IDH1突变通过ALKBH2影响DNA修复,使胶质母细胞瘤细胞对青蒿素敏感。

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Olivier Switzeny, Stefan Pusch, Markus Christmann, Bernd Kaina
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引用次数: 0

摘要

背景:异柠檬酸脱氢酶1和2 (IDH1和IDH2)是催化异柠檬酸氧化脱羧成α-酮戊二酸(α-KG)的酶,这在许多代谢过程中是必需的,包括DNA修复的一些步骤。在肿瘤中,尤其是在胶质瘤中,IDH1和IDH2经常发生突变。在不同的癌症中发现的突变在功能上是活跃的,导致2-羟基戊二酸酯(2-HG)的形成而不是α-KG,其抑制α-KG依赖性酶。携带突变IDH1/2的胶质瘤比相同级别的IDH1野生型(wt)肿瘤预后更好,这可能是DNA修复功能受到抑制的结果。依赖于α-KG的DNA修复酶是alkB同源物2 (ALKBH2),它可以从DNA中去除一些损伤。这些发现促使我们研究胶质瘤细胞对青蒿琥酯(ART)的反应,ART是一种具有遗传毒性和抗癌活性的植物成分,目前已在几项试验中使用。材料和方法:我们使用表达IDH1野生型或基于tet诱导系统的IDH1突变(mt)蛋白的等基因胶质母细胞瘤细胞系,并用增加剂量的青蒿琥酯处理它们。我们还用2-HG处理胶质母细胞瘤细胞,产生ALKBH2敲除细胞,并检查它们对青蒿琥酯细胞毒性作用的敏感性。结果:我们发现在胶质母细胞瘤细胞中表达IDH1突变体(R132H)可以增强ART的细胞杀伤作用。此外,我们发现2-HG可以模拟IDH1mt的作用,因为2-HG可以改善ART的细胞毒性。最后,我们证明敲除ALKBH2会导致胶质母细胞瘤细胞对ART的敏感化。结论:这些数据表明,ALKBH2可以抑制ART的抗癌作用,低级别胶质瘤中常见的IDH1/2突变通过ALKBH2依赖性机制对ART增敏。这些数据支持在治疗idh1 /2突变的癌症中使用ART联合化疗和辅助治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IDH1 Mutation Impacts DNA Repair Through ALKBH2 Rendering Glioblastoma Cells Sensitive to Artesunate.

Background: Isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) are enzymes that catalyze the oxidative decarboxylation of isocitrate to alpha-ketoglutarate (α-KG), which is essential for many metabolic processes, including some steps in DNA repair. In tumors, notably in gliomas, IDH1 and IDH2 are frequently mutated. The mutation found in different cancers is functionally active, causing, instead of α-KG, the formation of 2-hydroxyglutarate (2-HG), which inhibits α-KG-dependent enzymes. Gliomas harboring mutated IDH1/2 show a better prognosis than IDH1 wild-type (wt) tumors of the same grade, which might result from the inhibition of DNA repair functions. A DNA repair enzyme dependent on α-KG is alkB homolog 2 (ALKBH2), which removes several lesions from DNA. These findings prompted us to investigate the response of glioma cells to artesunate (ART), a plant ingredient with genotoxic and anticancer activity currently used in several trials. Materials and Methods: We used isogenic glioblastoma cell lines that express IDH1 wild-type or, based on a TET-inducible system, the IDH1 mutant (mt) protein, and treated them with increasing doses of artesunate. We also treated glioblastoma cells with 2-HG, generated ALKBH2 knockout cells, and checked their sensitivity to the cytotoxic effects of artesunate. Results: We show that the cell-killing effect of ART is enhanced if the IDH1 mutant (R132H) is expressed in glioblastoma cells. Further, we show that 2-HG imitates the effect of IDH1mt as 2-HG ameliorates the cytotoxicity of ART. Finally, we demonstrate that the knockout of ALKBH2 causes the sensitization of glioblastoma cells to ART. Conclusions: The data indicate that ALKBH2 protects against the anticancer effect of ART, and the mutation of IDH1/2 commonly occurring in low-grade gliomas sensitizes to ART via an ALKBH2-dependent mechanism. The data support the use of ART in the therapy of IDH1/2-mutated cancers both in combination with chemotherapy and adjuvant treatment.

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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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