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Tumor-Associated Macrophages: Recent Insights and Therapies.

作者信息

Zhou Jiawei, Tang Ziwei, Gao Siyang, Li Chunyu, Feng Yiting, Zhou Xikun

机构信息

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu, China.

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China College of Stomatology, Chinese Academy of Medical Sciences Research Unit of Oral Carcinogenesis and Management, Sichuan University, Chengdu, China.

出版信息

Front Oncol. 2020 Feb 25;10:188. doi: 10.3389/fonc.2020.00188. eCollection 2020.


DOI:10.3389/fonc.2020.00188
PMID:32161718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7052362/
Abstract

Macrophages, which have functions of engulfing and digesting foreign substances, can clear away harmful matter, including cellular debris and tumor cells. Based on the condition of the internal environment, circulating monocytes give rise to mature macrophages, and when they are recruited into the tumor microenvironment and in suitable conditions, they are converted into tumor-associated macrophages (TAMs). Generally, macrophages grow into two main groups called classically activated macrophages (M1) and alternatively activated macrophages (M2). M2 and a small fraction of M1 cells, also known as TAMs, not only lack the function of phagocytizing tumor cells but also help these tumor cells escape from being killed and help them spread to other tissues and organs. In this review, we introduce several mechanisms by which macrophages play a role in the immune regulation of tumor cells, including both killing factors and promoting effects. Furthermore, the targeted therapy for treating tumors based on macrophages is also referred to in our review. We confirm that further studies of macrophage-focused therapeutic strategies and their use in clinical practice are needed to verify their superior efficacy and potential in cancer treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/1045e1d162ec/fonc-10-00188-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/df813bcc48e4/fonc-10-00188-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/185b28d496b4/fonc-10-00188-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/1045e1d162ec/fonc-10-00188-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/df813bcc48e4/fonc-10-00188-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/185b28d496b4/fonc-10-00188-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0d/7052362/1045e1d162ec/fonc-10-00188-g0003.jpg

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本文引用的文献

[1]
GCN2 drives macrophage and MDSC function and immunosuppression in the tumor microenvironment.

Sci Immunol. 2019-12-13

[2]
CSF1R- and SHP2-Inhibitor-Loaded Nanoparticles Enhance Cytotoxic Activity and Phagocytosis in Tumor-Associated Macrophages.

Adv Mater. 2019-10-29

[3]
CD24 signalling through macrophage Siglec-10 is a target for cancer immunotherapy.

Nature. 2019-7-31

[4]
DFMO and 5-Azacytidine Increase M1 Macrophages in the Tumor Microenvironment of Murine Ovarian Cancer.

Cancer Res. 2019-5-14

[5]
Targeting Tyro3, Axl and MerTK (TAM receptors): implications for macrophages in the tumor microenvironment.

Mol Cancer. 2019-5-14

[6]
Potential Diagnostic and Prognostic Role of Microenvironment in Malignant Pleural Mesothelioma.

J Thorac Oncol. 2019-5-9

[7]
Inflammatory Breast Cancer Promotes Development of M2 Tumor-Associated Macrophages and Cancer Mesenchymal Cells through a Complex Chemokine Network.

Cancer Res. 2019-5-1

[8]
IL-10 Family Cytokines IL-10 and IL-22: from Basic Science to Clinical Translation.

Immunity. 2019-4-16

[9]
Glutaminyl cyclase is an enzymatic modifier of the CD47- SIRPα axis and a target for cancer immunotherapy.

Nat Med. 2019-3-4

[10]
Monocyte heterogeneity and functions in cancer.

J Leukoc Biol. 2019-2-18

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