The molecular pathogenesis of acute myeloid leukemia

被引:58
|
作者
Steffen, B [1 ]
Müller-Tidow, C [1 ]
Schwäble, J [1 ]
Berdel, WE [1 ]
Serve, H [1 ]
机构
[1] Univ Munster, Dept Med Hematol Oncol, D-48129 Munster, Germany
关键词
AML; signal transduction; transcription factor; Flt3; Wnt; AML1-ETO; tyrosine kinase;
D O I
10.1016/j.critrevonc.2004.10.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The description of the molecular pathogenesis of acute myeloid leukemias (AML) has seen dramatic progress over the last years. Two major types of genetic events have been described that are crucial for leukemic transformation: alterations in myeloid transcription factors governing hematopoietic differentiation and activating mutations of signal transduction intermediates. These processes are highly interdependent, since the molecular events changing the transcriptional control in hematopoietic progenitor cells modify the composition of signal transduction molecules available for growth factor receptors, while the activating mutations in signal transduction molecules induce alterations in the activity and expression of several transcription factors that are crucial for normal myeloid differentiation. The purpose of this article is to review the current literature describing these genetic events, their biological consequences and their clinical implications. As the article will show, the recent description of several critical transforming mutations in AML may soon give rise to more efficient and less toxic molecularly targeted therapies of this deadly disease. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:195 / 221
页数:27
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