Immunoediting instructs tumor metabolic reprogramming to support immune evasion.
Détails
ID Serval
serval:BIB_E4E3E6C91256
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Immunoediting instructs tumor metabolic reprogramming to support immune evasion.
Périodique
Cell metabolism
ISSN
1932-7420 (Electronic)
ISSN-L
1550-4131
Statut éditorial
Publié
Date de publication
03/01/2023
Peer-reviewed
Oui
Volume
35
Numéro
1
Pages
118-133.e7
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
Immunoediting sculpts immunogenicity and thwarts host anti-tumor responses in tumor cells during tumorigenesis; however, it remains unknown whether metabolic programming of tumor cells can be guided by immunosurveillance. Here, we report that T cell-mediated immunosurveillance in early-stage tumorigenesis instructs c-Myc upregulation and metabolic reprogramming in tumor cells. This previously unexplored tumor-immune interaction is controlled by non-canonical interferon gamma (IFNγ)-STAT3 signaling and supports tumor immune evasion. Our findings uncover that immunoediting instructs deregulated bioenergetic programs in tumor cells to empower them to disarm the T cell-mediated immunosurveillance by imposing metabolic tug-of-war between tumor and infiltrating T cells and forming the suppressive tumor microenvironment.
Mots-clé
Humans, Immune Evasion, Neoplasms/pathology, Interferon-gamma/metabolism, T-Lymphocytes/metabolism, Carcinogenesis, Cell Transformation, Neoplastic, Tumor Microenvironment, IFNγ, Myc, STAT3, immunoediting, immunosurveillance, tumor immunology
Pubmed
Web of science
Création de la notice
17/01/2023 15:39
Dernière modification de la notice
28/02/2023 6:51