Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Onco Targets Ther. 2014 Sep 23;7:1647-52. doi: 10.2147/OTT.S49993. eCollection 2014.
Clear cell adenocarcinoma (CCC) of the ovary accounts for 10% of epithelial ovarian cancer and is a distinct entity from other epithelial ovarian carcinomas. It arises from the endometriosis. CCC has specific biological and clinical behavior. Compared with other histological types, CCC shows a chemoresistant phenotype, which leads to poorer prognosis. Thus, development of new target-based therapies remains an unmet need for these patients. Mutations in the gene ARID1A have been found to occur in high frequency in CCC. The majority of these mutations lead to a loss of expression of the ARID1A protein, which is a subunit of the SWItch/Sucrose NonFermentable (SWI/SNF) chromatin remodeling complex and considered as a bona fide tumor suppressor. Upregulation of the PIK3/AKT/mTOR pathway, particularly through mutations of PIK3CA and inactivation of PTEN, is involved in tumorigenesis of CCC. Targeting angiogenesis, the Met protooncogene pathway, and HER2 are also discussed in this review.
卵巢透明细胞癌(CCC)约占上皮性卵巢癌的 10%,是一种与其他上皮性卵巢癌不同的实体瘤。它起源于子宫内膜异位症。CCC 具有特定的生物学和临床行为。与其他组织学类型相比,CCC 表现出化学抗性表型,导致预后较差。因此,为这些患者开发新的基于靶点的治疗方法仍然是未满足的需求。已经发现 ARID1A 基因的突变在 CCC 中高频发生。这些突变中的大多数导致 ARID1A 蛋白的表达丧失,ARID1A 蛋白是 SWItch/Sucrose NonFermentable(SWI/SNF)染色质重塑复合物的一个亚单位,被认为是一种真正的肿瘤抑制因子。PIK3/AKT/mTOR 通路的上调,特别是通过 PIK3CA 的突变和 PTEN 的失活,参与了 CCC 的肿瘤发生。本文还讨论了针对血管生成、Met 原癌基因通路和 HER2 的治疗方法。