Department of Gynecology and Obstetrics, Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto, Japan.
Int J Clin Oncol. 2009 Oct;14(5):383-91. doi: 10.1007/s10147-009-0935-y. Epub 2009 Oct 25.
Recent molecular and pathological evidence suggests that endometriosis is a monoclonal, neoplastic disease. Moreover, endometriosis serves as a precursor of ovarian cancer (endometriosis-associated ovarian cancer; EAOC), especially of the endometrioid and clear cell subtypes. Although a variety of molecular events, such as p53 alteration, PTEN silencing, K-ras mutations, and HNF-1 activation, have been identified in EAOC, its precise carcinogenic mechanism remains poorly understood. Our recent data indicate that microenvironmental factors, including oxidative stress and inflammation, play an important role in the carcinogenesis and phenotype of EAOC. The management of endometriosis from the standpoint of EAOC is not standardized yet. To this end, clarification of the precise natural course and the risk factors that contribute to malignant transformation remain important goals. Among the phenotypes of EAOC, clear cell carcinoma, seems to require a specific treatment strategy, including molecular targeting.
最近的分子和病理学证据表明,子宫内膜异位症是一种单克隆、肿瘤性疾病。此外,子宫内膜异位症是卵巢癌(与子宫内膜异位症相关的卵巢癌;EAOC)的前身,尤其是子宫内膜样和透明细胞亚型。尽管在 EAOC 中已经确定了多种分子事件,如 p53 改变、PTEN 沉默、K-ras 突变和 HNF-1 激活,但它的确切致癌机制仍不清楚。我们最近的数据表明,微环境因素,包括氧化应激和炎症,在 EAOC 的发生和表型中发挥重要作用。从 EAOC 的角度来看,子宫内膜异位症的管理尚未标准化。为此,阐明导致恶性转化的精确自然病程和危险因素仍然是重要目标。在 EAOC 的表型中,透明细胞癌似乎需要特定的治疗策略,包括分子靶向治疗。