Language

English

Publication Date

10-1-2025

Journal

Redox Biology

DOI

40930029

PMID

PMC12454664

PMCID

PMC12454664

PubMedCentral® Posted Date

9-8-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Tumor associated macrophages (TAMs) directly contribute to the dismal prognosis of glioblastoma by preventing anti-tumor immunity and promoting tumor invasion and angiogenesis. Inhibiting TAM infiltration is a potential therapeutic strategy in glioblastoma, with several chemokine antagonists in early clinical development. Hydrogen sulfide, a gasotransmitter that regulates microglial accumulation in a wide range of CNS diseases, may be a novel therapeutic target to prevent TAM recruitment in glioblastoma. In this study, hydrogen sulfide concentrations were directly measured from 14 isocitrate dehydrogenase (IDH)-wildtype glioblastoma surgical samples and compared against overall survival as well as expression of TAM markers and chemokines. Effects of hydrogen sulfide donor therapy on survival and TAM recruitment were also examined in a genetically engineered mouse model of glioblastoma. High hydrogen sulfide concentrations conferred a survival benefit in IDH-wildtype glioblastoma, in association with reduced monocyte-derived TAM density and downregulation of CXCL12. These findings were validated by administering hydrogen sulfide donor SG1002 to an immunocompetent mouse model of glioblastoma, which improved survival, inhibited monocyte infiltration, and downregulated CXCL12. Finally, hydrogen sulfide donor treatment directly reduced CXCL12 expression in glioblastoma cells, diminishing their ability to recruit monocytes in vitro. Taken together, these results demonstrate that hydrogen sulfide signaling prevents monocyte-derived TAM accumulation in glioblastoma by inhibiting chemotaxis.

Keywords

Hydrogen Sulfide, Glioblastoma, Animals, Mice, Humans, Chemokine CXCL12, Tumor-Associated Macrophages, Cell Line, Tumor, Monocytes, Brain Neoplasms, Disease Models, Animal, Down-Regulation, Gene Expression Regulation, Neoplastic, Female, Male, Hydrogen sulfide, Tumor associated macrophage, Glioblastoma

Published Open-Access

yes

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