共 89 条
Therapeutic targets in chronic myeloid leukaemia
被引:25
作者:

Heaney, Nicholas B.
论文数: 0 引用数: 0
h-index: 0
机构:
Royal Infirm, ATMU & Canc Div, Sect Expt Haematol & Haemopoiet Stem Cells, Glasgow G31 2ER, Lanark, Scotland Royal Infirm, ATMU & Canc Div, Sect Expt Haematol & Haemopoiet Stem Cells, Glasgow G31 2ER, Lanark, Scotland

Holyoake, Tessa L.
论文数: 0 引用数: 0
h-index: 0
机构:
Royal Infirm, ATMU & Canc Div, Sect Expt Haematol & Haemopoiet Stem Cells, Glasgow G31 2ER, Lanark, Scotland Royal Infirm, ATMU & Canc Div, Sect Expt Haematol & Haemopoiet Stem Cells, Glasgow G31 2ER, Lanark, Scotland
机构:
[1] Royal Infirm, ATMU & Canc Div, Sect Expt Haematol & Haemopoiet Stem Cells, Glasgow G31 2ER, Lanark, Scotland
关键词:
chronic myeloid leukaemia;
bcr-abl;
haemopoietic stem cell;
drug therapy;
imatinib mesylate;
tyrosine kinase inhibitors;
imatinib resistance;
D O I:
10.1002/hon.813
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chronic myeloid leukaemia (CML) is a clonal disorder of the haemopoietic stem cell arising as a consequence of the formation of the bcr-abl oncogene. The particular molecular basis of this condition has enabled the development of therapies that selectively target diseased cells. The success of the rationally designed first-line therapy imatinib mesylate (IM) is tempered by the problems of disease persistence and resistance. Novel strategies have been identified to take forward therapy in CML and these will be discussed in this review. This work is generated from a review of published literature and contains particular insight into the work performed by our group in this field. Copyright (c) 2007 John Wiley & Sons, Ltd.
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页码:66 / 75
页数:10
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

Garcia-Manero, G
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

Giles, F
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

Faderl, S
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

Sugrue, M
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA

Cortes, J
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机构: Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[10]
Comparison of imatinib, mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen:: high efficacy of drug combinations
[J].
Bradeen, Heather A.
;
Eide, Christopher A.
;
O'Hare, Thomas
;
Johnson, Kara J.
;
Willis, Stephanie G.
;
Lee, Francis Y.
;
Druker, Brian J.
;
Deininger, Michael W.
.
BLOOD,
2006, 108 (07)
:2332-2338

Bradeen, Heather A.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Eide, Christopher A.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

O'Hare, Thomas
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Johnson, Kara J.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Willis, Stephanie G.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Lee, Francis Y.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Druker, Brian J.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA

Deininger, Michael W.
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机构: Oregon Hlth & Sci Univ, Inst Canc, Portland, OR 97239 USA