ARID1a Gene as a Potential Early Marker to Tackle Endometriosis-Associated Ovarian Cancer
- PMID: 38029403
- PMCID: PMC11567265
- DOI: 10.14336/AD.2023.1109
ARID1a Gene as a Potential Early Marker to Tackle Endometriosis-Associated Ovarian Cancer
Abstract
The worries of women with endometriosis - a chronic gynecological disease affecting approximately 10% of women of childbearing age - about the increased risk of ovarian cancer are present worldwide. Endometriosis is a common, often painful, but benign gynecological disease that affects women. However, the pathogenesis remains elusive but is certainly multifactorial. Interestingly, endometriosis shares similarities with cancer. Therefore, women suffering from endometriosis fear an increased risk of ovarian cancer. In addition, these patients suffer from anxiety and depression. Previous studies have provided evidence that epithelial mutations in endometriosis or in the endometrium include certain inactivating mutations responsible for ovarian cancer, such as in the ARID1A gene.
Conflict of interest statement
The Authors declare no Competing Financial or Non-Financial Interests.
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References
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- Kvaskoff M, Horne AW, Missmer SA (2017). Informing women with endometriosis about ovarian cancer risk. Lancet. 390(10111):2433-2434. - PubMed
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- Kinose Y, Xu H, Kim H, Kumar S, Shan X, George E, et al..(2023). Dual blockade of BRD4 and ATR/WEE1 pathways exploits ARID1A loss in clear cell ovarian cancer. Res Sq, 27:rs.3.rs-3314138.
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