Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Dec;1874(2):188434.
doi: 10.1016/j.bbcan.2020.188434. Epub 2020 Sep 18.

Targeting tumor-associated macrophages for cancer immunotherapy

Affiliations
Review

Targeting tumor-associated macrophages for cancer immunotherapy

Yongheng Shu et al. Biochim Biophys Acta Rev Cancer. 2020 Dec.

Abstract

Macrophages are important effector cells of the innate immune system and are also major components of the tumor microenvironment (TME). Macrophages that are abundant in the TME are called tumor-associated macrophages (TAMs). As TAMs promote strong tumor angiogenesis and support tumor cell survival, they are closely related to tumor growth. Several studies have demonstrated that reducing the density or effects of TAMs can inhibit the growth of tumors, making them targets for cancer immunotherapy, which has become a research hot spot. Several clinical and preclinical trials have studied drugs that inhibit the effects of and reduce the population of phagocytes that target TAMs achieve cancer immunotherapy. In this paper, we summarize the various methods of targeting TAMs for tumor immunotherapy, focusing on TAM mechanisms, sources, and polarization.

Keywords: Immunotherapy; Tumor; Tumor-associated macrophages (TAMs).

PubMed Disclaimer

Publication types

MeSH terms

Substances

LinkOut - more resources