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PMID: 18467122 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Macrophage polarization in tumour progression.

Seminars in cancer biology ·Vol. 18 ·No. 5 ·2008-10-00 ·Pages 349-55

Sica A, Larghi P, Mancino A, Rubino L, Porta C, Totaro MG, Rimoldi M, Biswas SK, Allavena P, Mantovani A

Abstract

Macrophages are a fundamental part of the innate defense mechanisms, which can promote specific immunity by inducing T cell recruitment and activation. Despite this, their presence within the tumour microenvironment has been associated with enhanced tumour progression and shown to promote cancer cell growth and spread, angiogenesis and immunosuppression. This paradoxical role of macrophages in cancer finds an explanation in their functional plasticity, that may result in the polarized expression of either pro- or anti-tumoural functions. Key players in the setting of their phenotype are the microenvironmental signals to which macrophages are exposed, which selectively tune their functions within a functional spectrum encompassing the M1 and M2 extremes. Here, we discuss recent findings suggesting that targeting tumour-associated macrophages (TAMs) polarization may represent a novel therapeutic strategy against cancer.

MeSH Terms
Animals Cytokines/immunology,metabolism Disease Progression Humans Immunity, Active Inflammation/immunology,metabolism Intercellular Signaling Peptides and Proteins/metabolism Macrophage Activation Macrophages/immunology,physiology Monocytes/immunology,metabolism Neoplasms/immunology,physiopathology
Chemicals
Cytokines Intercellular Signaling Peptides and Proteins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Sica Antonio
Department of Inflammation and Immunology, Fondazione Humanitas per la Ricerca, 20089 Rozzano, Milan, Italy. antonio.sica@humanitas.it
Larghi Paola
Mancino Alessandra
Rubino Luca
Porta Chiara
Totaro Maria Grazia
Rimoldi Monica
Biswas Subhra Kumar
Allavena Paola
Mantovani Alberto
Article Info
Journal
Seminars in cancer biology
Abbr.
Semin Cancer Biol
ISSN
1096-3650
Published
2008-10-00
Epub
2008-00-26
Pages
349-55
Language
English
Region
England
NLM ID
9010218
Subset
IM
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