Divison of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of California, Irvine, Medical Center, 101 The City Drive, Building 56, Room 260, Orange, CA 92868, USA.
Expert Rev Anticancer Ther. 2012 Jan;12(1):51-62. doi: 10.1586/era.11.194.
While the role of Wnt signaling is well established in colorectal carcinogenesis, its function in gynecologic cancers has not been elucidated. Here, we describe the current state of knowledge of canonical Wnt signaling in endometrial cancer (EC), and its implications for future therapeutic targets. Deregulation of the Wnt/β-catenin signaling pathway in EC occurs by inactivating β-catenin mutations in approximately 10-45% of ECs, and via downregulation of Wnt antagonists by epigenetic silencing. The Wnt pathway is intimately involved with estrogen and progesterone, and emerging data implicate it in other important signaling pathways, such as mTOR and Hedgehog. While no therapeutic agents targeting the Wnt signaling pathway are currently in clinical trials, the preclinical data presented suggest a role for Wnt signaling in uterine carcinogenesis, with further research warranted to elucidate the mechanism of action and to proceed towards targeted cancer drug development.
尽管 Wnt 信号通路在结直肠癌的发生中作用已得到充分证实,但它在妇科癌症中的功能尚未阐明。在这里,我们描述了经典 Wnt 信号通路在子宫内膜癌 (EC) 中的当前研究现状,及其对未来治疗靶点的意义。Wnt/β-连环蛋白信号通路在 EC 中的失调是通过大约 10-45%的 EC 中β-连环蛋白突变失活,以及通过表观遗传沉默下调 Wnt 拮抗剂来实现的。Wnt 通路与雌激素和孕激素密切相关,新出现的数据表明它与其他重要的信号通路(如 mTOR 和 Hedgehog)有关。虽然目前没有针对 Wnt 信号通路的治疗药物在临床试验中,但提出的临床前数据表明 Wnt 信号在子宫癌发生中起作用,需要进一步研究以阐明其作用机制,并朝着靶向癌症药物开发的方向前进。