Breast cancer remains the most common female cancer worldwide. The majority will arise spontaneously, with almost a third having a heritable component. Approximately 5–10% of all breast cancers will have a strong inherited element with pathogenic variants in the BRCA1 and BRCA2 amongst the most studied breast cancer genes. An overview of breast cancer is provided with references to the clinical and pathological features in BRCA1 and BRCA2 related cancers. The roles of PARP inhibitors and immunotherapy are discussed. The management of healthy individuals harbouring a pathogenic variant in the two genes is reviewed and future directions considered
Tumor suppressor genes that perform apparently generic cellular functions nonetheless cause tissue-s...
AbstractA large number of diverse functions have been attributed to the BRCA1 and BRCA2 breast cance...
Background:Both BRCA1 and BRCA2 are tumor suppressor gene and are inherited as an autosomal dominant...
Breast cancer is the most common cancer among women in Poland and worldwide, second only to lung can...
The biology of breast cancer is complex, and the increasing knowledge of its molecular biology is ha...
Patients with germline mutations in BRCA1 or BRCA2 genes are predisposed to breast cancer. The BRCA1...
In the human genome, BRCA1 and BRCA2 (for BReast CAncer 1 and 2) genes encode for proteins involved ...
Breast cancer patients with BRCA1/2-driven tumors may benefit from targeted therapy. It is not clear...
Breast cancer patients with BRCA1/2‐driven tumors may benefit from targeted therapy. It is not clear...
Purpose : The morphologic and molecular phenotype of breast cancers may help identify patients who a...
The contribution of germline copy number variants (CNVs) to risk of developing cancer in individuals...
Women who carry a pathogenic mutation in the breast cancer susceptibility genes BRCA1 or BRCA2 (BRCA...
Abstract Germline mutations in BRCA1 and BRCA2 (BRCA) genes confer high risk of developing cancer, e...
Mutations in two major breast cancer susceptibility genes, BRCA1 and BRCA2, have been identified to ...
Background: In kindreds carrying path_BRCA1/2 variants, some women in these families will develop ca...
Tumor suppressor genes that perform apparently generic cellular functions nonetheless cause tissue-s...
AbstractA large number of diverse functions have been attributed to the BRCA1 and BRCA2 breast cance...
Background:Both BRCA1 and BRCA2 are tumor suppressor gene and are inherited as an autosomal dominant...
Breast cancer is the most common cancer among women in Poland and worldwide, second only to lung can...
The biology of breast cancer is complex, and the increasing knowledge of its molecular biology is ha...
Patients with germline mutations in BRCA1 or BRCA2 genes are predisposed to breast cancer. The BRCA1...
In the human genome, BRCA1 and BRCA2 (for BReast CAncer 1 and 2) genes encode for proteins involved ...
Breast cancer patients with BRCA1/2-driven tumors may benefit from targeted therapy. It is not clear...
Breast cancer patients with BRCA1/2‐driven tumors may benefit from targeted therapy. It is not clear...
Purpose : The morphologic and molecular phenotype of breast cancers may help identify patients who a...
The contribution of germline copy number variants (CNVs) to risk of developing cancer in individuals...
Women who carry a pathogenic mutation in the breast cancer susceptibility genes BRCA1 or BRCA2 (BRCA...
Abstract Germline mutations in BRCA1 and BRCA2 (BRCA) genes confer high risk of developing cancer, e...
Mutations in two major breast cancer susceptibility genes, BRCA1 and BRCA2, have been identified to ...
Background: In kindreds carrying path_BRCA1/2 variants, some women in these families will develop ca...
Tumor suppressor genes that perform apparently generic cellular functions nonetheless cause tissue-s...
AbstractA large number of diverse functions have been attributed to the BRCA1 and BRCA2 breast cance...
Background:Both BRCA1 and BRCA2 are tumor suppressor gene and are inherited as an autosomal dominant...