Chemotherapy resistance in acute myeloid leukemia is mediated by A20 suppression of spontaneous necroptosis

Nat Commun. 2024 Oct 24;15(1):9189. doi: 10.1038/s41467-024-53629-z.

Abstract

Acute myeloid leukemia (AML) is a deadly hematopoietic malignancy. Although many patients achieve complete remission with standard induction therapy, a combination of cytarabine and anthracycline, ~40% of patients have induction failure. These refractory patients pose a treatment challenge, as they do not respond to salvage therapy or allogeneic stem cell transplant. Herein, we show that AML patients who experience induction failure have elevated expression of the NF-κB target gene tumor necrosis factor alpha-induced protein-3 (TNFAIP3/A20) and impaired necroptotic cell death. A20High AML are resistant to anthracyclines, while A20Low AML are sensitive. Loss of A20 in AML restores sensitivity to anthracycline treatment by inducing necroptosis. Moreover, A20 prevents necroptosis in AML by targeting the necroptosis effector RIPK1, and anthracycline-induced necroptosis is abrogated in A20High AML. These findings suggest that NF-κB-driven A20 overexpression plays a role in failed chemotherapy induction and highlights the potential of targeting an alternative cell death pathway in AML.

MeSH terms

  • Animals
  • Anthracyclines / pharmacology
  • Cell Line, Tumor
  • Cytarabine / pharmacology
  • Cytarabine / therapeutic use
  • Drug Resistance, Neoplasm* / drug effects
  • Drug Resistance, Neoplasm* / genetics
  • Female
  • Humans
  • Leukemia, Myeloid, Acute* / drug therapy
  • Leukemia, Myeloid, Acute* / genetics
  • Leukemia, Myeloid, Acute* / metabolism
  • Leukemia, Myeloid, Acute* / pathology
  • Male
  • Mice
  • Middle Aged
  • NF-kappa B* / metabolism
  • Necroptosis* / drug effects
  • Receptor-Interacting Protein Serine-Threonine Kinases* / genetics
  • Receptor-Interacting Protein Serine-Threonine Kinases* / metabolism
  • Tumor Necrosis Factor alpha-Induced Protein 3* / genetics
  • Tumor Necrosis Factor alpha-Induced Protein 3* / metabolism

Substances

  • Tumor Necrosis Factor alpha-Induced Protein 3
  • TNFAIP3 protein, human
  • NF-kappa B
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Anthracyclines
  • Cytarabine
  • RIPK1 protein, human