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Targeting Macrophages: Therapeutic Approaches in Cancer

Overview
Specialty Pharmacology
Date 2018 Oct 27
PMID 30361552
Citations 890
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Abstract

Infiltration of macrophages in solid tumours is associated with poor prognosis and correlates with chemotherapy resistance in most cancers. In mouse models of cancer, macrophages promote cancer initiation and malignant progression by stimulating angiogenesis, increasing tumour cell migration, invasion and intravasation and suppressing antitumour immunity. At metastatic sites, macrophages promote tumour cell extravasation, survival and subsequent growth. Each of these pro-tumoural activities is promoted by a subpopulation of macrophages that express canonical markers but have unique transcriptional profiles, which makes tumour-associated macrophages (TAMs) good targets for anticancer therapy in humans through either their ablation or their re-differentiation away from pro-tumoural towards antitumoural states. In this Review, we evaluate the state of the art of TAM-targeting strategies, focusing on the limitations and potential side effects of the different therapies such as toxicity, rebound effects and compensatory mechanisms. We provide an extensive overview of the different types of therapy used in the clinic and their limitations in light of known macrophage biology and propose new strategies for targeting TAMs.

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References
1.
Morandi F, Pistoia V . Interactions between HLA-G and HLA-E in Physiological and Pathological Conditions. Front Immunol. 2014; 5:394. PMC: 4141331. DOI: 10.3389/fimmu.2014.00394. View

2.
Gao D, Joshi N, Choi H, Ryu S, Hahn M, Catena R . Myeloid progenitor cells in the premetastatic lung promote metastases by inducing mesenchymal to epithelial transition. Cancer Res. 2012; 72(6):1384-94. PMC: 8543151. DOI: 10.1158/0008-5472.CAN-11-2905. View

3.
Sotsios Y, Ward S . Phosphoinositide 3-kinase: a key biochemical signal for cell migration in response to chemokines. Immunol Rev. 2001; 177:217-35. DOI: 10.1034/j.1600-065x.2000.17712.x. View

4.
Bergamaschi A, Tagliabue E, Sorlie T, Naume B, Triulzi T, Orlandi R . Extracellular matrix signature identifies breast cancer subgroups with different clinical outcome. J Pathol. 2007; 214(3):357-67. DOI: 10.1002/path.2278. View

5.
Sharma P, Allison J . Immune checkpoint targeting in cancer therapy: toward combination strategies with curative potential. Cell. 2015; 161(2):205-14. PMC: 5905674. DOI: 10.1016/j.cell.2015.03.030. View