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Tumor-associated macrophages: implications in cancer immunotherapy.

作者信息

Petty Amy J, Yang Yiping

机构信息

Division of Hematologic Malignancies & Cellular Therapy, Department of Medicine, Duke University Medical Center, Box 103005, Durham, NC 27710, USA.

Department of Immunology, Duke University, Durham, NC 27710, USA.

出版信息

Immunotherapy. 2017 Mar;9(3):289-302. doi: 10.2217/imt-2016-0135.


DOI:10.2217/imt-2016-0135
PMID:28231720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5619052/
Abstract

Tumor-associated macrophages (TAMs), representing most of the leukocyte population in solid tumors, demonstrate great phenotypic heterogeneity and diverse functional capabilities under the influence of the local tumor microenvironment. These anti-inflammatory and protumorigenic macrophages modulate the local microenvironment to facilitate tumor growth and metastasis. In this review, we examine the origin of TAMs and the complex regulatory networks within the tumor microenvironment that facilitate the polarization of TAMs toward a protumoral phenotype. More extensively, we evaluate the mechanisms by which TAMs mediate angiogenesis, metastasis, chemotherapeutic resistance and immune evasion. Lastly, we will highlight novel interventional strategies targeting TAMs in preclinical studies and in early clinical trials that have significant potential in improving efficacy of current chemotherapeutic and/or immunotherapeutic approaches.

摘要

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本文引用的文献

[1]
CCL2 Produced by the Glioma Microenvironment Is Essential for the Recruitment of Regulatory T Cells and Myeloid-Derived Suppressor Cells.

Cancer Res. 2016-10-1

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J Leukoc Biol. 2017-1

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[10]
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J Clin Invest. 2015-9

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