Is lineage decision-making restricted during tumoral reprograming of haematopoietic stem cells?

被引:8
|
作者
Brown, Geoffrey [1 ]
Sanchez-Garcia, Isidro [2 ,3 ]
机构
[1] Univ Birmingham, Coll Med & Dent Sci, Sch Immun & Infect, Birmingham, W Midlands, England
[2] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, Expt Therapeut & Translat Oncol Program, E-37008 Salamanca, Spain
[3] Inst Biomed Res Salamanca IBSAL, Salamanca, Spain
关键词
haematopoiesis; leukemia; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; T-CELL; PROGENITOR CELLS; STEM/PROGENITOR CELLS; RECURRENT MUTATIONS; MYELOID-LEUKEMIA; CLONAL EVOLUTION; DNMT3A MUTATIONS; RECEPTOR-GAMMA;
D O I
10.18632/oncotarget.6145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Within the past years there have been substantial changes to our understanding of haematopoiesis and cells that initiate and sustain leukemia. Recent studies have revealed that developing haematopoietic stem and progenitor cells are much more heterogeneous and versatile than has been previously thought. This versatility includes cells using more than one route to a fate and cells having progressed some way towards a cell type retaining other lineage options as clandestine. These notions impact substantially on our understanding of the origin and nature of leukemia. An important question is whether leukemia stem cells are as versatile as their cell of origin as an abundance of cells belonging to a lineage is often a feature of overt leukemia. In this regard, we examine the coming of age of the "leukemia stem cell" theory and the notion that leukemia, like normal haematopoiesis, is a hierarchically organized tissue. We examine evidence to support the notion that whilst cells that initiate leukemia have multi-lineage potential, leukemia stem cells are reprogrammed by further oncogenic insults to restrict their lineage decision-making. Accordingly, evolution of a sub-clone of lineage-restricted malignant cells is a key feature of overt leukemia.
引用
收藏
页码:43326 / 43341
页数:16
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