磷脂代谢适应促进IDH2突变型急性髓系白血病细胞的存活。

IF 4.5 2区 医学 Q1 ONCOLOGY Cancer Science Pub Date : 2023-10-26 DOI:10.1111/cas.15994
Tatsuya Morishima, Koichi Takahashi, Desmond Wai Loon Chin, Yuxin Wang, Kenji Tokunaga, Yuichiro Arima, Masao Matsuoka, Toshio Suda, Hitoshi Takizawa
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引用次数: 0

摘要

在急性髓细胞白血病(AML)患者中检测到异柠檬酸脱氢酶(IDH)基因的遗传突变,其导致产生肿瘤代谢产物的病理酶活性。虽然已经开发出靶向突变IDH酶并使细胞内癌代谢产物水平正常化的特异性抑制剂,但仍有难治性和耐药性的报道。由于病理性酶活性的获得伴随着IDH突变细胞中关键的WT IDH酶活性的消除,因此即使在细胞内癌代谢产物水平正常化之后,IDH突变体细胞中的异常代谢也可能持续存在。具有和不具有IDH2基因突变的等基因AML细胞系的比较揭示了IDH2突变细胞生长优势的两个相互排斥的信号,与细胞内癌代谢产物水平相关的STAT磷酸化和磷脂代谢适应。后者在肿瘤代谢产物正常化后被发现,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。美国食品药品监督管理局批准的针对花生四烯酸代谢的抗炎药释放这种代谢适应可以使IDH2突变细胞对凋亡敏感,从而在体外和体内根除它们。我们的发现将有助于开发IDH2突变AML患者的替代治疗方案,这些患者对目前可用的治疗方法不耐受。
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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Phospholipid metabolic adaptation promotes survival of IDH2 mutant acute myeloid leukemia cells

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.

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来源期刊
Cancer Science
Cancer Science 医学-肿瘤学
自引率
3.50%
发文量
406
审稿时长
2 months
期刊介绍: Cancer Science (formerly Japanese Journal of Cancer Research) is a monthly publication of the Japanese Cancer Association. First published in 1907, the Journal continues to publish original articles, editorials, and letters to the editor, describing original research in the fields of basic, translational and clinical cancer research. The Journal also accepts reports and case reports. Cancer Science aims to present highly significant and timely findings that have a significant clinical impact on oncologists or that may alter the disease concept of a tumor. The Journal will not publish case reports that describe a rare tumor or condition without new findings to be added to previous reports; combination of different tumors without new suggestive findings for oncological research; remarkable effect of already known treatments without suggestive data to explain the exceptional result. Review articles may also be published.
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Issue Information In this issue Issue Information In this issue Real-world genome profiling in Japanese patients with pancreatic ductal adenocarcinoma focusing on HRD implications
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