» Articles » PMID: 28546758

Distinct Implications of Different BRCA Mutations: Efficacy of Cytotoxic Chemotherapy, PARP Inhibition and Clinical Outcome in Ovarian Cancer

Overview
Publisher Dove Medical Press
Specialty Oncology
Date 2017 May 27
PMID 28546758
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Approximately a fifth of ovarian carcinoma (OC) is associated with inherited germline mutations, most commonly in the DNA repair genes or (). - and -associated OCs have historically been described as a single subgroup of OC that displays a distinct set of characteristics termed the "BRCAness" phenotype. The hallmarks of this phenotype are superior clinical outcome and hypersensitivity to platinum-based chemotherapy and poly-(ADP-ribose) polymerase (PARP) inhibitors. However, growing evidence suggests that - and -associated OCs display distinct characteristics, most notably in long-term patient survival. Furthermore, recent data indicate that the site of mutation is important with regard to platinum and PARP inhibitor sensitivity. Here, we summarize the body of research describing the BRCAness phenotype and highlight the differential implications of different mutations with regard to clinicopathologic features, therapy sensitivity and clinical outcome in OC.

Citing Articles

Robotic Rectosigmoid Resection with Totally Intracorporeal Colorectal Anastomosis (TICA) for Recurrent Ovarian Cancer: A Case Series and Description of the Technique.

Gallotta V, Palmieri L, Santullo F, Certelli C, Lodoli C, Abatini C J Pers Med. 2024; 14(10).

PMID: 39452559 PMC: 11508377. DOI: 10.3390/jpm14101052.


RFWD3 modulates response to platinum chemotherapy and promotes cancer associated phenotypes in high grade serous ovarian cancer.

Taylor S, Hollis R, Gourley C, Herrington C, Langdon S, Arends M Front Oncol. 2024; 14:1389472.

PMID: 38711848 PMC: 11071161. DOI: 10.3389/fonc.2024.1389472.


Confirmation of the utility of the CA-125 elimination rate (KELIM) as an indicator of the chemosensitivity in advanced-stage ovarian cancer in a "real-life setting".

van Wagensveld L, Colomban O, van der Aa M, Freyer G, Sonke G, Kruitwagen R J Gynecol Oncol. 2024; 35(3):e34.

PMID: 38216134 PMC: 11107274. DOI: 10.3802/jgo.2024.35.e34.


Should We Abandon Intraperitoneal Chemotherapy in the Treatment of Advanced Ovarian Cancer? A Meta-Analysis.

Climent M, Serra A, Balaguer C, Llueca A J Pers Med. 2023; 13(12).

PMID: 38138863 PMC: 10745120. DOI: 10.3390/jpm13121636.


Development of Homologous Recombination Functional Assays for Targeting the DDR.

Oswald A, Gourley C Cancer Treat Res. 2023; 186:43-70.

PMID: 37978130 DOI: 10.1007/978-3-031-30065-3_4.


References
1.
Harter P, Johnson T, Berton-Rigaud D, Park S, Friedlander M, Del Campo J . BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study. Gynecol Oncol. 2016; 140(3):443-9. DOI: 10.1016/j.ygyno.2015.12.027. View

2.
Gourley C, Michie C, Roxburgh P, Yap T, Harden S, Paul J . Increased incidence of visceral metastases in scottish patients with BRCA1/2-defective ovarian cancer: an extension of the ovarian BRCAness phenotype. J Clin Oncol. 2010; 28(15):2505-11. DOI: 10.1200/JCO.2009.25.1082. View

3.
Xu B, Kim St , Kastan M . Involvement of Brca1 in S-phase and G(2)-phase checkpoints after ionizing irradiation. Mol Cell Biol. 2001; 21(10):3445-50. PMC: 100266. DOI: 10.1128/MCB.21.10.3445-3450.2001. View

4.
Davies A, Masson J, McIlwraith M, Stasiak A, Stasiak A, Venkitaraman A . Role of BRCA2 in control of the RAD51 recombination and DNA repair protein. Mol Cell. 2001; 7(2):273-82. DOI: 10.1016/s1097-2765(01)00175-7. View

5.
Drost R, Dhillon K, van der Gulden H, van der Heijden I, Brandsma I, Cruz C . BRCA1185delAG tumors may acquire therapy resistance through expression of RING-less BRCA1. J Clin Invest. 2016; 126(8):2903-18. PMC: 4966325. DOI: 10.1172/JCI70196. View