Genetic Links between Endometriosis and Endometriosis-Associated Ovarian Cancer-A Narrative Review (Endometriosis-Associated Cancer)

被引:1
|
作者
Pejovic, Tanja [1 ]
Cathcart, Ann M. [2 ]
Alwaqfi, Rofieda [3 ]
Brooks, Marjorie N. [1 ]
Kelsall, Rachel [4 ]
Nezhat, Farr R. [3 ,5 ,6 ]
机构
[1] Providence Med Ctr, Dept Obstet & Gynecol, Medford, OR 97504 USA
[2] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Portland, OR 97201 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol & Lab Med, New York, NY 10065 USA
[4] Pacific Northwest Univ Hlth Sci, Yakima, WA 98901 USA
[5] Cornell Univ, Weill Cornell Med Coll, New York, NY 10065 USA
[6] NYU, Long Isl Sch Med, Mineola, NY 11501 USA
来源
LIFE-BASEL | 2024年 / 14卷 / 06期
关键词
endometriosis; cancer; ARD1A; ovarian cancer; clear-cell carcinoma; endometrioid adenocarcinoma; CLEAR-CELL CARCINOMA; ATYPICAL ENDOMETRIOSIS; CLINICAL-IMPLICATIONS; ANTITUMOR-ACTIVITY; ARID1A MUTATIONS; RISK; ADENOCARCINOMA; EXPRESSION; CLASSIFICATION; EMPHASIS;
D O I
10.3390/life14060704
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Endometriosis is a frequent, estrogen-dependent, chronic disease, characterized by the presence of endometrial glands and stroma outside of the uterine cavity. Although it is not considered a precursor of cancer, endometriosis is associated with ovarian cancer. In this review, we summarized the evidence that clear-cell and endometrioid ovarian carcinomas (endometriosis-associated ovarian carcinoma-EAOC) may arise in endometriosis. The most frequent genomic alterations in these carcinomas are mutations in the AT-rich interaction domain containing protein 1A (ARID1A) gene, a subunit of the SWI/SNF chromatin remodeling complex, and alterations in phosphatidylinositol 3-kinase (PI3K) which frequently coexist. Recent studies have also suggested the simultaneous role of the PTEN tumor-suppressor gene in the early malignant transformation of endometriosis and the contribution of deficient MMR (mismatch repair) protein status in the pathogenesis of EAOC. In addition to activating and inactivating mutations in cancer driver genes, the complex pathogenesis of EAOC involves multiple other mechanisms such as the modulation of cancer driver genes via the transcriptional and post-translational (miRNA) modulation of cancer driver genes and the interplay with the inflammatory tissue microenvironment. This knowledge is being translated into the clinical management of endometriosis and EAOC. This includes the identification of the new biomarkers predictive of the risk of endometriosis and cancer, and it will shape the precision oncology treatment of EAOC.
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页数:15
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