Targeting tumor-associated macrophages as an antitumor strategy

Biochem Pharmacol. 2021 Jan:183:114354. doi: 10.1016/j.bcp.2020.114354. Epub 2020 Dec 3.

Abstract

Tumor-associated macrophages (TAMs) are the most widely infiltrating immune cells in the tumor microenvironment (TME). Clinically, the number of TAMs is closely correlated with poor outcomes in multiple cancers. The biological actions of TAMs are complex and diverse, including mediating angiogenesis, promoting tumor invasion and metastasis, and building an immunosuppressive microenvironment. Given these pivotal roles of TAMs in tumor development, TAM-based strategies are attractive and used in certain tumor therapies, including inhibition of angiogenic signalling, blockade of the immune checkpoint, and macrophage enhancement phagocytosis. Several attempts to develop TAM-targeted agents have been made to deplete TAMs or reprogram the behaviour of TAMs. Some have shown a favourable curative effect in monotherapy, combination with chemotherapy or immunotherapy in clinical trials. Additionally, a new macrophage-based cell therapeutic technology was recently developed by equipping macrophages with CAR molecules. It is expected to break through barriers to solid tumor treatment. Although TAM-related studies have yielded positive antitumor outcomes, further investigations are needed to better characterize TAMs, which will benefit further establishment of novel strategies for tumor therapy. Here, we concisely summarize the functions of TAMs in the TME and comprehensively introduce the latest TAM-based regimens in cancer treatment.

Keywords: Cancer immunotherapy; Combinatory strategies; TAMs; Therapeutic target; Tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Drug Delivery Systems / methods*
  • Drug Delivery Systems / trends
  • Humans
  • Immunosuppressive Agents / administration & dosage
  • Immunotherapy / methods*
  • Immunotherapy / trends
  • Neoplasms / drug therapy
  • Neoplasms / immunology*
  • Receptors, Chimeric Antigen / antagonists & inhibitors
  • Receptors, Chimeric Antigen / immunology
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / immunology*
  • Tumor-Associated Macrophages / drug effects
  • Tumor-Associated Macrophages / immunology*

Substances

  • Antineoplastic Agents
  • Immunosuppressive Agents
  • Receptors, Chimeric Antigen