趋化因子受体
CXCR4型
CXCR4拮抗剂
普乐沙福
趋化因子受体
趋化因子
药物输送
药品
药理学
医学
癌症
趋化性
受体
生物信息学
计算生物学
生物
癌症研究
化学
内科学
有机化学
作者
Ruogang Zhao,Jianhao Liu,Zhaohuan Li,Wenhui Zhang,Feng Wang,Bo Zhang
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2022-07-25
卷期号:14 (8): 1541-1541
被引量:19
标识
DOI:10.3390/pharmaceutics14081541
摘要
Chemokines can induce chemotactic cell migration by interacting with G protein-coupled receptors to play a significant regulatory role in the development of cancer. CXC chemokine-12 (CXCL12) can specifically bind to CXC chemokine receptor 4 (CXCR4) and is closely associated with the progression of cancer via multiple signaling pathways. Over recent years, many CXCR4 antagonists have been tested in clinical trials; however, Plerixafor (AMD3100) is the only drug that has been approved for marketing thus far. In this review, we first summarize the mechanisms that mediate the physiological effects of the CXCL12/CXCR4 axis. Then, we describe the use of CXCL12/CXCR4 antagonists. Finally, we discuss the use of nano-based drug delivery systems that exert action on the CXCL12/CXCR4 biological axis.
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