Samartzis Eleftherios P, Labidi-Galy S Intidhar, Moschetta Michele, Uccello Mario, Kalaitzopoulos Dimitrios R, Perez-Fidalgo J Alejandro, Boussios Stergios
Department of Gynecology and Gynecological Cancer Center, University Hospital Zurich, Zurich, Switzerland.
Department of Oncology, Hôpitaux Universitaires de Genève, Geneva, Switzerland.
Ann Transl Med. 2020 Dec;8(24):1712. doi: 10.21037/atm-20-3022a.
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 oligo- or 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 () 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 endometriosis-associated ovarian cancer, the occurrence in a relatively young population, and the high proportion of platinum-resistant 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.
子宫内膜异位症是一种良性妇科疾病,影响着高达十分之一的育龄女性。它的定义是在子宫腔外的部位存在类似子宫内膜的组织。它常引起慢性疼痛等症状,最常见的是与月经周期相关的疼痛以及不孕,但也可能症状轻微或无症状。有证据表明,某些卵巢癌(OC)组织学类型,主要是卵巢透明细胞癌(OCCC)和子宫内膜样癌(EnOC),可能起源于子宫内膜异位症。这些癌症中最常见的基因组改变是富含AT的相互作用结构域包含蛋白1A(ARID1A)基因的突变,ARID1A是SWI/SNF染色质重塑复合物的一个亚基,以及磷脂酰肌醇3激酶(PI3K)/AKT/雷帕霉素靶蛋白(mTOR)途径的改变,这些改变经常同时发生。在ARID1A缺陷的癌症中,临床前实验数据表明存在不同的可靶向机制,包括表观遗传调控、细胞周期、基因组不稳定、PI3K/AKT/mTOR途径、炎症途径、免疫调节或代谢改变,作为潜在的精准肿瘤学方法。这些策略大多基于合成致死的概念,即ARID1A缺陷的肿瘤对不同化合物更敏感。其中一些方法目前正在早期临床试验中进行研究或最近已在早期临床试验中进行了研究。这些突变在子宫内膜异位症相关卵巢癌中显著频繁出现、在相对年轻人群中出现以及铂耐药疾病的高比例,无疑值得进一步研究该人群的精准肿瘤学机会。此外,关于子宫内膜异位症相关卵巢癌中致癌突变的深入了解可能对早期癌症检测有潜在帮助。然而,正如最近的研究所表明的,由于良性子宫内膜异位组织中体细胞突变的频繁发生,这种方法可能会变得复杂。在对当前文献的这篇叙述性综述中,我们将讨论关于子宫内膜异位症相关卵巢癌的现有数据,特别强调流行病学、诊断以及可能对未来治疗有影响和临床适用性的分子变化。