Quinacrine-CASIN combination overcomes chemoresistance in human acute lymphoid leukemia

Limei Wu, Srinivas Chatla, Qiqi Lin, Fabliha Ahmed Chowdhury, Werner Geldenhuys and Wei Du ()
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Limei Wu: University of Pittsburgh School of Medicine
Srinivas Chatla: Lewis Katz School of Medicine at Temple University
Qiqi Lin: West Virginia University
Fabliha Ahmed Chowdhury: West Virginia University
Werner Geldenhuys: West Virginia University
Wei Du: University of Pittsburgh School of Medicine

Nature Communications, 2021, vol. 12, issue 1, 1-13

Abstract: Abstract Chemoresistance posts a major hurdle for treatment of acute leukemia. There is increasing evidence that prolonged and intensive chemotherapy often fails to eradicate leukemic stem cells, which are protected by the bone marrow niche and can induce relapse. Thus, new therapeutic approaches to overcome chemoresistance are urgently needed. By conducting an ex vivo small molecule screen, here we have identified Quinacrine (QC) as a sensitizer for Cytarabine (AraC) in treating acute lymphoblastic leukemia (ALL). We show that QC enhances AraC-mediated killing of ALL cells, and subsequently abrogates AraC resistance both in vitro and in an ALL-xenograft model. However, while combo AraC+QC treatment prolongs the survival of primary transplanted recipients, the combination exhibits limited efficacy in secondary transplanted recipients, consistent with the survival of niche-protected leukemia stem cells. Introduction of Cdc42 Activity Specific Inhibitor, CASIN, enhances the eradication of ALL leukemia stem cells by AraC+QC and prolongs the survival of both primary and secondary transplanted recipients without affecting normal long-term human hematopoiesis. Together, our findings identify a small-molecule regimen that sensitizes AraC-mediated leukemia eradication and provide a potential therapeutic approach for better ALL treatment.

Date: 2021
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DOI: 10.1038/s41467-021-27300-w

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