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Updated: Jul 3, 2025

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
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.
Abstract:
Acute leukemia continues to be a major cause of death from disease worldwide and current chemotherapeutic agents are associated with significant morbidity in survivors. While better and safer treatments for acute leukemia are urgently needed, standard drug development pipelines are lengthy and drug repurposing therefore provides a promising approach. Our previous evaluation of FDA-approved drugs for their antileukemic activity identified disulfiram, used for the treatment of alcoholism, as a candidate hit compound. This study assessed the biological effects of disulfiram on leukemia cells and evaluated its potential as a treatment strategy. We found that disulfiram inhibits the viability of a diverse panel of acute lymphoblastic and myeloid leukemia cell lines (n = 16) and patient-derived xenograft cells from patients with poor outcome and treatment-resistant disease (n = 15). The drug induced oxidative stress and apoptosis in leukemia cells within hours of treatment and was able to potentiate the effects of daunorubicin, etoposide, topotecan, cytarabine, and mitoxantrone chemotherapy. Upon combining disulfiram with auranofin, a drug approved for the treatment of rheumatoid arthritis that was previously shown to exert antileukemic effects, strong and consistent synergy was observed across a diverse panel of acute leukemia cell lines, the mechanism of which was based on enhanced ROS induction. Acute leukemia cells were more sensitive to the cytotoxic activity of disulfiram than solid cancer cell lines and non-malignant cells. While disulfiram is currently under investigation in clinical trials for solid cancers, this study provides evidence for the potential of disulfiram for acute leukemia treatment. KEY MESSAGES: Disulfiram induces rapid apoptosis in leukemia cells by boosting oxidative stress. Disulfiram inhibits leukemia cell growth more potently than solid cancer cell growth. Disulfiram can enhance the antileukemic efficacy of chemotherapies. Disulfiram strongly synergises with auranofin in killing acute leukemia cells by ROS induction. We propose testing of disulfiram in clinical trial for patients with acute leukemia.
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.
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