New Insights into the Molecular Mechanisms of Endometriosis and Endometriosis-associated Cancer
This review highlights key mutational hallmarks, epigenetic modifications, and gene expression changes driving endometriosis development and its malignant transformation to ovarian cancer.
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This review article examines the molecular mechanisms driving endometriosis and its potential malignant transformation into ovarian cancer, specifically clear cell and endometrioid carcinomas. The authors highlight that while endometriosis is benign, it carries an elevated cancer risk supported by the identification of somatic mutations in the PI3K/mTOR pathway and ARID1A within histologically normal tissue. The paper summarizes key findings regarding mutational hallmarks, epigenetic modifications, and gene expression changes that contribute to disease development and progression in the context of inflammatory and hormone-dependent processes. This paper is centrally about endometriosis — specifically the molecular basis of the condition and its association with endometriosis-associated ovarian cancers.
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