Literature DB >> 20635976

Tumor-associated macrophages as targets for tumor immunotherapy.

Andreas Weigert1, Divya Sekar, Bernhard Brüne.   

Abstract

Restoration of one of the major physiological functions of the body's immune response, the rejection of malignant cells, is a promising yet challenging task for cancer therapy. Prinicipally, immunotherapeutic approaches make use of cells of the adaptive immune system, since antigen-based tumor rejection might be the most specific approach. However, other immune cell populations, such as tumor-associated macrophages (TAMs), contribute significantly to protumor mechanisms elicited by a distorted immune response. In this review, we summarize the current knowledge about the pathology of TAMs and discuss potential therapeutic approaches to overcome TAM-mediated tumor promotion. Hereby, we focus on TAM phenotypes that were observed in the clinically relevant stages of cancer progression. The function of macrophages and other inflammatory cells in the onset of cancer has been discussed elsewhere.

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Year:  2009        PMID: 20635976     DOI: 10.2217/1750743X.1.1.83

Source DB:  PubMed          Journal:  Immunotherapy        ISSN: 1750-743X            Impact factor:   4.196


  15 in total

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Review 4.  Anti-tumour strategies aiming to target tumour-associated macrophages.

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Journal:  Immunology       Date:  2013-02       Impact factor: 7.397

Review 5.  Targeting tumor-infiltrating macrophages to combat cancer.

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Journal:  Immunotherapy       Date:  2013-10       Impact factor: 4.196

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7.  GATA3 expression correlates with poor prognosis and tumor-associated macrophage infiltration in peripheral T cell lymphoma.

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Journal:  Oncotarget       Date:  2016-10-04

Review 8.  Gold nanoparticle mediated cancer immunotherapy.

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9.  Erlotinib augmentation with dapsone for rash mitigation and increased anti-cancer effectiveness.

Authors:  R E Kast
Journal:  Springerplus       Date:  2015-10-23

Review 10.  Targeting tumor-associated macrophages to combat pancreatic cancer.

Authors:  Ran Cui; Wen Yue; Edmund C Lattime; Mark N Stein; Qing Xu; Xiang-Lin Tan
Journal:  Oncotarget       Date:  2016-08-02
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