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pubmed-article:15850831pubmed:abstractTextImatinib mesylate is a novel tyrosine kinase inhibitor used for the treatment of Philadelphia chromosome positive (Ph+) leukemia and other malignancies. In previous studies, we found significant telomere shortening in Ph+ cells from patients with chronic myeloid leukemia (CML). Interestingly, imatinib treatment was found to lead to a normalization of previously shortened telomere length in CML patients. Based on recent reports demonstrating that c-ABL phosphorylates hTERT and thereby inhibits hTERT activity, a direct effect of imatinib on hTERT activity leading to telomere elongation in BCR-ABL-positive cells has been proposed by others. Such an effect could be of potential importance for telomere maintenance in Ph+ cells by facilitating clonal selection and progression of the disease to blast crisis.lld:pubmed
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pubmed-article:15850831pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15850831pubmed:articleTitleTelomere length and telomerase activity in the BCR-ABL-transformed murine Pro-B cell line BaF3 is unaffected by treatment with imatinib.lld:pubmed
pubmed-article:15850831pubmed:affiliationDepartment of Hematology and Oncology, University of Tübingen, Tübingen, Germany.lld:pubmed
pubmed-article:15850831pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15850831pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed