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CXC 趋化因子受体 4(CXCR4)在癌症治疗中的阻断作用。

CXC chemokine receptor 4 (CXCR4) blockade in cancer treatment.

机构信息

The First Clinical Medical College, Xuzhou Medical University, 221000, Xuzhou, China.

Infectious Diseases and Tropical Medicine Research Center (IDTMRC), Department of Aerospace and Subaquatic Medicine, AJA University of Medicinal Sciences, Tehran, Iran.

出版信息

J Cancer Res Clin Oncol. 2023 Aug;149(10):7945-7968. doi: 10.1007/s00432-022-04444-w. Epub 2023 Mar 11.

Abstract

CXC chemokine receptor type 4 (CXCR4) is a member of the G protein-coupled receptors (GPCRs) superfamily and is specific for CXC chemokine ligand 12 (CXCL12, also known as SDF-1), which makes CXCL12/CXCR4 axis. CXCR4 interacts with its ligand, triggering downstream signaling pathways that influence cell proliferation chemotaxis, migration, and gene expression. The interaction also regulates physiological processes, including hematopoiesis, organogenesis, and tissue repair. Multiple evidence revealed that CXCL12/CXCR4 axis is implicated in several pathways involved in carcinogenesis and plays a key role in tumor growth, survival, angiogenesis, metastasis, and therapeutic resistance. Several CXCR4-targeting compounds have been discovered and used for preclinical and clinical cancer therapy, most of which have shown promising anti-tumor activity. In this review, we summarized the physiological signaling of the CXCL12/CXCR4 axis and described the role of this axis in tumor progression, and focused on the potential therapeutic options and strategies to block CXCR4.

摘要

CXC 趋化因子受体 4(CXCR4)是 G 蛋白偶联受体(GPCRs)超家族的成员,特异性识别 CXC 趋化因子配体 12(也称为 SDF-1),形成 CXCL12/CXCR4 轴。CXCR4 与其配体相互作用,触发下游信号通路,影响细胞增殖、趋化性、迁移和基因表达。这种相互作用还调节生理过程,包括造血、器官发生和组织修复。多项证据表明,CXCL12/CXCR4 轴参与了癌症发生的多个途径,并在肿瘤生长、存活、血管生成、转移和治疗耐药性中发挥关键作用。已经发现并使用了几种靶向 CXCR4 的化合物进行临床前和临床癌症治疗,其中大多数显示出有希望的抗肿瘤活性。在这篇综述中,我们总结了 CXCL12/CXCR4 轴的生理信号,并描述了该轴在肿瘤进展中的作用,重点介绍了阻断 CXCR4 的潜在治疗选择和策略。

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