FDA-approved disulfiram as a novel treatment for aggressive leukemia

Mawar Karsa1,2, Lin Xiao1,2, Emma Ronca1

  • 1Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Sydney, Sydney, NSW, Australia.

Journal of Molecular Medicine (Berlin, Germany)
|February 13, 2024
PubMed

Insights

Disulfiram, an alcoholism drug, shows promise for treating acute leukemia by rapidly inducing cell death and enhancing chemotherapy. It synergizes with auranofin, offering a potential new treatment strategy for this deadly disease.

Area of Science:

  • Hematology
  • Oncology
  • Pharmacology

Background:

  • Acute leukemia remains a significant global health challenge with current treatments causing substantial morbidity.
  • Drug repurposing offers a faster alternative to traditional drug development for novel leukemia therapies.
  • Disulfiram, an FDA-approved drug for alcoholism, was identified as a potential antileukemic agent.

Purpose of the Study:

  • To evaluate the biological effects of disulfiram on acute leukemia cells.
  • To assess disulfiram's potential as a standalone or combination therapy for acute leukemia.
  • To investigate the synergistic effects of disulfiram with other antileukemic agents, particularly auranofin.

Main Methods:

  • Testing disulfiram's effect on a panel of acute lymphoblastic and myeloid leukemia cell lines (n=16) and patient-derived xenograft cells (n=15).
  • Assessing disulfiram's induction of oxidative stress and apoptosis in leukemia cells.
  • Evaluating the potentiation of standard chemotherapies (daunorubicin, etoposide, topotecan, cytarabine, mitoxantrone) by disulfiram.
  • Investigating the synergistic effects of disulfiram combined with auranofin on leukemia cell lines.

Main Results:

  • Disulfiram significantly inhibited the viability of diverse acute leukemia cell lines and patient-derived xenografts.
  • Disulfiram rapidly induced oxidative stress and apoptosis in leukemia cells within hours.
  • Disulfiram potentiated the efficacy of several standard chemotherapeutic agents.
  • Strong synergy was observed between disulfiram and auranofin, mediated by enhanced reactive oxygen species (ROS) induction.
  • Leukemia cells exhibited greater sensitivity to disulfiram than solid cancer cells and non-malignant cells.

Conclusions:

  • Disulfiram demonstrates potent antileukemic activity through rapid induction of apoptosis via oxidative stress.
  • Disulfiram exhibits greater efficacy against leukemia cells compared to solid tumors and normal cells.
  • Disulfiram can enhance the effectiveness of existing chemotherapies and shows strong synergy with auranofin.
  • Disulfiram represents a promising candidate for clinical trials in patients with acute leukemia.