Department of Endocrinology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, 226014, India.
Division of Endocrinology and CSIR-Central Drug Research Institute, Sitapur Road, Lucknow, 226 031, India.
Semin Cancer Biol. 2022 Nov;86(Pt 3):1105-1121. doi: 10.1016/j.semcancer.2021.12.011. Epub 2022 Jan 1.
Chemokines are small secretory chemotactic cytokines that control the directed migration of immune cells. Chemokines are involved in both anti-and pro-tumorigenic immune responses. Accumulating evidence suggests that the balance between these responses is influenced by several factors such as the stage of tumorigenesis, immune cell activation, recruitment of immune activating or immunosuppressive cells in the tumor microenvironment (TME), and chemokine receptor expression on effector and regulatory target cells. Cancer cells engage in a complex network with their TME components via several factors including growth factors, cytokines and chemokines that are critical for the growth of primary tumor and metastasis. However, chemokines show a multifaceted role in tumor progression including maintenance of stem-like properties, tumor cell proliferation/survival/senescence, angiogenesis, and metastasis. The heterogeneity of solid tumors in primary and metastatic cancers presents a challenge to the development of successful cancer therapy. Despite extensive research on how solid tumors escape immune cell-mediated anti-tumor response, finding an effective therapy for metastatic cancer still remains a challenge. This review discusses the multifarious roles of chemokines in solid tumors including various chemokine signaling pathways such as CXCL8-CXCR1/2, CXCL9, 10, 11-CXCR3, CXCR4-CXCL12, CCL(X)-CCR(X) in primary and metastatic cancers. We further discuss the novel therapeutic approaches that have been developed by major breakthroughs in chemokine research to treat cancer patients by the strategic blockade/activation of these signaling axes alone or in combination with immunotherapies.
趋化因子是一类小的分泌型趋化细胞因子,可控制免疫细胞的定向迁移。趋化因子参与抗肿瘤和促肿瘤免疫反应。越来越多的证据表明,这些反应之间的平衡受到多种因素的影响,如肿瘤发生的阶段、免疫细胞的激活、肿瘤微环境(TME)中免疫激活或免疫抑制细胞的募集,以及效应细胞和调节性靶细胞上的趋化因子受体表达。癌细胞通过多种因素与 TME 成分发生复杂的相互作用,包括生长因子、细胞因子和趋化因子,这些因素对于原发性肿瘤和转移的生长至关重要。然而,趋化因子在肿瘤进展中具有多方面的作用,包括维持干细胞样特性、肿瘤细胞增殖/存活/衰老、血管生成和转移。原发性和转移性癌症中实体瘤的异质性给成功的癌症治疗的发展带来了挑战。尽管对实体瘤如何逃避免疫细胞介导的抗肿瘤反应进行了广泛的研究,但找到转移性癌症的有效治疗方法仍然是一个挑战。本综述讨论了趋化因子在实体瘤中的多种作用,包括各种趋化因子信号通路,如 CXCL8-CXCR1/2、CXCL9、10、11-CXCR3、CXCR4-CXCL12、CCL(X)-CCR(X)在原发性和转移性癌症中的作用。我们进一步讨论了趋化因子研究的重大突破所带来的新型治疗方法,通过单独或联合免疫疗法来靶向这些信号轴的激活或阻断来治疗癌症患者。