Endometriosis-associated ovarian carcinomas: insights into pathogenesis, diagnostics, and therapeutic targets-a narrative review

被引:54
作者
Samartzis, Eleftherios P. [1 ,2 ]
Labidi-Galy, S. Intidhar [3 ,4 ]
Moschetta, Michele [5 ]
Uccello, Mario [6 ]
Kalaitzopoulos, Dimitrios R. [1 ,2 ,7 ]
Perez-Fidalgo, J. Alejandro [8 ]
Boussios, Stergios [9 ,10 ]
机构
[1] Univ Hosp Zurich, Dept Gynecol, Frauenklinikstr 10, CH-8091 Zurich, Switzerland
[2] Univ Hosp Zurich, Gynecol Canc Ctr, Frauenklinikstr 10, CH-8091 Zurich, Switzerland
[3] Hop Univ Geneve, Dept Oncol, Geneva, Switzerland
[4] Univ Geneva, Dept Med, Fac Med, Geneva, Switzerland
[5] Cambridge Univ Hosp NHS Fdn Trust, Cambridge, England
[6] Northampton Gen Hosp NHS Trust, Northampton, England
[7] Kantonsspital Schaffhausen, Dept Gynecol & Obstet, Schaffhausen, Switzerland
[8] Hosp Clin Univ Valencia, INCLIVA, CIBERONC, Dept Med Oncol, Valencia, Spain
[9] Medway NHS Fdn Trust, Dept Med Oncol, Gillingham, Kent, England
[10] AELIA Org, 9th Km Thessaloniki Thermi, Thessaloniki, Greece
关键词
Ovarian cancer; endometriosis; clear cell ovarian carcinoma; endometrioid ovarian carcinoma; ARID1A mutations; PI3K/AKT/mTOR pathway; synthetic lethality; treatment; SWI/SNF transcription complex; HOSPITAL DISCHARGE DIAGNOSIS; CANCER-ASSOCIATED MUTATIONS; ARID1A PROTEIN EXPRESSION; REMODELING GENE ARID1A; CLEAR-CELL CARCINOMA; EPITHELIAL OVARIAN; SOMATIC MUTATIONS; PATHWAY ALTERATIONS; ANTITUMOR-ACTIVITY; TUMOR PROGRESSION;
D O I
10.21037/atm-20-3022a
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endometriosis is a benign gynecologic condition affecting up to one woman out of ten of reproductive age. It is defined by the presence of endometrial-like tissue in localizations outside of the uterine cavity. It often causes symptoms such as chronic pain, most frequently associated with the menstrual cycle, and infertility, but may also be oligoor asymptomatic. There is evidence that some ovarian carcinoma (OC) histotypes, mainly the ovarian clear cell (OCCC) and endometrioid (EnOC) carcinoma, may arise from endometriosis. The most frequent genomic alterations in these carcinomas are mutations in the AT-rich interacting domain containing protein 1A (ARID1A) gene, a subunit of the SWI/SNF chromatin remodeling complex, and alterations in the phosphatidylinositol 3-kinase (PI3K)/AKT/mTOR pathway, which frequently co-occur. In ARID1A deficient cancers preclinical experimental data suggest different targetable mechanisms including epigenetic regulation, cell cycle, genomic instability, the PI3K/AKT/mTOR pathway, inflammatory pathways, immune modulation, or metabolic alterations as potential precision oncology approaches. Most of these strategies are relying on the concept of synthetic lethality in which tumors deficient in ARID1A are more sensitive to the different compounds. Some of these approaches are currently being or have recently been investigated in early clinical trials. The remarkably frequent occurrence of these mutations in endometriosisassociated ovarian cancer, the occurrence in a relatively young population, and the high proportion of platinumresistant disease certainly warrants further investigation of precision oncology opportunities in this population. Furthermore, advanced knowledge about oncogenic mutations involved in endometriosis-associated ovarian carcinomas may be potentially useful for early cancer detection. However, this approach may be complicated by the frequent occurrence of somatic mutations in benign endometriotic tissue as recent studies suggest. In this narrative review of the current literature, we will discuss the data available on endometriosis-associated ovarian carcinoma, with special emphasis on epidemiology, diagnosis and molecular changes that could have therapeutic implications and clinical applicability in the future.
引用
收藏
页数:20
相关论文
共 151 条
[1]   ARID1A expression loss in gastric cancer: pathway-dependent roles with and without Epstein-Barr virus infection and microsatellite instability [J].
Abe, Hiroyuki ;
Maeda, Daichi ;
Hino, Rumi ;
Otake, Yuya ;
Isogai, Maya ;
Ushiku, Aya Shinozaki ;
Matsusaka, Keisuke ;
Kunita, Akiko ;
Ushiku, Tetsuo ;
Uozaki, Hiroshi ;
Tateishi, Yoko ;
Hishima, Tsunekazu ;
Iwasaki, Yoshiaki ;
Ishikawa, Shumpei ;
Fukayama, Masashi .
VIRCHOWS ARCHIV, 2012, 461 (04) :367-377
[2]   Cancer-Associated Mutations in Endometriosis without Cancer [J].
Anglesio, M. S. ;
Papadopoulos, N. ;
Ayhan, A. ;
Nazeran, T. M. ;
Noe, M. ;
Horlings, H. M. ;
Lum, A. ;
Jones, S. ;
Senz, J. ;
Seckin, T. ;
Ho, J. ;
Wu, R. -C. ;
Lac, V. ;
Ogawa, H. ;
Tessier-Cloutier, B. ;
Alhassan, R. ;
Wang, A. ;
Wang, Y. ;
Cohen, J. D. ;
Wong, F. ;
Hasanovic, A. ;
Orr, N. ;
Zhang, M. ;
Popoli, M. ;
McMahon, W. ;
Wood, L. D. ;
Mattox, A. ;
Allaire, C. ;
Segars, J. ;
Williams, C. ;
Tomasetti, C. ;
Boyd, N. ;
Kinzler, K. W. ;
Gilks, C. B. ;
Diaz, L. ;
Wang, T. -L. ;
Vogelstein, B. ;
Yong, P. J. ;
Huntsman, D. G. ;
Shih, I. -M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (19) :1835-1848
[3]   Clear cell carcinoma of the ovary: A report from the first Ovarian Clear Cell Symposium, June 24th, 2010 [J].
Anglesio, Michael S. ;
Carey, Mark S. ;
Koebel, Martin ;
MacKay, Helen ;
Huntsman, David G. .
GYNECOLOGIC ONCOLOGY, 2011, 121 (02) :407-415
[4]  
[Anonymous], 2016, J CLIN ONCOL S
[5]   Loss of ARID1A Expression Is an Early Molecular Event in Tumor Progression From Ovarian Endometriotic Cyst to Clear Cell and Endometrioid Carcinoma [J].
Ayhan, Ayse ;
Mao, Tsui-Lien ;
Seckin, Tamer ;
Wu, Chen-Hsuan ;
Guan, Bin ;
Ogawa, Hiroshi ;
Futagami, Masayuki ;
Mizukami, Hiroki ;
Yokoyama, Yoshihito ;
Kurman, Robert J. ;
Shih, Ie-Ming .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2012, 22 (08) :1310-1315
[6]   ARID1A mutation sensitizes most ovarian clear cell carcinomas to BET inhibitors [J].
Berns, Katrien ;
Caumanns, Joseph J. ;
Hijmans, E. Marielle ;
Gennissen, Annemiek M. C. ;
Severson, Tesa M. ;
Evers, Bastiaan ;
Wisman, G. Bea A. ;
Meersma, Gert Jan ;
Lieftink, Cor ;
Beijersbergen, Roderick L. ;
Itamochi, Hiroaki ;
van der Zee, Ate G. J. ;
de Jong, Steven ;
Bernards, Rene .
ONCOGENE, 2018, 37 (33) :4611-4625
[7]   Genome Profiling of Pancreatic Adenocarcinoma [J].
Birnbaum, David J. ;
Adelaide, Jose ;
Mamessier, Emilie ;
Finetti, Pascal ;
Lagarde, Arnaud ;
Monges, Genevieve ;
Viret, Frederic ;
Goncalves, Anthony ;
Turrini, Olivier ;
Delpero, Jean-Robert ;
Iovanna, Juan ;
Giovannini, Marc ;
Birnbaum, Daniel ;
Chaffanet, Max .
GENES CHROMOSOMES & CANCER, 2011, 50 (06) :456-465
[8]   ARID1A-mutated ovarian cancers depend on HDAC6 activity [J].
Bitler, Benjamin G. ;
Wu, Shuai ;
Park, Pyoung Hwa ;
Hai, Yang ;
Aird, Katherine M. ;
Wang, Yemin ;
Zhai, Yali ;
Kossenkov, Andrew V. ;
Vara-Ailor, Ana ;
Rauscher, Frank J., III ;
Zou, Weiping ;
Speicher, David W. ;
Huntsman, David G. ;
Conejo-Garcia, Jose R. ;
Cho, Kathleen R. ;
Christianson, David W. ;
Zhang, Rugang .
NATURE CELL BIOLOGY, 2017, 19 (08) :962-+
[9]   Epigenetic synthetic lethality in ovarian clear cell carcinoma: EZH2 and ARID1A mutations [J].
Bitler, Benjamin G. ;
Aird, Katherine M. ;
Zhang, Rugang .
MOLECULAR & CELLULAR ONCOLOGY, 2016, 3 (01)
[10]   Potential therapeutic targets in ARID1A-mutated cancers [J].
Bitler, Benjamin G. ;
Fatkhutdinov, Nail ;
Zhang, Rugang .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2015, 19 (11) :1419-1422