Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V

Receptor tyrosine kinase mutations are frequent and associated with poor prognosis in acute myeloid leukemia (AML). Here the authors show that the antipsychotic drug chlorpromazine reduces AML cells viability by perturbing the intracellular localization of FLT3-ITD and KIT-D816V.

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Autores principales: Shinya Rai, Hirokazu Tanaka, Mai Suzuki, J. Luis Espinoza, Takahiro Kumode, Akira Tanimura, Takafumi Yokota, Kenji Oritani, Toshio Watanabe, Yuzuru Kanakura, Itaru Matsumura
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/8d959de3d6524e5897ad361f125459c1
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spelling oai:doaj.org-article:8d959de3d6524e5897ad361f125459c12021-12-02T15:10:55ZChlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V10.1038/s41467-020-17666-82041-1723https://doaj.org/article/8d959de3d6524e5897ad361f125459c12020-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-17666-8https://doaj.org/toc/2041-1723Receptor tyrosine kinase mutations are frequent and associated with poor prognosis in acute myeloid leukemia (AML). Here the authors show that the antipsychotic drug chlorpromazine reduces AML cells viability by perturbing the intracellular localization of FLT3-ITD and KIT-D816V.Shinya RaiHirokazu TanakaMai SuzukiJ. Luis EspinozaTakahiro KumodeAkira TanimuraTakafumi YokotaKenji OritaniToshio WatanabeYuzuru KanakuraItaru MatsumuraNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Shinya Rai
Hirokazu Tanaka
Mai Suzuki
J. Luis Espinoza
Takahiro Kumode
Akira Tanimura
Takafumi Yokota
Kenji Oritani
Toshio Watanabe
Yuzuru Kanakura
Itaru Matsumura
Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
description Receptor tyrosine kinase mutations are frequent and associated with poor prognosis in acute myeloid leukemia (AML). Here the authors show that the antipsychotic drug chlorpromazine reduces AML cells viability by perturbing the intracellular localization of FLT3-ITD and KIT-D816V.
format article
author Shinya Rai
Hirokazu Tanaka
Mai Suzuki
J. Luis Espinoza
Takahiro Kumode
Akira Tanimura
Takafumi Yokota
Kenji Oritani
Toshio Watanabe
Yuzuru Kanakura
Itaru Matsumura
author_facet Shinya Rai
Hirokazu Tanaka
Mai Suzuki
J. Luis Espinoza
Takahiro Kumode
Akira Tanimura
Takafumi Yokota
Kenji Oritani
Toshio Watanabe
Yuzuru Kanakura
Itaru Matsumura
author_sort Shinya Rai
title Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
title_short Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
title_full Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
title_fullStr Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
title_full_unstemmed Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
title_sort chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of flt3-itd and kit-d816v
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/8d959de3d6524e5897ad361f125459c1
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