Nakahara Fumio, Weiss Cary N, Ito Keisuke
Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Departments of Cell Biology and Medicine, Albert Einstein Cancer Center, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Int J Hematol. 2014 Jul;100(1):18-26. doi: 10.1007/s12185-014-1518-x. Epub 2014 Feb 1.
The tumor suppressor promyelocytic leukemia (PML) was first identified as a component of PML-RARα fusion protein, one of the initiating cytogenetic abnormalities in acute promyelocytic leukemia. PML is now known to have diverse functions regulating the DNA-damage response, apoptosis, senescence, and angiogenesis. Recent investigations have identified PML as a regulator of metabolic pathways in stem cell compartments, including the hematopoietic system, and have provided researchers with new strategies for controlling stem cell maintenance and differentiation. Studies of PML in leukemia-initiating cells demonstrate that PML is also an essential component of their maintenance, which has drawn tremendous attention to PML from scientists in various stem cell fields. Here, we review research into PML and its associated pathways, including recent studies of PML as it relates to stem cell biology, as well as our finding that PML regulates fatty acid oxidation, which is essential to the maintenance of normal hematopoietic stem cells. We also discuss the therapeutic potential of controlling PML-associated pathways. In particular, we describe promising evidence for the use of arsenic trioxide in the treatment of chronic myeloid leukemia.
肿瘤抑制因子早幼粒细胞白血病(PML)最初被鉴定为PML-RARα融合蛋白的一个组成部分,该融合蛋白是急性早幼粒细胞白血病起始细胞遗传学异常之一。现在已知PML具有多种功能,可调节DNA损伤反应、细胞凋亡、衰老和血管生成。最近的研究已确定PML是包括造血系统在内的干细胞区室中代谢途径的调节因子,并为研究人员提供了控制干细胞维持和分化的新策略。对白血病起始细胞中PML的研究表明,PML也是其维持的重要组成部分,这引起了各个干细胞领域科学家对PML的极大关注。在此,我们综述了对PML及其相关途径的研究,包括最近关于PML与干细胞生物学关系的研究,以及我们发现PML调节脂肪酸氧化,这对维持正常造血干细胞至关重要。我们还讨论了控制PML相关途径的治疗潜力。特别是,我们描述了三氧化二砷用于治疗慢性髓性白血病的有前景的证据。