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肿瘤微环境中的 CXCL5/CXCR2 轴作为潜在的诊断生物标志物和治疗靶点。

CXCL5/CXCR2 axis in tumor microenvironment as potential diagnostic biomarker and therapeutic target.

机构信息

Medical Center for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210011, Jiangsu, P. R. China.

Department of Surgery, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210011, Jiangsu, P. R. China.

出版信息

Cancer Commun (Lond). 2020 Mar;40(2-3):69-80. doi: 10.1002/cac2.12010.

Abstract

The components of the tumor microenvironment (TME) in solid tumors, especially chemokines, are currently attracting much attention from scientists. C-X-C motif chemokine ligand 5 (CXCL5) is one of the important chemokines in TME. Overexpression of CXCL5 is closely related to the survival time, recurrence and metastasis of cancer patients. In TME, CXCL5 binds to its receptors, such as C-X-C motif chemokine receptor 2 (CXCR2), to participate in the recruitment of immune cells and promote angiogenesis, tumor growth, and metastasis. The CXCL5/CXCR2 axis can act as a bridge between tumor cells and host cells in TME. Blocking the transmission of CXCL5/CXCR2 signals can increase the sensitivity and effectiveness of immunotherapy and slow down tumor progression. CXCL5 and CXCR2 are also regarded as biomarkers for predicting prognosis and molecular targets for customizing the treatment. In this review, we summarized the current literature regarding the biological functions and clinical significance of CXCL5/CXCR2 axis in TME. The possibility to use CXCL5 and CXCR2 as potential prognostic biomarkers and therapeutic targets in cancer is also discussed.

摘要

肿瘤微环境(TME)中的成分,尤其是趋化因子,目前引起了科学家们的广泛关注。C-X-C 基序趋化因子配体 5(CXCL5)是 TME 中重要的趋化因子之一。CXCL5 的过表达与癌症患者的生存时间、复发和转移密切相关。在 TME 中,CXCL5 与其受体(如 C-X-C 基序趋化因子受体 2(CXCR2))结合,参与招募免疫细胞,并促进血管生成、肿瘤生长和转移。CXCL5/CXCR2 轴可作为 TME 中肿瘤细胞和宿主细胞之间的桥梁。阻断 CXCL5/CXCR2 信号的传递可以提高免疫治疗的敏感性和有效性,减缓肿瘤的进展。CXCL5 和 CXCR2 也被认为是预测预后的生物标志物和制定治疗方案的分子靶点。本综述总结了目前关于 CXCL5/CXCR2 轴在 TME 中的生物学功能和临床意义的文献。还讨论了将 CXCL5 和 CXCR2 用作癌症潜在预后生物标志物和治疗靶点的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f161/7163794/09e2a931a5af/CAC2-40-69-g001.jpg

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