Article ; Online: BRCA2 Polymorphisms and Breast Cancer Susceptibility: a Multi-Tools Bioinformatics Approach.
2024 Volume 58, Issue 2, Page(s) 128–143
Abstract: Background/aims: The main focus of this investigation is to identify deleterious single nucleotide polymorphisms (SNPs) located in the BRCA2 gene through in silico approach, thereby,providing an understanding of potential consequences regarding the ... ...
Abstract | Background/aims: The main focus of this investigation is to identify deleterious single nucleotide polymorphisms (SNPs) located in the BRCA2 gene through in silico approach, thereby,providing an understanding of potential consequences regarding the susceptibility to breast cancer. Methods: The GenomAD database was used to identify SNPs. To determine the potential adverse consequences, our study employed various prediction tools, including SIFT, PolyPhen, PredictSNP, SNAP2, PhD-SNP, and ClinVar. The pathogenicity associated with the deleterious snSNPs was evaluated bu MutPred and Fathmm. Additionally, I-Mutant and MuPro were used to assess the stability, followed by conservation and protein-protein interaction analysis using robust computational tools. The 3D structure of BRCA2 protein was generated by SwissModel, followed by validation using PROCHECK and Errat. Results: The GenomAD database was used to identify a total of 7, 921 SNPs, including 1940 missense SNPs. A set of 69 SNPs predicted by consensus to be damaging across all platforms was identified. Mutpred and Fathmm identified 48 and 38 SNPs, respectively to be associated with cancer. While I- Mutant and MuPro assays suggested 22 SNPs to decrease protein stability. Additionally, these 22 SNPs reside within highly conserved regions of the BRCA2 protein. Domain analysis, utilizing InterPro, pinpointed 18 deleterious mutations within crucial DNA binding domains and one in the BRC repeat region. Conclusion: This study establishes a foundation for future experimental validations and the creation of breast cancer-targeted treatment approaches. |
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MeSH term(s) | Humans ; Female ; BRCA2 Protein/genetics ; Genes, BRCA2 ; Breast Neoplasms/genetics ; Polymorphism, Single Nucleotide ; Computational Biology |
Chemical Substances | BRCA2 Protein ; BRCA2 protein, human |
Language | English |
Publishing date | 2024-03-26 |
Publishing country | Germany |
Document type | Journal Article |
ZDB-ID | 1067572-3 |
ISSN | 1421-9778 ; 1015-8987 |
ISSN (online) | 1421-9778 |
ISSN | 1015-8987 |
DOI | 10.33594/000000689 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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