Recent advances in acute myeloid leukemia stem cell biology

被引:109
作者
Horton, Sarah J. [1 ,2 ]
Huntly, Brian J. P. [1 ,2 ,3 ]
机构
[1] Univ Cambridge, Dept Haematol, Cambridge Inst Med Res, Cambridge, England
[2] Cambridge Stem Cell Initiat, Cambridge, England
[3] Cambridge Univ Fdn Hosp Trust, Cambridge, England
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 07期
基金
英国惠康基金; 英国医学研究理事会;
关键词
acute myeloid leukemia; leukemic stem cells; cellular; molecular; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; INITIATING CELLS; MELANOMA-CELLS; GEMTUZUMAB OZOGAMICIN; EXPRESSION SIGNATURE; CLONAL EVOLUTION; SELF-RENEWAL; MLL-ENL; TARGET;
D O I
10.3324/haematol.2011.054734
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The existence of cancer stem cells has long been postulated, but was proven less than 20 years ago following the demonstration that only a small sub-fraction of leukemic cells from acute myeloid leukemia patients were able to propagate the disease in xenografts. These cells were termed leukemic stem cells since they exist at the apex of a loose hierarchy, possess extensive self-renewal and the ability to undergo limited differentiation into leukemic blasts. Acute myeloid leukemia is a heterogeneous condition at both the phenotypic and molecular level with a variety of distinct genetic alterations giving rise to the disease. Recent studies have highlighted that this heterogeneity extends to the leukemic stem cell, with this dynamic compartment evolving to overcome various selection pressures imposed upon it during disease progression. The result is a complex situation in which multiple pools of leukemic stem cells may exist within individual patients which differ both phenotypically and molecularly. Since leukemic stem cells are thought to be resistant to current chemotherapeutic regimens and mediate disease relapse, their study also has potentially profound clinical implications. Numerous studies have generated important recent advances in the field, including the identification of novel leukemic stem cell-specific cell surface antigens and gene expression signatures. These tools will no doubt prove invaluable for the rational design of targeted therapies in the future.
引用
收藏
页码:966 / 974
页数:9
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