Zhou Jianbiao, Chng Wee-Joo
Jianbiao Zhou, Wee-Joo Chng, Cancer Science Institute of Singapore, National University of Singapore, Centre for Translational Medicine, Singapore 117599, Singapore.
World J Stem Cells. 2014 Sep 26;6(4):473-84. doi: 10.4252/wjsc.v6.i4.473.
Accumulating evidence support the notion that acute myeloid leukemia (AML) is organized in a hierarchical system, originating from a special proportion of leukemia stem cells (LSC). Similar to their normal counterpart, hematopoietic stem cells (HSC), LSC possess self-renewal capacity and are responsible for the continued growth and proliferation of the bulk of leukemia cells in the blood and bone marrow. It is believed that LSC are also the root cause for the treatment failure and relapse of AML because LSC are often resistant to chemotherapy. In the past decade, we have made significant advancement in identification and understanding the molecular biology of LSC, but it remains a daunting task to specifically targeting LSC, while sparing normal HSC. In this review, we will first provide a historical overview of the discovery of LSC, followed by a summary of identification and separation of LSC by either cell surface markers or functional assays. Next, the review will focus on the current, various strategies for eradicating LSC. Finally, we will highlight future directions and challenges ahead of our ultimate goal for the cure of AML by targeting LSC.
越来越多的证据支持这样一种观点,即急性髓系白血病(AML)是由一个分层系统构成的,起源于特定比例的白血病干细胞(LSC)。与它们的正常对应物造血干细胞(HSC)相似,LSC具有自我更新能力,并负责血液和骨髓中大量白血病细胞的持续生长和增殖。据信,LSC也是AML治疗失败和复发的根本原因,因为LSC通常对化疗具有抗性。在过去十年中,我们在识别和理解LSC的分子生物学方面取得了重大进展,但特异性靶向LSC同时保留正常HSC仍然是一项艰巨的任务。在这篇综述中,我们将首先对LSC的发现进行历史概述,然后总结通过细胞表面标志物或功能测定来识别和分离LSC的方法。接下来,综述将聚焦于当前根除LSC的各种策略。最后,我们将强调在通过靶向LSC实现治愈AML这一最终目标之前的未来方向和挑战。