Department of Biochemistry and Medical Chemistry, Pomeranian Medical University in Szczecin, Powstańców Wlkp. 72 Av., 70-111 Szczecin, Poland.
Clinic of Cardiology, Pomeranian Medical University in Szczecin, Powstańców Wlkp. 72 Av., 70-111 Szczecin, Poland.
Int J Mol Sci. 2022 Feb 16;23(4):2168. doi: 10.3390/ijms23042168.
Chemokines are a group of about 50 chemotactic cytokines crucial for the migration of immune system cells and tumor cells, as well as for metastasis. One of the 20 chemokine receptors identified to date is CXCR2, a G-protein-coupled receptor (GPCR) whose most known ligands are CXCL8 (IL-8) and CXCL1 (GRO-α). In this article we present a comprehensive review of literature concerning the role of CXCR2 in cancer. We start with regulation of its expression at the transcriptional level and how this regulation involves microRNAs. We show the mechanism of CXCR2 signal transduction, in particular the action of heterotrimeric G proteins, phosphorylation, internalization, intracellular trafficking, sequestration, recycling, and degradation of CXCR2. We discuss in detail the mechanism of the effects of activated CXCR2 on the actin cytoskeleton. Finally, we describe the involvement of CXCR2 in cancer. We focused on the importance of CXCR2 in tumor processes such as proliferation, migration, and invasion of tumor cells as well as the effects of CXCR2 activation on angiogenesis, lymphangiogenesis, and cellular senescence. We also discuss the importance of CXCR2 in cell recruitment to the tumor niche including tumor-associated neutrophils (TAN), tumor-associated macrophages (TAM), myeloid-derived suppressor cells (MDSC), and regulatory T (T) cells.
趋化因子是一组约 50 种趋化细胞因子,对于免疫系统细胞和肿瘤细胞的迁移以及转移至关重要。迄今为止,已鉴定出 20 种趋化因子受体之一是 CXCR2,它是一种 G 蛋白偶联受体(GPCR),其最著名的配体是 CXCL8(IL-8)和 CXCL1(GRO-α)。在本文中,我们全面回顾了有关 CXCR2 在癌症中的作用的文献。我们从其在转录水平的表达调控开始,以及这种调控如何涉及 microRNAs。我们展示了 CXCR2 信号转导的机制,特别是异三聚体 G 蛋白、磷酸化、内化、细胞内运输、隔离、回收和 CXCR2 降解的作用。我们详细讨论了激活的 CXCR2 对肌动蛋白细胞骨架的影响的机制。最后,我们描述了 CXCR2 与癌症的关系。我们重点介绍了 CXCR2 在肿瘤过程中的重要性,如肿瘤细胞的增殖、迁移和侵袭,以及 CXCR2 激活对血管生成、淋巴管生成和细胞衰老的影响。我们还讨论了 CXCR2 在细胞募集到肿瘤微环境中的重要性,包括肿瘤相关中性粒细胞(TAN)、肿瘤相关巨噬细胞(TAM)、髓系来源的抑制细胞(MDSC)和调节性 T(T)细胞。