期刊
BRITISH JOURNAL OF CANCER
卷 102, 期 10, 页码 1474-1482出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6605670
关键词
PBOX; CML; T315I; Bcr-Abl; apoptosis
类别
资金
- Science Foundation Ireland
- Cancer Research Ireland
BACKGROUND: Imatinib is a direct and potent inhibitor of the constitutively active tyrosine kinase, breakpoint cluster region-Abelson (Bcr-Abl), which is central to the pathogenesis of chronic myeloid leukaemia (CML) patients. As such, imatinib has become the frontline treatment for CML patients. However, the recent emergence of imatinib resistance, commonly associated with point mutations within the kinase domain, has led to the search for alternative drug treatments and combination therapies for CML. METHODS: In this report, we analyse the effects of representative members of the novel pro-apoptotic microtubule depolymerising pyrrolo-1,5-benzoxazepines or PBOX compounds on chemotherapy-refractory CML cells using a series of Bcr-Abl mutant cell lines, clinical ex vivo patient samples and an in vivo mouse model. RESULTS: The PBOX compounds potently reduce cell viability in cells expressing the E225K and H396P mutants as well as the highly resistant T315I mutant. The PBOX compounds also induce apoptosis in primary CML samples including those resistant to imatinib. We also show for the first time, the in vivo efficacy of the pro-apoptotic PBOX compound, PBOX-6, in a CML mouse model of the T315I Bcr-Abl mutant. CONCLUSION: Results from this study highlight the potential of these novel series of PBOX compounds as an effective therapy against CML. British Journal of Cancer (2010) 102, 1474-1482. doi:10.1038/sj.bjc.6605670 www.bjcancer.com Published online 20 April 2010 (C) 2010 Cancer Research UK
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