The Elusive Chronic Myeloid Leukemia Stem Cell: Does It Matter and How Do We Eliminate It?

被引:22
作者
Carter, Bing Z. [1 ]
Mak, Duncan H. [1 ]
Cortes, Jorge [2 ]
Andreeff, Michael [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Sect Mol Hematol & Therapy, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
CHRONIC MYELOGENOUS LEUKEMIA; TOXIN-INTERLEUKIN-3 FUSION PROTEIN; BCR-ABL; IMATINIB MESYLATE; BLAST-CRISIS; TARGETED THERAPIES; INITIATING CELLS; CML CELLS; IN-VITRO; RESISTANCE;
D O I
10.1053/j.seminhematol.2010.06.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic myeloid leukemia (CML) is a clonal multistep myeloproliferative disease originating from and ultimately sustained by a rare population of BCR-ABL(+) cells with multilineage stem cell properties. Imatinib, the most successful of molecular targeted therapies, has revolutionized treatment of patients with CML. Despite this achievement, CML is often not curable, largely due to the innate insensitivity of CML stem cells, particularly when in a quiescent state. This failure of not only imatinib but also the second-generation tyrosine kinase inhibitors (TKIs) frequently leads to relapse upon drug discontinuation. Thus, any curative therapy must eliminate CML stern cells. A comprehensive understanding of the biological properties of CML stem cells and an elucidation of the molecular mechanisms and signaling pathways enabling these CML stem cells to self-renew, combined with insight into the regulation of apoptosis signaling and the mechanisms governing the interaction of CML stem cells with their bone marrow microenvironment, will facilitate the development of therapies for targeting these cells. Here, we discuss the biological properties of CML stem cells and potential strategies to eliminate them. Semin Hematol 47:362-370. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:362 / 370
页数:9
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