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http://purl.uniprot.org/citations/18818703http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18818703http://www.w3.org/2000/01/rdf-schema#comment"Philadelphia chromosome-positive (Ph(+)) chronic myeloid leukemia (CML) induced by the BCR-ABL oncogene is believed to be developed from leukemic stem cells (LSCs), and we have previously shown in mice that LSCs for CML express the same cell surface markers that are also expressed on normal hematopoietic stem cells (HSCs). Although the inhibition of BCR-ABL kinase activity by imatinib is highly effective in treating human Ph(+) CML in chronic phase, it is difficult to achieve molecular remission of the disease, suggesting that LSCs remain in patients. In this study, we find that following imatinib treatment, LSCs not only remained but also accumulated increasingly in bone marrow of CML mice. This insensitivity of LSCs to imatinib was not because of the lack of BCR-ABL kinase inhibition by imatinib, and proliferating leukemic cells derived from LSCs were still sensitive to growth inhibition by imatinib. These results identify an LSC survival pathway that is not inhibited by imatinib. Furthermore, we show that beta-catenin in the Wnt signaling pathway is essential for survival and self-renewal of LSCs, providing a new strategy for targeting these cells."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.org/dc/terms/identifier"doi:10.1038/leu.2008.262"xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/author"Chen Y."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/author"Hu Y."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/author"Li S."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/author"Douglas L."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/name"Leukemia"xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/pages"109-116"xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/title"beta-Catenin is essential for survival of leukemic stem cells insensitive to kinase inhibition in mice with BCR-ABL-induced chronic myeloid leukemia."xsd:string
http://purl.uniprot.org/citations/18818703http://purl.uniprot.org/core/volume"23"xsd:string
http://purl.uniprot.org/citations/18818703http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18818703
http://purl.uniprot.org/citations/18818703http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18818703
http://purl.uniprot.org/uniprot/#_Q02248-mappedCitation-18818703http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18818703
http://purl.uniprot.org/uniprot/#_Q3UZT7-mappedCitation-18818703http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18818703
http://purl.uniprot.org/uniprot/#_Q80VE7-mappedCitation-18818703http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18818703
http://purl.uniprot.org/uniprot/Q02248http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18818703
http://purl.uniprot.org/uniprot/Q80VE7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18818703
http://purl.uniprot.org/uniprot/Q3UZT7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18818703