Zhao Ruogang, Liu Jianhao, Li Zhaohuan, Zhang Wenhui, Wang Feng, Zhang Bo
School of Pharmacy, Weifang Medical University, Weifang 261053, China.
Pharmaceutics. 2022 Jul 25;14(8):1541. doi: 10.3390/pharmaceutics14081541.
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.
趋化因子可通过与G蛋白偶联受体相互作用诱导细胞趋化迁移,在癌症发展过程中发挥重要的调节作用。CXC趋化因子配体12(CXCL12)可特异性结合CXC趋化因子受体4(CXCR4),并通过多种信号通路与癌症进展密切相关。近年来,许多CXCR4拮抗剂已在临床试验中进行了测试;然而,普乐沙福(AMD3100)是迄今为止唯一已获批上市的药物。在这篇综述中,我们首先总结介导CXCL12/CXCR4轴生理效应的机制。然后,我们描述CXCL12/CXCR4拮抗剂的用途。最后,我们讨论作用于CXCL12/CXCR4生物学轴的纳米药物递送系统的用途。