GNAS knockout potentiates HDAC3 inhibition through viral mimicry-related interferon responses in lymphoma

Leukemia. 2024 Oct;38(10):2210-2224. doi: 10.1038/s41375-024-02325-4. Epub 2024 Aug 8.

Abstract

Despite selective HDAC3 inhibition showing promise in a subset of lymphomas with CREBBP mutations, wild-type tumors generally exhibit resistance. Here, using unbiased genome-wide CRISPR screening, we identify GNAS knockout (KO) as a sensitizer of resistant lymphoma cells to HDAC3 inhibition. Mechanistically, GNAS KO-induced sensitization is independent of the canonical G-protein activities but unexpectedly mediated by viral mimicry-related interferon (IFN) responses, characterized by TBK1 and IRF3 activation, double-stranded RNA formation, and transposable element (TE) expression. GNAS KO additionally synergizes with HDAC3 inhibition to enhance CD8+ T cell-induced cytotoxicity. Moreover, we observe in human lymphoma patients that low GNAS expression is associated with high baseline TE expression and upregulated IFN signaling and shares common disrupted biological activities with GNAS KO in histone modification, mRNA processing, and transcriptional regulation. Collectively, our findings establish an unprecedented link between HDAC3 inhibition and viral mimicry in lymphoma. We suggest low GNAS expression as a potential biomarker that reflects viral mimicry priming for enhanced response to HDAC3 inhibition in the clinical treatment of lymphoma, especially the CREBBP wild-type cases.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Chromogranins* / genetics
  • GTP-Binding Protein alpha Subunits, Gs* / genetics
  • GTP-Binding Protein alpha Subunits, Gs* / metabolism
  • Gene Knockout Techniques
  • Histone Deacetylase Inhibitors / pharmacology
  • Histone Deacetylases* / genetics
  • Histone Deacetylases* / metabolism
  • Humans
  • Interferons / metabolism
  • Lymphoma* / genetics
  • Lymphoma* / metabolism
  • Lymphoma* / pathology
  • Lymphoma* / virology
  • Mice
  • Signal Transduction

Substances

  • histone deacetylase 3
  • Histone Deacetylases
  • GTP-Binding Protein alpha Subunits, Gs
  • Chromogranins
  • GNAS protein, human
  • Interferons
  • Histone Deacetylase Inhibitors