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Wyszukujesz frazę ""fms-Like Tyrosine Kinase 3"" wg kryterium: Temat


Tytuł:
Gene expression profiling identifies FLT3 mutation-like cases in wild-type FLT3 acute myeloid leukemia.
Autorzy:
Mosquera Orgueira A; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
Peleteiro Raíndo A; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
Cid López M; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
Antelo Rodríguez B; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
Díaz Arias JÁ; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Ferreiro Ferro R; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Alonso Vence N; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Bendaña López Á; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Abuín Blanco A; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Bao Pérez L; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Melero Valentín P; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.
González Pérez MS; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.
Cerchione C; University of Bologna, Bologna, Italy.
Martinelli G; Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Meldola, Italy.
Montesinos Fernández P; University Hospital of La Fe in Valencia, Valencia, Spain.
Pérez Encinas MM; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
Bello López JL; Health Research Institute of Santiago de Compostela (IDIS), Santiago, Spain.; Division of Hematology, Complexo Hospitalario Universitario de Santiago de Compostela (CHUS), SERGAS, Santiago, Spain.; University of Santiago de Compostela, Santiago, Spain.
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Źródło:
PloS one [PLoS One] 2021 Feb 16; Vol. 16 (2), pp. e0247093. Date of Electronic Publication: 2021 Feb 16 (Print Publication: 2021).
Typ publikacji:
Journal Article
MeSH Terms:
Leukemia/*genetics
Leukemia, Myeloid, Acute/*genetics
Mutation/*genetics
fms-Like Tyrosine Kinase 3/*genetics
Biomarkers/metabolism ; DNA (Cytosine-5-)-Methyltransferases/genetics ; DNA Methyltransferase 3A ; Gene Expression Profiling/methods ; Humans ; Nuclear Proteins/genetics ; Nucleophosmin ; Staurosporine/analogs & derivatives ; Staurosporine/pharmacology ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors
Czasopismo naukowe
Tytuł:
Expression of myeloid Src-family kinases is associated with poor prognosis in AML and influences Flt3-ITD kinase inhibitor acquired resistance.
Autorzy:
Patel RK; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Weir MC; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Shen K; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Snyder D; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Cooper VS; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Smithgall TE; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
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Źródło:
PloS one [PLoS One] 2019 Dec 02; Vol. 14 (12), pp. e0225887. Date of Electronic Publication: 2019 Dec 02 (Print Publication: 2019).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Leukemia, Myeloid, Acute*/diagnosis
Leukemia, Myeloid, Acute*/drug therapy
Leukemia, Myeloid, Acute*/enzymology
Leukemia, Myeloid, Acute*/genetics
Mutation, Missense*
Proto-Oncogene Proteins*/biosynthesis
Proto-Oncogene Proteins*/genetics
Proto-Oncogene Proteins c-hck*/biosynthesis
Proto-Oncogene Proteins c-hck*/genetics
fms-Like Tyrosine Kinase 3*/antagonists & inhibitors
fms-Like Tyrosine Kinase 3*/genetics
fms-Like Tyrosine Kinase 3*/metabolism
src-Family Kinases*/biosynthesis
src-Family Kinases*/genetics
Drug Resistance, Neoplasm/*drug effects
Gene Expression Regulation, Developmental/*drug effects
Gene Expression Regulation, Leukemic/*drug effects
Protein Kinase Inhibitors/*pharmacology
Pyrimidines/*pharmacology
Pyrroles/*pharmacology
Amino Acid Substitution ; Cell Line, Tumor ; Drug Resistance, Neoplasm/genetics ; Humans ; Prognosis ; Exome Sequencing
Czasopismo naukowe
Tytuł:
Fast in-vitro screening of FLT3-ITD inhibitors using silkworm-baculovirus protein expression system.
Autorzy:
Yamamoto N; Division of Biophysics, Department of Physiology, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Kikuchi J; Division of Stem Cell Regulation, Center for Molecular Medicine, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Furukawa Y; Division of Stem Cell Regulation, Center for Molecular Medicine, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Shibayama N; Division of Biophysics, Department of Physiology, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
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Źródło:
PloS one [PLoS One] 2022 May 05; Vol. 17 (5), pp. e0261699. Date of Electronic Publication: 2022 May 05 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Bombyx*/genetics
Leukemia, Myeloid, Acute*/genetics
Animals ; Baculoviridae ; Mutation ; Protein Kinase Inhibitors/pharmacology ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
Regulation of the Flt3 Gene in Haematopoietic Stem and Early Progenitor Cells.
Autorzy:
Volpe G; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Clarke M; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Garcìa P; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Walton DS; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Vegiopoulos A; DKFZ Junior Group Metabolism and Stem Cell Plasticity, Division of Molecular Metabolic Control (A170), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Del Pozzo W; School of Physics and Astronomy, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
O'Neill LP; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Frampton J; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Dumon S; Institute of Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
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Źródło:
PloS one [PLoS One] 2015 Sep 18; Vol. 10 (9), pp. e0138257. Date of Electronic Publication: 2015 Sep 18 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
CCAAT-Enhancer-Binding Proteins/*physiology
Hematopoietic Stem Cells/*metabolism
Oncogene Proteins v-myb/*physiology
fms-Like Tyrosine Kinase 3/*genetics
Animals ; CCAAT-Enhancer-Binding Proteins/genetics ; Cell Differentiation/genetics ; Cell Lineage/genetics ; Cells, Cultured ; Gene Expression Regulation ; Hematopoiesis/genetics ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Oncogene Proteins v-myb/genetics ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Crystal structure of the FLT3 kinase domain bound to the inhibitor Quizartinib (AC220).
Autorzy:
Zorn JA; Department of Molecular and Cell Biology, University of California, Berkeley, California, United States of America; California Institute for Quantitative Biosciences, University of California, Berkeley, California, United States of America.
Wang Q; Department of Molecular and Cell Biology, University of California, Berkeley, California, United States of America; California Institute for Quantitative Biosciences, University of California, Berkeley, California, United States of America.
Fujimura E; Department of Molecular and Cell Biology, University of California, Berkeley, California, United States of America.
Barros T; Department of Molecular and Cell Biology, University of California, Berkeley, California, United States of America; California Institute for Quantitative Biosciences, University of California, Berkeley, California, United States of America; Howard Hughes Medical Institute, University of California, Berkeley, California, United States of America.
Kuriyan J; Department of Molecular and Cell Biology, University of California, Berkeley, California, United States of America; California Institute for Quantitative Biosciences, University of California, Berkeley, California, United States of America; Howard Hughes Medical Institute, University of California, Berkeley, California, United States of America; Department of Chemistry, University of California, Berkeley, California, United States of America; Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
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Źródło:
PloS one [PLoS One] 2015 Apr 02; Vol. 10 (4), pp. e0121177. Date of Electronic Publication: 2015 Apr 02 (Print Publication: 2015).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Antineoplastic Agents/*chemistry
Benzothiazoles/*chemistry
Neoplasm Proteins/*chemistry
Phenylurea Compounds/*chemistry
Protein Kinase Inhibitors/*chemistry
Recombinant Fusion Proteins/*chemistry
fms-Like Tyrosine Kinase 3/*chemistry
Animals ; Baculoviridae/genetics ; Catalytic Domain ; Crystallography, X-Ray ; Humans ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Mutation ; Neoplasm Proteins/antagonists & inhibitors ; Neoplasm Proteins/genetics ; Protein Binding ; Protein Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Recombinant Fusion Proteins/genetics ; Sf9 Cells ; Spodoptera/genetics ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
Targeting oncoprotein stability overcomes drug resistance caused by FLT3 kinase domain mutations.
Autorzy:
Yu C; Department Medicine I, University Medical Center Freiburg, Freiburg, Germany.
Kancha RK; Department Medicine I, University Medical Center Freiburg, Freiburg, Germany.
Duyster J; Department Medicine I, University Medical Center Freiburg, Freiburg, Germany.
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Źródło:
PloS one [PLoS One] 2014 May 21; Vol. 9 (5), pp. e97116. Date of Electronic Publication: 2014 May 21 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation, Leukemic*
Benzoquinones/*pharmacology
HSP90 Heat-Shock Proteins/*antagonists & inhibitors
Lactams, Macrocyclic/*pharmacology
fms-Like Tyrosine Kinase 3/*genetics
Amino Acid Sequence ; Animals ; Cell Line, Tumor ; Drug Resistance, Neoplasm/drug effects ; Drug Resistance, Neoplasm/genetics ; HSP90 Heat-Shock Proteins/genetics ; HSP90 Heat-Shock Proteins/metabolism ; Humans ; Leukemia, Myeloid, Acute/genetics ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/pathology ; Mice ; Molecular Sequence Data ; Mutation ; Protein Binding ; Protein Kinase Inhibitors/pharmacology ; Protein Stability/drug effects ; Protein Structure, Tertiary ; Proteolysis ; Sequence Alignment ; Signal Transduction ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancer.
Autorzy:
Lin WH; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Yeh TK; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Jiaang WT; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Yen KJ; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chen CH; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Huang CT; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Yen SC; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Hsieh SY; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chou LH; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chen CP; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chiu CH; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Kao LC; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chao YS; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Chen CT; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan.
Hsu JT; Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Taiwan ; Department of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.
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Źródło:
PloS one [PLoS One] 2014 Jan 08; Vol. 9 (1), pp. e83160. Date of Electronic Publication: 2014 Jan 08 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Antineoplastic Agents/*therapeutic use
Benzamides/*therapeutic use
Histone Deacetylase Inhibitors/*therapeutic use
Hydroxamic Acids/*therapeutic use
Leukemia, Myeloid, Acute/*drug therapy
Protein Kinase Inhibitors/*therapeutic use
Urea/*analogs & derivatives
fms-Like Tyrosine Kinase 3/*antagonists & inhibitors
Animals ; Antineoplastic Agents/pharmacokinetics ; Antineoplastic Agents/pharmacology ; Antineoplastic Combined Chemotherapy Protocols/pharmacology ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Apoptosis/drug effects ; Benzamides/chemistry ; Benzamides/pharmacokinetics ; Benzamides/pharmacology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Histone Deacetylase Inhibitors/pharmacology ; Hydroxamic Acids/pharmacology ; Leukemia, Myeloid, Acute/enzymology ; Leukemia, Myeloid, Acute/pathology ; Male ; Mice ; Mice, Nude ; Protein Kinase Inhibitors/pharmacology ; Rats ; Signal Transduction/drug effects ; Urea/chemistry ; Urea/pharmacokinetics ; Urea/pharmacology ; Urea/therapeutic use ; Vorinostat ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Inhibition of the PI3K/Akt/GSK3 pathway downstream of BCR/ABL, Jak2-V617F, or FLT3-ITD downregulates DNA damage-induced Chk1 activation as well as G2/M arrest and prominently enhances induction of apoptosis.
Autorzy:
Kurosu T; Department of Hematology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Nagao T
Wu N
Oshikawa G
Miura O
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Źródło:
PloS one [PLoS One] 2013 Nov 18; Vol. 8 (11), pp. e79478. Date of Electronic Publication: 2013 Nov 18 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Fusion Proteins, bcr-abl/*metabolism
Glycogen Synthase Kinase 3/*metabolism
Janus Kinase 2/*metabolism
Phosphatidylinositol 3-Kinases/*metabolism
Proto-Oncogene Proteins c-akt/*metabolism
fms-Like Tyrosine Kinase 3/*metabolism
Animals ; Apoptosis/drug effects ; Benzamides/pharmacology ; Cell Cycle/drug effects ; Cell Line ; Etoposide/pharmacology ; Flow Cytometry ; Fusion Proteins, bcr-abl/genetics ; Glycogen Synthase Kinase 3/genetics ; Imatinib Mesylate ; Immunoblotting ; Immunoprecipitation ; Janus Kinase 2/genetics ; Mice ; Nocodazole/pharmacology ; Phosphatidylinositol 3-Kinases/genetics ; Piperazines/pharmacology ; Proto-Oncogene Proteins c-akt/genetics ; Pyrimidines/pharmacology ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
Bcl11a controls Flt3 expression in early hematopoietic progenitors and is required for pDC development in vivo.
Autorzy:
Wu X; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Satpathy AT
Kc W
Liu P
Murphy TL
Murphy KM
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Źródło:
PloS one [PLoS One] 2013 May 31; Vol. 8 (5), pp. e64800. Date of Electronic Publication: 2013 May 31 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Gene Expression Regulation*/drug effects
Carrier Proteins/*genetics
Dendritic Cells/*metabolism
Hematopoietic Stem Cells/*metabolism
Nuclear Proteins/*genetics
fms-Like Tyrosine Kinase 3/*genetics
Animals ; Carrier Proteins/metabolism ; Cell Differentiation ; Cell Lineage/drug effects ; Cell Lineage/genetics ; DNA-Binding Proteins ; Dendritic Cells/cytology ; Dendritic Cells/drug effects ; Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology ; Hematopoietic Stem Cells/cytology ; Hematopoietic Stem Cells/drug effects ; Immunophenotyping ; Lymphoid Progenitor Cells/cytology ; Lymphoid Progenitor Cells/drug effects ; Lymphoid Progenitor Cells/metabolism ; Membrane Proteins/metabolism ; Membrane Proteins/pharmacology ; Mice ; Mice, Knockout ; Nuclear Proteins/metabolism ; Receptors, Interleukin-7/genetics ; Receptors, Interleukin-7/metabolism ; Repressor Proteins ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Association of the protein-tyrosine phosphatase DEP-1 with its substrate FLT3 visualized by in situ proximity ligation assay.
Autorzy:
Böhmer SA; Institute of Molecular Cell Biology, Center for Molecular Biomedicine, Jena University Hospital, Jena, Germany.
Weibrecht I
Söderberg O
Böhmer FD
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Źródło:
PloS one [PLoS One] 2013 May 01; Vol. 8 (5), pp. e62871. Date of Electronic Publication: 2013 May 01 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
fms-Like Tyrosine Kinase 3/*metabolism
Animals ; Apoptosis ; COS Cells ; Cell Proliferation ; Chlorocebus aethiops ; Fluorescent Antibody Technique, Indirect ; Humans ; Kinetics ; Membrane Proteins/physiology ; Microscopy, Fluorescence ; Oxidation-Reduction ; Protein Interaction Mapping ; Receptor-Like Protein Tyrosine Phosphatases, Class 3/metabolism ; Signal Transduction ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors
Czasopismo naukowe
Tytuł:
Reversible resistance induced by FLT3 inhibition: a novel resistance mechanism in mutant FLT3-expressing cells.
Autorzy:
Weisberg E; Department of Medical Oncology/Hematologic Neoplasia, Dana Farber Cancer Institute, Boston, Massachusetts, United States of America. ellen_ />Ray A
Nelson E
Adamia S
Barrett R
Sattler M
Zhang C
Daley JF
Frank D
Fox E
Griffin JD
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Źródło:
PloS one [PLoS One] 2011; Vol. 6 (9), pp. e25351. Date of Electronic Publication: 2011 Sep 28.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Mutation*
Drug Resistance, Neoplasm/*drug effects
Drug Resistance, Neoplasm/*genetics
Gene Expression Regulation, Neoplastic/*drug effects
Protein Kinase Inhibitors/*pharmacology
fms-Like Tyrosine Kinase 3/*antagonists & inhibitors
fms-Like Tyrosine Kinase 3/*genetics
Cell Line, Tumor ; Cell Proliferation/drug effects ; Enzyme Stability/drug effects ; Enzyme Stability/genetics ; Gene Expression Regulation, Neoplastic/genetics ; Half-Life ; Humans ; Leukemia, Myeloid, Acute/genetics ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/pathology ; Phosphorylation/drug effects ; Phosphorylation/genetics ; Piperazines/pharmacology ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Signal Transduction/drug effects ; Signal Transduction/genetics ; Staurosporine/analogs & derivatives ; Staurosporine/pharmacology ; Thiazoles/pharmacology ; Tyrosine/metabolism ; Up-Regulation/drug effects ; fms-Like Tyrosine Kinase 3/chemistry ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Selective Akt inhibitors synergize with tyrosine kinase inhibitors and effectively override stroma-associated cytoprotection of mutant FLT3-positive AML cells.
Autorzy:
Weisberg E; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA. ellen_ />Liu Q
Zhang X
Nelson E
Sattler M
Liu F
Nicolais M
Zhang J
Mitsiades C
Smith RW
Stone R
Galinsky I
Nonami A
Griffin JD
Gray N
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Źródło:
PloS one [PLoS One] 2013; Vol. 8 (2), pp. e56473. Date of Electronic Publication: 2013 Feb 21.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Protein Kinase Inhibitors/*administration & dosage
Proto-Oncogene Proteins c-akt/*metabolism
Stromal Cells/*cytology
Stromal Cells/*metabolism
fms-Like Tyrosine Kinase 3/*metabolism
Apoptosis/drug effects ; Benzothiazoles/administration & dosage ; Bone Marrow Cells/cytology ; Bone Marrow Cells/drug effects ; Bone Marrow Cells/metabolism ; Cell Communication/drug effects ; Cell Cycle/drug effects ; Cell Proliferation/drug effects ; Drug Screening Assays, Antitumor ; Drug Synergism ; Humans ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/pathology ; Phenylurea Compounds/administration & dosage ; Proto-Oncogene Proteins c-akt/antagonists & inhibitors ; Staurosporine/administration & dosage ; Staurosporine/analogs & derivatives ; Stromal Cells/drug effects ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
H2O2 production downstream of FLT3 is mediated by p22phox in the endoplasmic reticulum and is required for STAT5 signalling.
Autorzy:
Woolley JF; Tumour Biology Laboratory, Biochemistry Department, Bioscience Research Institute, University College, Cork, Ireland.
Naughton R
Stanicka J
Gough DR
Bhatt L
Dickinson BC
Chang CJ
Cotter TG
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Źródło:
PloS one [PLoS One] 2012; Vol. 7 (7), pp. e34050. Date of Electronic Publication: 2012 Jul 13.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation, Neoplastic/*drug effects
Hydrogen Peroxide/*metabolism
Leukemia, Myeloid, Acute/*genetics
NADPH Oxidases/*metabolism
STAT5 Transcription Factor/*metabolism
fms-Like Tyrosine Kinase 3/*metabolism
Benzoxazoles/pharmacology ; Cell Line, Tumor ; Endoplasmic Reticulum/drug effects ; Endoplasmic Reticulum/metabolism ; Fluorescent Dyes ; Gene Knockdown Techniques ; Glycogen Synthase Kinase 3/antagonists & inhibitors ; Glycogen Synthase Kinase 3/genetics ; Glycogen Synthase Kinase 3/metabolism ; Glycogen Synthase Kinase 3 beta ; Humans ; Imidazoles/pharmacology ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/pathology ; Mitochondria/drug effects ; Mitochondria/metabolism ; Mutation ; NADPH Oxidases/antagonists & inhibitors ; NADPH Oxidases/genetics ; Proteasome Endopeptidase Complex/drug effects ; Proteasome Endopeptidase Complex/metabolism ; Protein Kinase Inhibitors/pharmacology ; Protein Structure, Tertiary ; Proto-Oncogene Proteins c-pim-1/antagonists & inhibitors ; Proto-Oncogene Proteins c-pim-1/genetics ; Proto-Oncogene Proteins c-pim-1/metabolism ; Pyrroles/pharmacology ; RNA, Small Interfering/genetics ; STAT5 Transcription Factor/antagonists & inhibitors ; STAT5 Transcription Factor/genetics ; Signal Transduction/drug effects ; Staurosporine/analogs & derivatives ; Staurosporine/pharmacology ; Triazoles/pharmacology ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
Functional pathway analysis using SCNP of FLT3 receptor pathway deregulation in AML provides prognostic information independent from mutational status.
Autorzy:
Cesano A; Nodality, Inc, South San Francisco, California, United States of America.
Putta S
Rosen DB
Cohen AC
Gayko U
Mathi K
Woronicz J
Hawtin RE
Cripe L
Sun Z
Tallman MS
Paietta E
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Źródło:
PloS one [PLoS One] 2013; Vol. 8 (2), pp. e56714. Date of Electronic Publication: 2013 Feb 19.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation*
Signal Transduction*
Leukemia, Myeloid, Acute/*genetics
fms-Like Tyrosine Kinase 3/*genetics
Aged ; Aged, 80 and over ; Apoptosis ; Cells, Cultured ; Disease-Free Survival ; Female ; Humans ; Induction Chemotherapy ; Kaplan-Meier Estimate ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/mortality ; Male ; Middle Aged ; Multivariate Analysis ; Mutagenesis ; Nucleophosmin ; Principal Component Analysis ; Prognosis ; Single-Cell Analysis ; fms-Like Tyrosine Kinase 3/metabolism
Czasopismo naukowe
Tytuł:
Role of misfolded N-CoR mediated transcriptional deregulation of Flt3 in acute monocytic leukemia (AML)-M5 subtype.
Autorzy:
Nin DS; Cancer Science Institute, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Kok WK
Li F
Takahashi S
Chng WJ
Khan M
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Źródło:
PloS one [PLoS One] 2012; Vol. 7 (4), pp. e34501. Date of Electronic Publication: 2012 Apr 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Leukemia, Monocytic, Acute/*metabolism
Nuclear Receptor Co-Repressor 1/*metabolism
fms-Like Tyrosine Kinase 3/*metabolism
Cell Differentiation/genetics ; Cell Differentiation/physiology ; Cell Line ; Cell Line, Tumor ; Cell Proliferation ; Chromatin Immunoprecipitation ; Humans ; Leukemia, Monocytic, Acute/genetics ; Nuclear Receptor Co-Repressor 1/genetics ; Protein Binding ; RNA Interference ; Real-Time Polymerase Chain Reaction ; Reverse Transcriptase Polymerase Chain Reaction ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe
Tytuł:
Activation of Fms-like tyrosine kinase 3 signaling enhances survivin expression in a mouse model of rheumatoid arthritis.
Autorzy:
Andersson SE; Department of Rheumatology and Inflammation Research, Sahlgrenska University Hospital, University of Göteborg, Göteborg, Sweden. />Svensson MN
Erlandsson MC
Dehlin M
Andersson KM
Bokarewa MI
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Źródło:
PloS one [PLoS One] 2012; Vol. 7 (10), pp. e47668. Date of Electronic Publication: 2012 Oct 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Signal Transduction*/drug effects
Arthritis, Rheumatoid/*enzymology
Inhibitor of Apoptosis Proteins/*metabolism
Repressor Proteins/*metabolism
fms-Like Tyrosine Kinase 3/*metabolism
Adult ; Aged ; Aged, 80 and over ; Alternative Splicing/drug effects ; Alternative Splicing/genetics ; Animals ; Arthritis, Rheumatoid/pathology ; Bone Marrow/drug effects ; Bone Marrow/metabolism ; Disease Models, Animal ; Down-Regulation/drug effects ; Enzyme Activation/drug effects ; Female ; Humans ; Inhibitor of Apoptosis Proteins/genetics ; Male ; Membrane Proteins/pharmacology ; Mice ; Mice, Inbred BALB C ; Middle Aged ; RNA, Small Interfering/metabolism ; Repressor Proteins/genetics ; Spleen/drug effects ; Spleen/metabolism ; Survivin ; Up-Regulation/drug effects ; Young Adult ; fms-Like Tyrosine Kinase 3/antagonists & inhibitors
Czasopismo naukowe
Tytuł:
Src-Like adaptor protein (SLAP) binds to the receptor tyrosine kinase Flt3 and modulates receptor stability and downstream signaling.
Autorzy:
Kazi JU; Experimental Clinical Chemistry, Wallenberg Laboratory, Department of Laboratory Medicine, Lund University, Skåne University Hospital, Malmö, Sweden.
Rönnstrand L
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Źródło:
PloS one [PLoS One] 2012; Vol. 7 (12), pp. e53509. Date of Electronic Publication: 2012 Dec 31.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Neoplasms/*metabolism
Proto-Oncogene Proteins pp60(c-src)/*metabolism
Signal Transduction/*physiology
fms-Like Tyrosine Kinase 3/*metabolism
Animals ; COS Cells ; Cell Line ; Chlorocebus aethiops ; Humans ; Leukemia, Myeloid, Acute/genetics ; Leukemia, Myeloid, Acute/metabolism ; Mice ; Neoplasms/genetics ; Phosphorylation ; Proto-Oncogene Proteins pp60(c-src)/genetics ; Ubiquitination ; fms-Like Tyrosine Kinase 3/genetics
Czasopismo naukowe

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