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Chemokines Modulate Immune Surveillance in Tumorigenesis, Metastasis, and Response to Immunotherapy

Overview
Journal Front Immunol
Date 2019 Mar 16
PMID 30873179
Citations 181
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Abstract

Chemokines are small secreted proteins that orchestrate migration and positioning of immune cells within the tissues. Chemokines are essential for the function of the immune system. Accumulating evidence suggest that chemokines play important roles in tumor microenvironment. In this review we discuss an association of chemokine expression and activity within the tumor microenvironment with cancer outcome. We summarize regulation of immune cell recruitment into the tumor by chemokine-chemokine receptor interactions and describe evidence implicating chemokines in promotion of the "inflamed" immune-cell enriched tumor microenvironment. We review both tumor-promoting function of chemokines, such as regulation of tumor metastasis, and beneficial chemokine roles, including stimulation of anti-tumor immunity and response to immunotherapy. Finally, we discuss the therapeutic strategies target tumor-promoting chemokines or induce/deliver beneficial chemokines within the tumor focusing on pre-clinical studies and clinical trials going forward. The goal of this review is to provide insight into comprehensive role of chemokines and their receptors in tumor pathobiology and treatment.

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References
1.
Hamann A, Syrbe U . T-cell trafficking into sites of inflammation. Rheumatology (Oxford). 2000; 39(7):696-9. DOI: 10.1093/rheumatology/39.7.696. View

2.
Reinhardt R, Khoruts A, Merica R, ZELL T, Jenkins M . Visualizing the generation of memory CD4 T cells in the whole body. Nature. 2001; 410(6824):101-5. DOI: 10.1038/35065111. View

3.
Saji H, Koike M, Yamori T, Saji S, Seiki M, Matsushima K . Significant correlation of monocyte chemoattractant protein-1 expression with neovascularization and progression of breast carcinoma. Cancer. 2001; 92(5):1085-91. DOI: 10.1002/1097-0142(20010901)92:5<1085::aid-cncr1424>3.0.co;2-k. View

4.
Henning G, Ohl L, Junt T, Reiterer P, Brinkmann V, Nakano H . CC chemokine receptor 7-dependent and -independent pathways for lymphocyte homing: modulation by FTY720. J Exp Med. 2001; 194(12):1875-81. PMC: 2193576. DOI: 10.1084/jem.194.12.1875. View

5.
Azenshtein E, Luboshits G, Shina S, Neumark E, Shahbazian D, Weil M . The CC chemokine RANTES in breast carcinoma progression: regulation of expression and potential mechanisms of promalignant activity. Cancer Res. 2002; 62(4):1093-102. View