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磷脂代谢适应性促进 IDH2 突变型急性髓系白血病细胞的存活。

Phospholipid metabolic adaptation promotes survival of IDH2 mutant acute myeloid leukemia cells.

机构信息

Laboratory of Stem Cell Stress, International Research Center for Medical Sciences (IRCMS), Kumamoto University, Kumamoto, Japan.

Laboratory of Hematopoietic Stem Cell Engineering, IRCMS, Kumamoto University, Kumamoto, Japan.

出版信息

Cancer Sci. 2024 Jan;115(1):197-210. doi: 10.1111/cas.15994. Epub 2023 Oct 26.

Abstract

Genetic mutations in the isocitrate dehydrogenase (IDH) gene that result in a pathological enzymatic activity to produce oncometabolite have been detected in acute myeloid leukemia (AML) patients. While specific inhibitors that target mutant IDH enzymes and normalize intracellular oncometabolite level have been developed, refractoriness and resistance has been reported. Since acquisition of pathological enzymatic activity is accompanied by the abrogation of the crucial WT IDH enzymatic activity in IDH mutant cells, aberrant metabolism in IDH mutant cells can potentially persist even after the normalization of intracellular oncometabolite level. Comparisons of isogenic AML cell lines with and without IDH2 gene mutations revealed two mutually exclusive signalings for growth advantage of IDH2 mutant cells, STAT phosphorylation associated with intracellular oncometabolite level and phospholipid metabolic adaptation. The latter came to light after the oncometabolite normalization and increased the resistance of IDH2 mutant cells to arachidonic acid-mediated apoptosis. The release of this metabolic adaptation by FDA-approved anti-inflammatory drugs targeting the metabolism of arachidonic acid could sensitize IDH2 mutant cells to apoptosis, resulting in their eradication in vitro and in vivo. Our findings will contribute to the development of alternative therapeutic options for IDH2 mutant AML patients who do not tolerate currently available therapies.

摘要

在急性髓系白血病(AML)患者中已经检测到异柠檬酸脱氢酶(IDH)基因突变,这些突变导致病理性酶活性产生致癌代谢物。虽然已经开发出针对突变 IDH 酶并使细胞内致癌代谢物水平正常化的特定抑制剂,但已经报道了耐药性和抗性。由于获得病理性酶活性伴随着突变 IDH 细胞中关键 WT IDH 酶活性的丧失,因此即使在细胞内致癌代谢物水平正常化后,突变 IDH 细胞中的异常代谢仍可能持续存在。对具有和不具有 IDH2 基因突变的同基因 AML 细胞系进行比较,揭示了 IDH2 突变细胞生长优势的两种相互排斥的信号通路,与细胞内致癌代谢物水平相关的 STAT 磷酸化和磷脂代谢适应。在致癌代谢物正常化后,后者变得明显,并增加了 IDH2 突变细胞对花生四烯酸介导的细胞凋亡的抗性。通过针对花生四烯酸代谢的 FDA 批准的抗炎药物释放这种代谢适应,可以使 IDH2 突变细胞对细胞凋亡敏感,从而在体外和体内消除它们。我们的发现将有助于为不能耐受现有治疗方法的 IDH2 突变 AML 患者开发替代治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e895/10823289/3ffafcb571d4/CAS-115-197-g001.jpg

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