Skip to main navigation Skip to search Skip to main content

The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages

Research output: Contribution to journalReview articlepeer-review

Abstract

The link between inflammation and cancer proposed more than a century ago by Rudolf Virchow, who noticed the infiltration of leukocytes in malignant tissues, has recently found a number of genetic and molecular confirmations. Experimental, clinical and epidemiological studies have revealed that chronic inflammation contributes to cancer progression and even predisposes to different types of cancer. Cancer-associated inflammation includes: the presence of leukocyte infiltration; the expression of cytokines such as tumor necrosis factor (TNF) or interleukin (IL)-1; chemokines such as CCL2 and CXCL8; active tissue remodelling and neo-angiogenesis. Tumor-associated macrophages (TAM) are key regulators of the link between inflammation and cancer. Many observations indicate that, in the tumor micro-environment, TAM have several protumoral functions, including expression of growth factors, matrix proteases, promotion of angiogenesis and suppression of adaptive immunity. In this review we will discuss the role of TAM in the inflammatory micro-environment of solid tumors and will try to identify potential target for future therapeutic approaches.

Original languageEnglish
Pages (from-to)1-9
Number of pages9
JournalCritical Reviews in Oncology/Hematology
Volume66
Issue number1
DOIs
Publication statusPublished - Apr 2008
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Angiogenesis
  • Chemokines
  • Cytokines
  • Inflammation
  • Matrix-metallo proteases (MMP)
  • Micro-environment
  • Tumor-associated macrophages (TAM)
  • tumor

Fingerprint

Dive into the research topics of 'The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages'. Together they form a unique fingerprint.

Cite this