Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/25751
DC Field | Value | |
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dc.title | In vivo activity of ABT-869, a multi-target kinase inhibitor, against acute myeloid leukemia with wild-type FLT3 receptor | |
dc.contributor.author | Zhou, J. | |
dc.contributor.author | Khng, J. | |
dc.contributor.author | Jasinghe, V.J. | |
dc.contributor.author | Bi, C. | |
dc.contributor.author | Poon, L.F. | |
dc.contributor.author | Xie, Z. | |
dc.contributor.author | Chen, C.-S. | |
dc.contributor.author | Neo, C.H.S. | |
dc.contributor.author | Pan, M. | |
dc.contributor.author | Yu, H. | |
dc.contributor.author | Yeoh, A.E.-J. | |
dc.contributor.author | Lu, Y. | |
dc.contributor.author | Glaser, K.B. | |
dc.contributor.author | Albert, D.H. | |
dc.contributor.author | Davidsen, S.K. | |
dc.date.accessioned | 2011-08-16T07:52:39Z | |
dc.date.available | 2011-08-16T07:52:39Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | Zhou, J., Khng, J., Jasinghe, V.J., Bi, C., Poon, L.F., Xie, Z., Chen, C.-S., Neo, C.H.S., Pan, M., Yu, H., Yeoh, A.E.-J., Lu, Y., Glaser, K.B., Albert, D.H., Davidsen, S.K. (2008). In vivo activity of ABT-869, a multi-target kinase inhibitor, against acute myeloid leukemia with wild-type FLT3 receptor. Leukemia Research 32 (7) : 1091-1100. ScholarBank@NUS Repository. | |
dc.identifier.issn | 01452126 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/25751 | |
dc.description.abstract | Neoangiogenesis plays an important role in leukemogenesis. We investigated the in vivo anti-leukemic effect of ABT-869 against AML with wild-type FLT3 using RFP transfected HL60 cells with in vivo imaging technology on both the subcutaneous and systemic leukemia xenograft models. ABT-869 showed a five-fold inhibition of tumor growth in comparison with vehicle control. IHC analysis revealed that ABT-869 decreased p-VEGFR1, Ki-67 labeling index, VEGF and remarkably increased apoptotic cells in the xenograft models. ABT-869 also reduced the leukemia burden and prolonged survival. Our study supports the rationale for clinically testing an anti-angiogenesis agent in AML with wild-type FLT3. © 2007 Elsevier Ltd. All rights reserved. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.leukres.2007.11.025 | |
dc.source | Scopus | |
dc.subject | Acute myeloid leukemia | |
dc.subject | In vivo | |
dc.subject | Tyrosine kinase inhibitor | |
dc.subject | Whole-body imaging technology | |
dc.subject | Wild-type FLT3 receptor | |
dc.type | Article | |
dc.contributor.department | MEDICINE | |
dc.contributor.department | PHYSIOLOGY | |
dc.contributor.department | PAEDIATRICS | |
dc.description.sourcetitle | Leukemia Research | |
dc.description.volume | 32 | |
dc.description.issue | 7 | |
dc.description.page | 1091-1100 | |
dc.identifier.isiut | 000255856000013 | |
Appears in Collections: | Staff Publications |
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