ArticleJournal of experimental & clinical cancer research : CR2026
Exosomal NEAT1 from tumor stem cells induces SIRPA
Article in Journal of experimental & clinical cancer research : CR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundSignal Regulatory Protein Alpha (SIRPA) functions as an inhibitory receptor to suppress phagocytosis of macrophages and promote tumor immune evasion. Recent studies revealed that SIRPA deficiency reprogrammed tumor-associated macrophages toward an antitumor phenotype, and SIRPA functioned independently of CD47. However, the exact role and signaling pathways by which SIRPA
methodsPublic single-cell RNA sequencing datasets were analyzed to identify SIRPA
resultsBioinformatic analysis of single-cell datasets identified a distinct subset of SIRPA
conclusionsGSC-derived exosomal NEAT1 reprogrammed macrophages toward an immunosuppressive SIRPA
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