烷基二钴胺光介导的双链DNA切割

IF 3.261
Liberty N. Gendron , Jennifer R. Shell , Thomas A. Shell
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引用次数: 1

摘要

通过自由基形成导致DNA双链断裂(DSBs)的药物已被证明对治疗癌症有效,因为DSBs导致细胞凋亡。几十年来,人们一直对治疗癌症的光反应剂感兴趣,因为它们能够通过控制照明区域来控制化学反应,从而限制其影响。与维生素B12 (B12)结构相关的烷基钴胺在绿光(约530 nm)照射下产生的自由基量子产率非常高。癌细胞比健康细胞摄取烷基钴胺的程度更大,因为这些快速分裂的细胞对B12的需求增加。用丙基拴住两个钴胺导致一个复合物,以光介导的方式引起真正的DNA dsb。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Light-mediated double-strand DNA cleavage by an alkyldicobalamin

Light-mediated double-strand DNA cleavage by an alkyldicobalamin

Agents that cause double-strand breaks (DSBs) of DNA via radical formation have been demonstrated to be effective in treating cancer because DSBs result in cellular apoptosis. Light-responsive agents for the treatment of cancer have been of interest for decades because they afford the ability to spatially control chemical reactions limiting the effects by controlling the area of illumination. Alkylcobalamins, which are structurally related to Vitamin B12 (B12), produce radicals with very high quantum yields when illuminated with green light (approximately 530 nm). Cancerous cells uptake alkylcobalamins to a greater extent than healthy cells because these rapidly dividing cells have an increased demand for B12. Tethering two cobalamins with a propyl group results in a complex that causes true DNA DSBs in a light-mediated manner.

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