Insights into the stem cells of chronic myeloid leukemia

被引:92
作者
Sloma, I. [1 ]
Jiang, X. [1 ]
Eaves, A. C. [1 ]
Eaves, C. J. [1 ]
机构
[1] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
关键词
chronic myeloid leukemia; leukemic stem cell; cancer stem cell; genomic instability; self-renewal; CHRONIC MYELOGENOUS LEUKEMIA; HEMATOPOIETIC PROGENITOR CELLS; BCR-ABL GENE; BLAST-CRISIS CML; COMPLETE CYTOGENETIC RESPONSE; BONE-MARROW-TRANSPLANTATION; CHRONIC MYELOCYTIC-LEUKEMIA; TERM REPOPULATING ACTIVITY; COLONY-STIMULATING FACTOR; KINASE DOMAIN MUTATIONS;
D O I
10.1038/leu.2010.159
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic myeloid leukemia (CML) has long served as a paradigm for generating new insights into the cellular origin, pathogenesis and improved approaches to treating many types of human cancer. Early studies of the cellular phenotypes and genotypes represented in leukemic populations obtained from CML patients established the concept of an evolving clonal disorder originating in and initially sustained by a rare, multipotent, self-maintaining hematopoietic stem cell (HSC). More recent investigations continue to support this model, while also revealing new insights into the cellular and molecular mechanisms that explain how knowledge of CML stem cells and their early differentiating progeny can predict the differing and variable features of chronic phase and blast crisis. In particular, these emphasize the need for new agents that effectively and specifically target CML stem cells to produce non-toxic, but curative therapies that do not require lifelong treatments. Leukemia (2010) 24, 1823-1833; doi:10.1038/leu.2010.159; published online 23 September 2010
引用
收藏
页码:1823 / 1833
页数:11
相关论文
共 132 条
[1]   Glycogen synthase kinase 3β missplicing contributes to leukemia stem cell generation [J].
Abrahamsson, Annelie E. ;
Geron, Ifat ;
Gotlib, Jason ;
Dao, Kim-Hien T. ;
Barroga, Charlene F. ;
Newton, Isabel G. ;
Giles, Francis J. ;
Durocher, Jeffrey ;
Creusot, Remi S. ;
Karimi, Mobin ;
Jones, Carol ;
Zehnder, James L. ;
Keating, Armand ;
Negrin, Robert S. ;
Weissman, Irving L. ;
Jamieson, Catriona H. M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (10) :3925-3929
[2]   LYMPHOID BLAST CRISES OF CHRONIC MYELOGENOUS LEUKEMIA REPRESENT STAGES IN THE DEVELOPMENT OF B-CELL PRECURSORS [J].
BAKHSHI, A ;
MINOWADA, J ;
ARNOLD, A ;
COSSMAN, J ;
JENSEN, JP ;
WHANGPENG, J ;
WALDMANN, TA ;
KORSMEYER, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (14) :826-831
[3]   Modeling the initiation and progression of human acute leukemia in mice [J].
Barabe, Frederic ;
Kennedy, James A. ;
Hope, Kristin J. ;
Dick, John E. .
SCIENCE, 2007, 316 (5824) :600-604
[4]   Bcr-Abl expression levels determine the rate of development of resistance to imatinib mesylate in chronic myeloid leukemia [J].
Barnes, DJ ;
Palaiologou, D ;
Panousopoulou, E ;
Schultheis, B ;
Yong, ASM ;
Wong, A ;
Pattacini, L ;
Goldman, JM ;
Melo, JV .
CANCER RESEARCH, 2005, 65 (19) :8912-8919
[5]  
BEDI A, 1993, BLOOD, V81, P2898
[6]   Targeting autophagy potentiates tyrosine kinase inhibitor-induced cell death in Philadelphia chromosome-positive cells, including primary CML stem cells [J].
Bellodi, Cristian ;
Lidonnici, Maria Rosa ;
Hamilton, Ashley ;
Helgason, G. Vignir ;
Soliera, Angela Rachele ;
Ronchetti, Mattia ;
Galavotti, Sara ;
Young, Kenneth W. ;
Selmi, Tommaso ;
Yacobi, Rinat ;
Van Etten, Richard A. ;
Donato, Nick ;
Hunter, Ann ;
Dinsdale, David ;
Tirro, Elena ;
Vigneri, Paolo ;
Nicotera, Pierluigi ;
Dyer, Martin J. ;
Holyoake, Tessa ;
Salomoni, Paolo ;
Calabretta, Bruno .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (05) :1109-1123
[7]  
BIERNAUX C, 1995, BLOOD, V86, P3118
[8]  
Bonifazi F, 2001, BLOOD, V98, p348A
[9]   The presence of typical and atypical BCR-ABL fusion genes in leukocytes of normal individuals: Biologic significance and implications for the assessment of minimal residual disease [J].
Bose, S ;
Deininger, M ;
Gora-Tybor, J ;
Goldman, JM ;
Melo, JV .
BLOOD, 1998, 92 (09) :3362-3367
[10]  
Brain JM, 2003, CANCER RES, V63, P4895