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CXCL12/CXCR4拮抗剂与基于纳米的癌症治疗药物递送系统的最新进展

Recent Advances in CXCL12/CXCR4 Antagonists and Nano-Based Drug Delivery Systems for Cancer Therapy.

作者信息

Zhao Ruogang, Liu Jianhao, Li Zhaohuan, Zhang Wenhui, Wang Feng, Zhang Bo

机构信息

School of Pharmacy, Weifang Medical University, Weifang 261053, China.

出版信息

Pharmaceutics. 2022 Jul 25;14(8):1541. doi: 10.3390/pharmaceutics14081541.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c96/9332179/cb312814d586/pharmaceutics-14-01541-g001.jpg

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