促红细胞生成素肝细胞(Eph)受体
受体酪氨酸激酶
以法林
EPH受体A2
癌症研究
酪氨酸激酶
转移
信号转导
生物
癌变
靶向治疗
ROR1型
癌症
细胞生物学
受体
血管生成
受体蛋白酪氨酸激酶
血小板源性生长因子受体
生物化学
生长因子
遗传学
作者
Yinnan Chen,Hongmei Zhang,Yanmin Zhang
标识
DOI:10.1016/j.semcancer.2017.10.002
摘要
Eph receptors and their Eph receptor-interacting (ephrin) ligands together form an important cell communication system with diverse roles. Experimental evidence demonstrated Eph receptor bidirectional signaling with both tumor-suppressing and tumor-promoting activities in cancer cells. The tyrosine kinase EphB4, a member of the Eph receptor family, has been associated with tumor angiogenesis, growth and metastasis, thus making it a valuable and attractive target for drug design for therapeutic applications. In the past decade, many studies have focused on elucidating the structure and function of EphB4 in complex with its ligand ephrinB2 for their role in carcinogenesis. Meanwhile, an array of compounds targeting EphB4 have been studied and several selective inhibitors have been tested in clinical studies. This review discusses the structure and function of the EphB4 receptor, analyzes its potential as a target for anticancer therapy, and summarizes the information about inhibitors of EphB4 kinase activity. Conclusively, EphB4 is a challenging but promising therapeutic target in cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI