Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-8-27
pubmed:abstractText
Acute myeloid leukemia (AML) is maintained by rare leukemia-initiating cells (L-ICs). FLT3 and/or PI3K pathways are often dysregulated in AML and may be important for L-IC survival. The presence of PI3K pathway intermediate integrin linked kinase (ILK), and FLT3 was confirmed in five L-IC-enriched AML patient samples. Treatment of AML cells with QLT0267, an inhibitor of ILK and FLT3, decreased survival of long-term suspension culture-initiating cells and NOD/SCID mouse L-IC. In contrast, little toxicity toward normal bone marrow progenitors was observed, demonstrating that candidate leukemic stem cells can be eliminated by inhibition of these targets while normal hematopoietic counterparts are spared.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Azo Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Cytarabine, http://linkedlifedata.com/resource/pubmed/chemical/Daunorubicin, http://linkedlifedata.com/resource/pubmed/chemical/FLT3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Glycogen Synthase Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Pyrazoles, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering, http://linkedlifedata.com/resource/pubmed/chemical/fms-Like Tyrosine Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/integrin-linked kinase
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1873-5835
pubmed:author
pubmed:copyrightInfo
Copyright (c) 2010 Elsevier Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1358-65
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:20193963-Adult, pubmed-meshheading:20193963-Aged, pubmed-meshheading:20193963-Animals, pubmed-meshheading:20193963-Azo Compounds, pubmed-meshheading:20193963-Cells, Cultured, pubmed-meshheading:20193963-Cytarabine, pubmed-meshheading:20193963-Daunorubicin, pubmed-meshheading:20193963-Female, pubmed-meshheading:20193963-Glycogen Synthase Kinase 3, pubmed-meshheading:20193963-Humans, pubmed-meshheading:20193963-Leukemia, Myeloid, Acute, pubmed-meshheading:20193963-Male, pubmed-meshheading:20193963-Mice, pubmed-meshheading:20193963-Mice, Inbred NOD, pubmed-meshheading:20193963-Middle Aged, pubmed-meshheading:20193963-Neoplastic Stem Cells, pubmed-meshheading:20193963-Phosphatidylinositol 3-Kinases, pubmed-meshheading:20193963-Phosphorylation, pubmed-meshheading:20193963-Protein Kinase Inhibitors, pubmed-meshheading:20193963-Protein-Serine-Threonine Kinases, pubmed-meshheading:20193963-Pyrazoles, pubmed-meshheading:20193963-RNA, Small Interfering, pubmed-meshheading:20193963-Stem Cells, pubmed-meshheading:20193963-fms-Like Tyrosine Kinase 3
pubmed:year
2010
pubmed:articleTitle
Targeting integrin linked kinase and FMS-like tyrosine kinase-3 is cytotoxic to acute myeloid leukemia stem cells but spares normal progenitors.
pubmed:affiliation
Terry Fox Laboratory, British Columbia Cancer Research Centre, Vancouver, BC, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't