Aldehyde Dehydrogenase Enzyme Functions in Acute Leukemia Stem Cells.

Garrett M Dancik, Ioannis F Voutsas, Spiros Vlahopoulos
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引用次数: 4

Abstract

The enzymes that belong to the aldehyde dehydrogenase family are expressed in a variety of cells; yet activity of their main members characterizes stem cells, both normal and malignant. Several members of this family perform critical functions in stem cells, in general, and a few have been shown to have key roles in malignant tumors and their recurrence. In particular, ALDH1A1, which localizes to the cytosol and the nucleus, is an enzyme critical in cancer stem cells. In acute myeloid leukemia (AML), ALDH1A1 protects leukemia-initiating cells from a number of antineoplastic agents, and proves vital for the establishment of human AML xenografts in mice. ALDH2, which is located in mitochondria, has a major role in alcohol metabolism by clearing ethanol-derived acetaldehyde. Haematopoietic stem cells require ALDH2 for protection against acetaldehyde, which can cause damage to DNA, leading to insertions, deletions, chromosomal rearrangements, and translocations. Mutations compromise stem cell function, and thereby threaten blood homeostasis. We review here the potential of targeting the enzymatic activity of aldehyde dehydrogenases in acute leukemia.

醛脱氢酶在急性白血病干细胞中的作用。
醛脱氢酶家族的酶在多种细胞中表达;然而,它们的主要成员的活动是干细胞的特征,无论是正常的还是恶性的。一般来说,这个家族的几个成员在干细胞中发挥关键作用,其中一些已被证明在恶性肿瘤及其复发中起关键作用。特别是定位于细胞质和细胞核的ALDH1A1,是癌症干细胞中至关重要的酶。在急性髓性白血病(AML)中,ALDH1A1保护白血病起始细胞免受许多抗肿瘤药物的影响,并证明了在小鼠中建立人类AML异种移植物的重要作用。ALDH2位于线粒体中,通过清除乙醇衍生的乙醛在酒精代谢中起主要作用。造血干细胞需要ALDH2来保护其免受乙醛的侵害,乙醛会导致DNA损伤,导致插入、缺失、染色体重排和易位。突变损害干细胞功能,从而威胁血液稳态。本文综述了靶向急性白血病中乙醛脱氢酶活性的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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