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Tailoring Ovarian Cancer Treatment: Implications of BRCA1/2 Mutations

Title Tailoring Ovarian Cancer Treatment: Implications of BRCA1/2 Mutations
Authors Ainhoa Madariaga, Stephanie Lheureux, Amit M. Oza
Magazine Cancers
Date 03/23/2019
DOI 10.3390/cancers11030416
Introduction High grade serous ovarian cancer (HGSOC) is the most prevalent form of epithelial ovarian cancer, characterised by over 20% germline or somatic mutations in BRCA1 and BRCA2 tumour suppressor genes. These genes play critical roles in DNA damage repair through homologous recombination (HR) and transcription regulation. BRCA mutations result in unique responses to DNA-damaging treatments, such as platinum-based chemotherapy and poly-ADP ribose polymerase inhibitors (PARPi). Resistance mechanisms to these treatments have emerged, including enhanced HR through reverse BRCA mutations, changes in non-homologous end-joining (NHEJ) repair, and drug efflux pumps. Current ovarian cancer therapies, encompassing surgery, chemotherapy, targeted treatments, and maintenance strategies, as well as emerging resistance mechanisms, are examined, with a focus on future treatment trends for BRCA mutation carriers.
Quote Madariaga, A.; Lheureux, S.; Oza, A. M. Customising Ovarian Cancer Treatment: Implications of BRCA1/2 Mutations. Cancers 2019, 11, 3, 416.
Element Platinum (Pt)
Topics Biomedical Materials
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