血管内皮生长因子
医学
血管生成
药理学
药物开发
血液学
癌症研究
酪氨酸激酶
生物信息学
受体
血管内皮生长因子受体
药品
内科学
生物
作者
Yun Liu,Yang Li,Yuxi Wang,Caiyu Lin,Dan Zhang,Jun-Cheng Chen,Liang Ouyang,Fengbo Wu,Jifa Zhang,Lei Chen
标识
DOI:10.1186/s13045-022-01310-7
摘要
Abstract Vascular endothelial growth factor receptors (VEGFRs) are a family of receptor protein tyrosine kinases that play an important role in the regulation of tumor-induced angiogenesis. Currently, VEGFR inhibitors have been widely used in the treatment of various tumors. However, current VEGFR inhibitors are limited to a certain extent due to limited clinical efficacy and potential toxicity, which hinder their clinical application. Thus, the development of new strategies to improve the clinical outcomes and minimize the toxic effects of VEGFR inhibitors is required. Given the synergistic effect of VEGFR and other therapies in tumor development and progression, VEGFR dual-target inhibitors are becoming an attractive approach due to their favorable pharmacodynamics, low toxicity, and anti-resistant effects. This perspective provides an overview of the development of VEGFR dual-target inhibitors from multiple aspects, including rational target combinations, drug discovery strategies, structure–activity relationships and future directions.
科研通智能强力驱动
Strongly Powered by AbleSci AI