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
. 2013 Sep;35(5):585-600.
doi: 10.1007/s00281-013-0367-7. Epub 2013 May 9.

Tumor-associated macrophages: functional diversity, clinical significance, and open questions

Affiliations
Review

Tumor-associated macrophages: functional diversity, clinical significance, and open questions

Subhra K Biswas et al. Semin Immunopathol. 2013 Sep.

Abstract

Inflammation is now a well-recognized hallmark of cancer progression. Tumor-associated macrophages (TAMs) are one of the major inflammatory cells that infiltrate murine and human tumors. While epidemiological studies indicate a clear correlation between TAM density and poor prognosis in a number of human cancers, transgenic studies and transcriptome profiling of TAMs in mice have established their crucial role in cancer progression. In fact, TAMs affect diverse aspects of cancer progression including tumor cell growth and survival, invasion, metastasis, angiogenesis, inflammation, and immunoregulation. New evidences have extended the repertoire of these cells to other tumor promoting activities like interactions with cancer stem cells, response to chemotherapy, and tumor relapse. These findings have triggered efforts to target TAMs and their associated molecules to modulate tumor progression. In particular, "re-education" to activate their anti-tumor potential or elimination of tumor promoting TAMs are strategies undergoing preclinical and clinical evaluation. Proof-of-principle studies indicate that TAM-centered therapeutic strategies may contribute to cancer therapy.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Immunity. 2013 Jan 24;38(1):79-91 - PubMed
    1. Cancer Res. 2009 Jun 1;69(11):4800-9 - PubMed
    1. Cancer Cell. 2008 Oct 7;14(4):299-311 - PubMed
    1. Eur J Immunol. 2011 Aug;41(8):2155-64 - PubMed
    1. Blood. 2008 Jun 15;111(12):5457-66 - PubMed

Publication types

LinkOut - more resources