| Literature DB >> 27581327 |
Anis Kaldawy1, Yakir Segev1, Ofer Lavie1, Ron Auslender1, Victoria Sopik2, Steven A Narod3.
Abstract
Epithelial ovarian cancers can be divided into the more common, aggressive type II cancers and the less common, slow-growing type I cancers. Under this model, serous ovarian carcinomas can be subdivided into high-grade (type II) and low-grade (type I) tumours. The two-tier system for grading serous ovarian carcinomas is superior to more detailed grading systems in terms of predicting survival. Low-grade serous carcinomas typically present in young women and have a relatively good prognosis, despite being resistant to chemotherapy. Low-grade serous cancers have a high prevalence of KRAS and BRAF mutations, but a low prevalence of TP53 mutations (which are characteristic of high-grade serous cancers). Among women with low-grade serous ovarian cancer, the presence of a KRAS/BRAF mutation is a favorable prognostic factor. Studies of the mitogen-activated protein kinase (MAPK) inhibitor in low-grade serous ovarian cancer suggest that identifying MAPK mutations might eventually be useful in guiding treatment.Entities:
Keywords: BRAF mutations; Epithelial ovarian cancer; High-grade serous ovarian cancer; Low-grade serous ovarian cancer; MAPK inhibitors
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Year: 2016 PMID: 27581327 DOI: 10.1016/j.ygyno.2016.08.320
Source DB: PubMed Journal: Gynecol Oncol ISSN: 0090-8258 Impact factor: 5.482