Momparler Richard L, Côté Sylvie, Momparler Louise F
Département de pharmacologie-physiologie, Université de Montréal, Montréal, QC H3C 3J7, Canada.
Service d'hématologie-oncologie, Centre de recherche, CHU Sainte-Justine, Montreal, QC H3T 1C5, Canada.
Epigenomes. 2020 Mar 1;4(1):3. doi: 10.3390/epigenomes4010003.
Most patients with acute myeloid leukemia (AML) have a poor prognosis. Curative therapy of AML requires the complete eradication of the leukemic stem cells (LSCs). One aspect of LSCs that is poorly understood is their low frequency in the total population of leukemic cells in AML patients. After each cell division of LSCs, most of the daughter cells lose their capacity for self-renewal. Investigations into the role of Isocitrate dehydrogenase (IDH) mutations in AML provide some insight on the regulation of the proliferation of LSCs. The primary role of IDH is to convert isocitrate to alpha-keto-glutarate (α-KG). When IDH is mutated, it converts α-KG to 2-hydroxyglutarate (2-HG), an inhibitor of the TET pathway and Jumonji-C histone demethylases (JHDMs). The demethylating action of these enzymes removes the epigenetic gene-silencing markers, DNA methylation, H3K27me3 and H3K9me2 and can lead to the differentiation of LSCs. This enzymatic action is blocked by 2-HG in mutated IDH (mut-IDH) AML patients, who can be induced into remission with antagonists of 2-HG. These observations suggest that there exists in cells a natural enzymatic mechanism that uses demethylation to reverse epigenetic gene-silencing, leading to a loss of the self-renewal capacity of LSCs. This mechanism limits the proliferative potential of LSCs. Epigenetic agents that inhibit DNA and histone methylation exhibit a synergistic antineoplastic action on AML cells. It is possible that the therapeutic potential of this epigenetic therapy may be enhanced by demethylation enzymes, resulting in a very effective treatment for AML.
大多数急性髓系白血病(AML)患者预后较差。AML的根治性治疗需要彻底清除白血病干细胞(LSCs)。LSCs的一个尚未被充分理解的方面是它们在AML患者白血病细胞总数中的低频率。LSCs每次细胞分裂后,大多数子细胞会失去自我更新能力。对异柠檬酸脱氢酶(IDH)突变在AML中的作用的研究为LSCs增殖的调控提供了一些见解。IDH的主要作用是将异柠檬酸转化为α-酮戊二酸(α-KG)。当IDH发生突变时,它会将α-KG转化为2-羟基戊二酸(2-HG),这是一种TET途径和Jumonji-C组蛋白去甲基化酶(JHDMs)的抑制剂。这些酶的去甲基化作用会去除表观遗传基因沉默标记、DNA甲基化、H3K27me3和H3K9me2,并可导致LSCs分化。在突变IDH(mut-IDH)AML患者中,这种酶促作用被2-HG阻断,这些患者可以用2-HG拮抗剂诱导缓解。这些观察结果表明,细胞中存在一种天然的酶促机制,该机制利用去甲基化来逆转表观遗传基因沉默,导致LSCs自我更新能力丧失。这种机制限制了LSCs的增殖潜力。抑制DNA和组蛋白甲基化的表观遗传药物对AML细胞具有协同抗肿瘤作用。这种表观遗传疗法的治疗潜力可能通过去甲基化酶得到增强,从而产生一种非常有效的AML治疗方法。