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替莫唑胺引起的组蛋白甲基化;一种经典的DNA甲基化抗癌药物。

Histone Methylation by Temozolomide; A Classic DNA Methylating Anticancer Drug.

作者信息

Wang Tieli, Pickard Amanda J, Gallo James M

机构信息

Department of Chemistry and Biochemistry, California State University Dominguez Hills, Carson, CA, U.S.A.

Department of Pharmacology and Systems Therapeutics, Icahn School of Medicine at Mount Sinai, New York, NY, U.S.A.

出版信息

Anticancer Res. 2016 Jul;36(7):3289-99.

Abstract

BACKGROUND/AIM: The alkylating agent, temozolomide (TMZ), is considered the standard-of-care for high-grade astrocytomas -known as glioblastoma multiforme (GBM)- an aggressive type of tumor with poor prognosis. The therapeutic benefit of TMZ is attributed to formation of DNA adducts involving the methylation of purine bases in DNA. We investigated the effects of TMZ on arginine and lysine amino acids, histone H3 peptides and histone H3 proteins.

MATERIALS AND METHODS

Chemical modification of amino acids, histone H3 peptide and protein by TMZ was performed in phosphate buffer at physiological pH. The reaction products were examined by mass spectrometry and western blot analysis.

RESULTS

Our results showed that TMZ following conversion to a methylating cation, can methylate histone H3 peptide and histone H3 protein, suggesting that TMZ exerts its anticancer activity not only through its interaction with DNA, but also through alterations of protein post-translational modifications.

CONCLUSION

The possibility that TMZ can methylate histones involved with epigenetic regulation of protein indicates a potentially unique mechanism of action. The study will contribute to the understanding the anticancer activity of TMZ in order to develop novel targeted molecular strategies to advance the cancer treatment.

摘要

背景/目的:烷化剂替莫唑胺(TMZ)被认为是高级别星形细胞瘤(即多形性胶质母细胞瘤,GBM)的标准治疗药物,GBM是一种侵袭性肿瘤,预后较差。TMZ的治疗益处归因于DNA加合物的形成,其中涉及DNA中嘌呤碱基的甲基化。我们研究了TMZ对精氨酸和赖氨酸氨基酸、组蛋白H3肽和组蛋白H3蛋白的影响。

材料与方法

在生理pH值的磷酸盐缓冲液中,TMZ对氨基酸、组蛋白H3肽和蛋白质进行化学修饰。通过质谱和蛋白质印迹分析检测反应产物。

结果

我们的结果表明,TMZ转化为甲基化阳离子后,可以使组蛋白H3肽和组蛋白H3蛋白甲基化,这表明TMZ不仅通过与DNA相互作用发挥抗癌活性,还通过改变蛋白质的翻译后修饰发挥作用。

结论

TMZ可使参与蛋白质表观遗传调控的组蛋白甲基化,这一可能性表明其具有潜在独特的作用机制。该研究将有助于理解TMZ的抗癌活性,以便开发新的靶向分子策略来推进癌症治疗。

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