Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, FC, Italy.
Leukemia. 2019 Jul;33(7):1543-1556. doi: 10.1038/s41375-019-0490-0. Epub 2019 May 24.
Chronic myeloid leukemia (CML) is caused by BCRABL1 in a cell with the biological potential, intrinsic or acquired, to cause leukemia. This cell is commonly termed the CML leukemia stem cell (LSC). In humans a CML LSC is operationally-defined by ≥1 in vitro or in vivo assays of human leukemia cells transferred to immune-deficient mice. Results of these assays are sometimes discordant. There is also the unproved assumption that biological features of a CML LSC are stable. These considerations make accurate and precise identification of a CML LSC difficult or impossible. In this review, we consider biological features of CML LSCs defined by these assays. We also consider whether CML LSCs are susceptible to targeting by tyrosine kinase inhibitors (TKIs) and other drugs, and whether elimination of CML LSCs is needed to achieve therapy-free remission or cure CML.
慢性髓性白血病(CML)是由具有引起白血病的生物学潜能(内在或获得的)的细胞中的 BCRABL1 引起的。这种细胞通常被称为 CML 白血病干细胞(LSC)。在人类中,CML LSC 通过≥1 种体外或体内实验来操作定义,即将人类白血病细胞转移到免疫缺陷小鼠中。这些实验的结果有时并不一致。此外,还有一个未经证实的假设,即 CML LSC 的生物学特征是稳定的。这些考虑因素使得准确和精确地识别 CML LSC 变得困难或不可能。在这篇综述中,我们考虑了这些实验定义的 CML LSC 的生物学特征。我们还考虑了 CML LSCs 是否容易受到酪氨酸激酶抑制剂(TKIs)和其他药物的靶向作用,以及是否需要消除 CML LSCs 才能实现无治疗缓解或治愈 CML。