4.5 Review

Hereditary breast and ovarian cancer: from genes to molecular targeted therapies

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Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10408363.2023.2234488

Keywords

Hereditary breast cancer; hereditary ovarian cancer; BRCA1; BRCA2; PARP inhibitors; olapramib; niraparib; talazoparib; hereditary tumors; >

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Hereditary familial tumors account for 10-15% of all malignancies and offer important research models for personalized therapeutic approaches. Hereditary breast and ovarian cancer (HBOC) syndrome, associated with BRCA1 and BRCA2 mutations, is characterized by specific clinical criteria and can be diagnosed and managed through counseling and genetic testing. BRCA gene mutations have therapeutic implications, particularly in the treatment of breast cancer using PARP inhibitors.
Hereditary familial tumors constitute 10-15% of all malignancies and present opportunities for the identification of therapeutic approaches against specific germline genetic defects. Hereditary breast and ovarian cancer (HBOC) syndrome, which is linked to the pathogenic mutations of the breast cancer 1 (BRCA1) and breast cancer 2 (BRCA2) genes, is an important research model for personalized therapeutic approaches for specific germline mutations. HBOC is characterized by multiple cases of breast and ovarian carcinoma in association with other tumors (prostate, pancreas and stomach carcinoma) within the same family branch, a young age of onset (<36 years), bilaterality and an autosomal dominant pattern of inheritance. Counseling, evaluation of the clinical criteria for the diagnosis of HBOC, and the performance of genetic testing allow for the identification of subjects with BRCA1/2 mutations and provide crucial information for clinical and therapeutic management. The identification of a BRCA gene mutation has therapeutic implications for women with metastatic and non-metastatic breast cancer. In the therapeutic setting of BRCA+ breast cancer, treatment with poly (ADP-ribose) polymerase (PARP) inhibitors, which keep cancer cells from repairing their damaged DNA and cause cell death, is remarkable. This review summarizes the evidence demonstrating the value of BRCA1/2 status as a diagnostic and prognostic tool and as a predictive biomarker in the personalized approach to hereditary BRCA + cancers.

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