FLT3 inhibitors upregulate CXCR4 and E-selectin ligands via ERK suppression in AML cells and CXCR4/E-selectin inhibition enhances anti-leukemia efficacy of FLT3-targeted therapy in AML

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Veröffentlicht in:Leukemia 2023-06, Vol.37 (6), p.1379-1383
Hauptverfasser: Jia, Yannan, Zhang, Weiguo, Basyal, Mahesh, Chang, Kyung Hee, Ostermann, Lauren, Burks, Jared K., Ly, Charlie, Mu-Mosley, Hong, Zhang, Qi, Han, Xin, Fogler, William E., Magnani, John L., Lesegretain, Arnaud, Zal, Anna A., Zal, Tomasz, Andreeff, Michael
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container_title Leukemia
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creator Jia, Yannan
Zhang, Weiguo
Basyal, Mahesh
Chang, Kyung Hee
Ostermann, Lauren
Burks, Jared K.
Ly, Charlie
Mu-Mosley, Hong
Zhang, Qi
Han, Xin
Fogler, William E.
Magnani, John L.
Lesegretain, Arnaud
Zal, Anna A.
Zal, Tomasz
Andreeff, Michael
description
doi_str_mv 10.1038/s41375-023-01897-x
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ispartof Leukemia, 2023-06, Vol.37 (6), p.1379-1383
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subjects 631/67/1059/2326
692/308/575
96
96/100
96/106
96/2
96/21
96/31
96/35
96/44
96/63
96/95
Acute myeloid leukemia
Cancer Research
Cancer therapies
Cell adhesion & migration
Chemokines
Critical Care Medicine
CXCR4 protein
Cytokines
Drug dosages
E-Selectin
fms-Like Tyrosine Kinase 3
Hematology
Humans
Hypotheses
Hypoxia
Intensive
Internal Medicine
Letter
Leukemia
Leukemia, Myeloid, Acute - drug therapy
Ligands
MAP Kinase Signaling System
Medical prognosis
Medicine
Medicine & Public Health
Mutation
Oncology
Patients
Protein Kinase Inhibitors - pharmacology
Receptors, CXCR4 - genetics
Signal Transduction
title FLT3 inhibitors upregulate CXCR4 and E-selectin ligands via ERK suppression in AML cells and CXCR4/E-selectin inhibition enhances anti-leukemia efficacy of FLT3-targeted therapy in AML
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