Reprogramming cellular senescence in the tumor microenvironment augments cancer immunotherapy through multifunctional nanocrystals.
Tumor Microenvironment
/ drug effects
Nanoparticles
/ chemistry
Immunotherapy
/ methods
Cellular Senescence
/ drug effects
Animals
Humans
Mice
Cell Line, Tumor
Neoplasms
/ immunology
Pyrimidines
/ pharmacology
Cellular Reprogramming
/ drug effects
Janus Kinase 2
/ metabolism
Nitriles
/ pharmacology
Pyrazoles
/ pharmacology
CD8-Positive T-Lymphocytes
/ immunology
STAT3 Transcription Factor
/ metabolism
Azepines
Journal
Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440
Informations de publication
Date de publication:
Nov 2024
Nov 2024
Historique:
medline:
2
11
2024
pubmed:
2
11
2024
entrez:
1
11
2024
Statut:
ppublish
Résumé
Harnessing the immunogenic potential of senescent tumor cells provides an opportunity to remodel tumor microenvironment (TME) and boost antitumor immunity. However, this potential needs to be sophisticatedly wielded to avoid additional immunosuppressive capacity of senescent cells. Our study shows that blocking the JAK2/STAT3 pathway enhances immunogenic efficacy of Aurora kinase inhibitor alisertib (Ali)-induced senescence by reducing immunosuppressive senescence-associated secretory phenotype (SASP) while preserving immunogenic SASP. Hypothesizing that SASP reprogramming with Ali and JAK2 inhibitor ruxolitinib (Rux) will benefit cancer immunotherapy, we create nanoparticulate crystals (Ali-Rux) composed of Ali and Rux with a fully active pharmaceutical ingredient. Immunization with Ali-Rux-orchestrated senescent cells promotes stronger activation of antigen-presenting cells, enhancing antitumor immune surveillance. This approach remodels the TME by increasing CD8
Identifiants
pubmed: 39485841
doi: 10.1126/sciadv.adp7022
doi:
Substances chimiques
Pyrimidines
0
MLN 8237
0
Janus Kinase 2
EC 2.7.10.2
ruxolitinib
82S8X8XX8H
Nitriles
0
Pyrazoles
0
STAT3 Transcription Factor
0
Azepines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM