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趋化因子:肿瘤微环境中虽不起眼却强大的参与者。

Chemokines: humble yet mighty players in the tumour microenvironment.

作者信息

Xavier Hima, Gireesh Athira Gireesh Moly, Thomas Juvin Ann, Suboj Priya, Suresh Arya, Biju Emmanuel, Baby Arya, Dominic Roshin Thomas, Babykutty Suboj

机构信息

Centre for Tumour Immunology and Microenvironment, Department of Zoology, Mar Ivanios College, Thiruvananthapuram, Kerala, India.

Department of Biotechnology, CEPCI Laboratory and Research Institute, Kollam, India.

出版信息

Front Immunol. 2025 Aug 7;16:1601756. doi: 10.3389/fimmu.2025.1601756. eCollection 2025.


DOI:10.3389/fimmu.2025.1601756
PMID:40852716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12367674/
Abstract

Chemokines are tiny chemotactic cytokines which play a crucial role in pathophysiology by maintaining homeostasis and inflammation. Their role in the tumour microenvironment is very much puzzling because of both pro- and anti-tumourigenic effects. Chemokines have gained much attention today, since it has been recognized that they are game changers in the TME via controlling immune cell recruitment, angiogenesis, metastasis, tumour growth and drug resistance. In this review, we are exploring the role of several chemokines and their receptors in the TME with special focus on immune cell recruitment, immune surveillance, regulation of immune checkpoints and epithelial mesenchymal transition. We are also reviewing the possibility of targeting chemokines along with immunotherapy for better outcome and disease-free survival. A better understanding on the dual role of chemokine in the TME might help to implement novel therapeutic interventions and adopt precision in targeted therapy.

摘要

趋化因子是微小的趋化性细胞因子,通过维持体内平衡和炎症在病理生理学中发挥关键作用。由于其具有促肿瘤和抗肿瘤生成的双重作用,它们在肿瘤微环境中的作用非常令人困惑。如今,趋化因子已备受关注,因为人们认识到它们通过控制免疫细胞募集、血管生成、转移、肿瘤生长和耐药性,成为肿瘤微环境中的关键因素。在本综述中,我们探讨了几种趋化因子及其受体在肿瘤微环境中的作用,特别关注免疫细胞募集、免疫监视、免疫检查点调节和上皮间质转化。我们还回顾了将趋化因子与免疫疗法联合靶向治疗以获得更好疗效和无病生存期的可能性。更好地理解趋化因子在肿瘤微环境中的双重作用可能有助于实施新的治疗干预措施并实现靶向治疗的精准性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/fe91f98f1fd4/fimmu-16-1601756-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/a2b553fbcb8e/fimmu-16-1601756-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/a4973b28d4cb/fimmu-16-1601756-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/fe91f98f1fd4/fimmu-16-1601756-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/a2b553fbcb8e/fimmu-16-1601756-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/a4973b28d4cb/fimmu-16-1601756-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/12367674/fe91f98f1fd4/fimmu-16-1601756-g003.jpg

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本文引用的文献

[1]
CXCL2: a key player in the tumor microenvironment and inflammatory diseases.

Cancer Cell Int. 2025-4-7

[2]
Overcoming immunotherapy resistance in hepatocellular carcinoma by targeting myeloid IL-8/CXCR2 signaling.

Mol Ther. 2025-4-2

[3]
The multifaceted role of XCL1 in health and disease.

Protein Sci. 2025-2

[4]
Estimate the relationship between CXCR4-SDF-1 axis and inhibitory molecules (CTLA4 and PD-1) in patients with colon cancer.

Narra J. 2024-12

[5]
Harnessing the tumor microenvironment: targeted cancer therapies through modulation of epithelial-mesenchymal transition.

J Hematol Oncol. 2025-1-13

[6]
Anti-CTLA-4 generates greater memory response than anti-PD-1 via TCF-1.

Proc Natl Acad Sci U S A. 2025-1-14

[7]
Immune checkpoint blockade in experimental bacterial infections.

J Infect. 2025-2

[8]
CCR5 and IL-12 co-expression in CAR T cells improves antitumor efficacy by reprogramming tumor microenvironment in solid tumors.

Cancer Immunol Immunother. 2025-1-3

[9]
Unveiling the nexus: The tumor microenvironment as a strategic frontier in viral cancers.

Cytokine. 2025-1

[10]
Characteristics of a CCL21 Gene-Modified Dendritic Cell Vaccine Utilized for a Clinical Trial in Non-Small Cell Lung Cancer.

Mol Cancer Ther. 2025-2-4

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