Lipid-loaded macrophages as new therapeutic target in cancer.

Immunomodulation Macrophages Metabolic Networks and Pathways Tumor Microenvironment

Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
07 2022
Historique:
accepted: 31 05 2022
entrez: 7 7 2022
pubmed: 8 7 2022
medline: 12 7 2022
Statut: ppublish

Résumé

Macrophages are main players of the innate immune system. They show great heterogeneity and play diverse functions that include support to development, sustenance of tissue homeostasis and defense against infections. Dysfunctional macrophages have been described in multiple pathologies including cancer. Indeed tumor-associated macrophages (TAMs) are abundant in most tumors and sustain cancer growth, promote invasion and mediate immune evasion. Importantly, lipid metabolism influences macrophage activation and lipid accumulation confers pathogenic features on macrophages. Notably, a subset of lipid-loaded macrophages has been recently identified in many tumor types. Lipid-loaded TAMs support tumor growth and progression and exert immune-suppressive activities. In this review, we describe the role of lipid metabolism in macrophage activation in physiology and pathology and we discuss the impact of lipid accumulation in macrophages in the context of cancer.

Identifiants

pubmed: 35798535
pii: jitc-2022-004584
doi: 10.1136/jitc-2022-004584
pmc: PMC9263925
pii:
doi:

Substances chimiques

Lipids 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Giulia Marelli (G)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy.

Nicolò Morina (N)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy.
Department of Biomedical Sciences, Humanitas University, Lombardia, Italy.

Federica Portale (F)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy.

Marta Pandini (M)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy.
Department of Biomedical Sciences, Humanitas University, Lombardia, Italy.

Marta Iovino (M)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy.

Giusy Di Conza (G)

Department of Oncology, University of Lausanne, Lausanne, Switzerland.
Ludwig Institute of Cancer Research, University of Lausanne, Lausanne, Switzerland.

Ping-Chih Ho (PC)

Department of Oncology, University of Lausanne, Lausanne, Switzerland.
Ludwig Institute of Cancer Research, University of Lausanne, Lausanne, Switzerland.

Diletta Di Mitri (D)

Tumor Microenvironment Unit, IRCCS Humanitas Research Hospital, Lombardia, Italy diletta.di_mitri@humanitasresearch.it.
Department of Biomedical Sciences, Humanitas University, Lombardia, Italy.

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