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通过DNA双链断裂的高通量检测鉴定化学诱导的DNA损伤

Chemical-Induced DNA Damage Identification by High-Throughput Detection of DNA Double-Strand Break.

作者信息

Sunada Shigeaki

机构信息

Juntendo Advanced Research Institute for Health Science, Juntendo University, Bunkyo-ku, Tokyo, Japan.

出版信息

Methods Mol Biol. 2025;2933:113-117. doi: 10.1007/978-1-0716-4574-1_15.

Abstract

Numerous chemicals cause diverse types of DNA damage in cells. However, the failure of DNA repair associated with the formation of these lesions converts the diverse forms of DNA damage into the more severe form of damage, the DNA double-strand break (DSB). The DSB is also considered an early factor in the carcinogenic process. Therefore, analytical methods for detecting DSBs can contribute to the detection of carcinogenic chemicals. γH2AX has been widely used as a highly sensitive marker for DSB, and analytical methods using flow cytometry have excellent quantitative properties. I further attempted to simplify and expedite the method while maintaining its quantitative performance and established a high-throughput DSB quantification method. In this section, I present a simple method for evaluating the DNA damage potential of chemicals in terms of DSB formation.

摘要

许多化学物质会在细胞中导致多种类型的DNA损伤。然而,与这些损伤形成相关的DNA修复失败会将多种形式的DNA损伤转化为更严重的损伤形式——DNA双链断裂(DSB)。DSB也被认为是致癌过程中的一个早期因素。因此,检测DSB的分析方法有助于检测致癌化学物质。γH2AX已被广泛用作DSB的高灵敏度标志物,并且使用流式细胞术的分析方法具有出色的定量特性。我进一步尝试在保持其定量性能的同时简化和加快该方法,并建立了一种高通量DSB定量方法。在本节中,我将介绍一种根据DSB形成来评估化学物质DNA损伤潜力的简单方法。

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