Unraveling the impact of crizotinib to promote megakaryopoiesis for alleviating thrombocytopenia in myelodysplastic neoplasms

Current therapeutic options for myelodysplastic neoplasms (MDS)-associated thrombocytopenia are limited. Megakaryocyte maturation might be an innovative therapeutic strategy because its dysregulation profoundly contributes to MDS pathogenesis. Here, we identified crizotinib, a clinically approved anti-cancer drug for anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer, as a potent inducer of megakaryocyte maturation. We demonstrated that crizotinib effectively induced polyploidization to increase the platelet-producing capacity of megakaryocytes derived from an MDS murine model and MDS patients by targeting Aurora kinases rather than its canonical targets, ALK/ROS1/c-MET. Importantly, crizotinib administration substantially ameliorated thrombocytopenia in our preclinical model. Our findings underscore the remarkable potential of crizotinib for drug repurposing and offer a novel therapeutic strategy for MDS patients with thrombocytopenia facing health-related quality of life concerns.

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Journal
Leukemia
Published
2025-08-14
DOI
https://doi.org/10.1038/s41375-025-02729-w
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
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article

Unraveling the impact of crizotinib to promote megakaryopoiesis for alleviating thrombocytopenia in myelodysplastic neoplasms

Hiroki Kobayashi, Minoru Yoshida, Yoshihiro Hayashi, Hironori Harada et al.
Leukemia
Acute Myeloid Leukemia Research
article

Unraveling the impact of crizotinib to promote megakaryopoiesis for alleviating thrombocytopenia in myelodysplastic neoplasms

Hiroki Kobayashi, Minoru Yoshida, Yoshihiro Hayashi, Hironori Harada, N Watanabe, Yuka Harada, Yasushige Kamimura-Aoyagi, Kanako Yuki, Yu Miyata, Yoshiya Ohnuma, Yuta Komizo
article en

Abstract

Current therapeutic options for myelodysplastic neoplasms (MDS)-associated thrombocytopenia are limited. Megakaryocyte maturation might be an innovative therapeutic strategy because its dysregulation profoundly contributes to MDS pathogenesis. Here, we identified crizotinib, a clinically approved anti-cancer drug for anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer, as a potent inducer of megakaryocyte maturation. We demonstrated that crizotinib effectively induced polyploidization to increase the platelet-producing capacity of megakaryocytes derived from an MDS murine model and MDS patients by targeting Aurora kinases rather than its canonical targets, ALK/ROS1/c-MET. Importantly, crizotinib administration substantially ameliorated thrombocytopenia in our preclinical model. Our findings underscore the remarkable potential of crizotinib for drug repurposing and offer a novel therapeutic strategy for MDS patients with thrombocytopenia facing health-related quality of life concerns.

LeukemiaVol. 39(11)
Ritsumeikan University (JP), Tokyo University of Pharmacy and Life Sciences (JP), Tokyo Metropolitan Komagome Hospital (JP), RIKEN Center for Sustainable Resource Science (JP)
Nippon Shinyaku, Tokyo Metropolitan Government, University of Tokyo, National Institutes of Health, Japan Society for the Promotion of Science
Openalex Percentile: Top 75%
Acute Myeloid Leukemia Research
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