促红细胞生成素肝细胞(Eph)受体
以法林
EPH受体A2
血管生成
癌症研究
转移
癌变
受体
癌症
信号转导
生物
肿瘤进展
药理学
医学
细胞生物学
受体酪氨酸激酶
生物化学
遗传学
作者
Asmat Ullah,Anam Razzaq,Chuanzan Zhou,Najeeb Ullah,Somia Shehzadi,Tariq Aziz,Mohammad Y. Alfaifi,Serag Eldin I. Elbehairi,Haroon Iqbal
出处
期刊:Current Protein & Peptide Science
[Bentham Science Publishers]
日期:2023-11-01
卷期号:25 (3): 244-255
被引量:10
标识
DOI:10.2174/0113892037269589231017055642
摘要
Eph receptors and their Eph receptor-interacting (ephrin) ligands comprise a vital cell communication system with several functions. In cancer cells, there was evidence of bilateral Eph receptor signaling with both tumor-suppressing and tumor-promoting actions. As a member of the Eph receptor family, EphB4 has been linked to tumor angiogenesis, growth, and metastasis, which makes it a viable and desirable target for drug development in therapeutic applications. Many investigations have been conducted over the last decade to elucidate the structure and function of EphB4 in association with its ligand ephrinB2 for its involvement in tumorigenesis. Although several EphB4-targeting drugs have been investigated, and some selective inhibitors have been evaluated in clinical trials. This article addresses the structure and function of the EphB4 receptor, analyses its possibility as an anticancer therapeutic target, and summarises knowledge of EphB4 kinase inhibitors. To summarise, EphB4 is a difficult but potential treatment option for cancers.
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