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急性白血病中克隆性与转化的关系。

Relationship between clonality and transformation in acute leukemia.

作者信息

Butturini A, Gale R P

机构信息

Department of Pediatrics, University of Parma, Italy.

出版信息

Leuk Res. 1991;15(1):1-7. doi: 10.1016/0145-2126(91)90137-i.

Abstract

In some cases of acute leukemia an initial potentially leukemogenic genetic alteration can result in clonally derived end-cells normal in appearance and numbers. We refer to this clonal expansion as preleukemia. Subsequent alterations, intrinsic or extrinsic, often referred to as transformation, result in abnormal differentiation and/or growth regulation; we refer to this as leukemia. Several issues are unresolved. Where in the hierarchy of hematopoiesis clonal expansion and transformation occur is unknown. It is quite likely that clonal expansion occurs in cells with considerable self-renewal potential--probably stem or progenitor cells. The precise site may vary in different cases and account for the diverse phenotypes of acute leukemia. How the preleukemia clone comes to dominate hematopoiesis and the fate of the residual normal stem cells and their progeny are also unknown. Likewise, there is controversy whether different models of leukemogenesis operate in different subjects. For example, are older persons or those with occupational exposure to potentially leukomogenic agents more likely to exhibit one pattern of leukomogenesis? Finally, it is unknown whether these diverse models of leukemogenesis respond differently to therapy.

摘要

在某些急性白血病病例中,最初潜在的致白血病基因改变可导致克隆衍生的终末细胞在外观和数量上正常。我们将这种克隆性扩增称为白血病前期。随后的改变,无论是内在的还是外在的,通常称为转化,会导致异常分化和/或生长调节;我们将此称为白血病。有几个问题尚未解决。克隆性扩增和转化发生在造血层级的何处尚不清楚。很可能克隆性扩增发生在具有相当自我更新潜能的细胞中——可能是干细胞或祖细胞。确切位置在不同病例中可能有所不同,并解释了急性白血病的多样表型。白血病前期克隆如何开始主导造血以及残余正常干细胞及其后代的命运也不清楚。同样,关于不同的白血病发生模型是否在不同个体中起作用也存在争议。例如,老年人或职业接触潜在致白血病因子的人是否更有可能表现出一种白血病发生模式?最后,尚不清楚这些不同的白血病发生模型对治疗的反应是否不同。

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