62% of samples showed BRCA1 hypermethylation, while BRCA2 was negative.
  • The findings suggest that BRCA1 methylation is more prevalent in women over 47 years old, indicating that age could play a significant role in the progression of breast cancer.

Article Abstract

Background: The promoter region is a key element of gene expression regulation. In mammals, most of the genes present, at the level of their promoter, a large number of islands CpG. Age also is seen as another factor for developing breast cell cancer reaching the tumour stage.

Aim: This study aimed to explore the hypermethylation of the BRCA1/2 promoter gene in women breast cancer and correlation with age and tumour stage.

Materials And Methods: Fifty biopsies were derived from Moroccan women treated for breast carcinoma, the DNA extracted was treated by bisulphite and the targeted BRCA1/2 Amplicons were amplified by specific methylation primers (MSP).

Results: The result shows that 62% of the samples were BRCA1 methylated in addition and negative result for BRCA2, these positive epigenetic factor were remarkable in women over 47 years and at the stage of malignant tumour.

Conclusion: These results show that half of the methylated samples are positive with a majority of over 47 years old, and confirms that age might be an additional factor for breast cancer development.

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Source
http://dx.doi.org/10.1007/s11033-021-06705-2DOI Listing

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