Source:http://linkedlifedata.com/resource/pubmed/id/16001089
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0018956,
umls-concept:C0023473,
umls-concept:C0026336,
umls-concept:C0185117,
umls-concept:C0242643,
umls-concept:C0332161,
umls-concept:C0591833,
umls-concept:C0871261,
umls-concept:C0935989,
umls-concept:C1517945,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911684,
umls-concept:C2911692
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pubmed:issue |
9
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pubmed:dateCreated |
2005-8-24
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pubmed:abstractText |
Selective inhibition of the BCR/ABL tyrosine kinase by imatinib has become a first-line therapy for chronic myelogenous leukemia (CML). However, BCR/ABL-positive progenitors often persist despite treatment, and relapse associated with resistance to imatinib has been described in many patients with advanced disease. Drug efflux by P-glycoprotein (P-gp), as well as point mutations in BCR/ABL oncoprotein, has been implicated in the mechanism of resistance to imatinib. In this study, we established a murine transplantation model of CML-like myeloproliferative disease using Mdr1a/1b-null mice and analyzed the effects of loss of P-gp on resistance to imatinib. We found that mice transplanted with Mdr1a/1b-null bone marrow (BM) that had been transduced with a BCR/ABL retroviral vector displayed similar responses to imatinib, compared with those transplanted with BCR/ABL-transduced wild-type BM. In the absence of P-gp, the incidence and latency of disease in secondary recipients was not changed in imatinib-treated mice, relative to wild-type controls. Furthermore, K562 cells engineered to overexpress P-gp remained sensitive to imatinib-induced growth inhibition and cell death. Together, our findings suggest that P-gp expression in hematopoietic stem cells does not significantly contribute to imatinib resistance in CML.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0887-6924
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1590-6
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:16001089-Animals,
pubmed-meshheading:16001089-Bone Marrow Transplantation,
pubmed-meshheading:16001089-Cell Survival,
pubmed-meshheading:16001089-Cell Transplantation,
pubmed-meshheading:16001089-Disease Models, Animal,
pubmed-meshheading:16001089-Drug Resistance, Neoplasm,
pubmed-meshheading:16001089-Hematopoietic Stem Cells,
pubmed-meshheading:16001089-Humans,
pubmed-meshheading:16001089-K562 Cells,
pubmed-meshheading:16001089-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:16001089-Mice,
pubmed-meshheading:16001089-Mice, Knockout,
pubmed-meshheading:16001089-P-Glycoprotein,
pubmed-meshheading:16001089-Piperazines,
pubmed-meshheading:16001089-Pyrimidines,
pubmed-meshheading:16001089-Survival Analysis
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pubmed:year |
2005
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pubmed:articleTitle |
Loss of P-glycoprotein expression in hematopoietic stem cells does not improve responses to imatinib in a murine model of chronic myelogenous leukemia.
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pubmed:affiliation |
Division of Experimental Hematology, Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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