醛诱导的 DNA 蛋白交联--DNA 损伤、修复和诱变

IF 3.5 3区 医学 Q2 ONCOLOGY
Thomas Blouin, Natalie Saini
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引用次数: 0

摘要

研究表明,接触醛会导致 DNA 损伤的形成,包括 DNA 蛋白交联(DPC)、碱基加合物以及链间或链内交联。由于最近在检测和量化这些加合物方面取得的进展,DPCs 最近引起了更多关注。DPC 对基因组的稳定性具有极大的破坏性,已被证明会阻断复制叉,导致大范围的突变。防止 DPC 引起的损伤的细胞机制包括切除修复途径、同源重组以及参与将共价结合的蛋白质从 DNA 中清除的专门蛋白酶。这些途径最早是在经甲醛处理的细胞中发现的,但自那时起,其他各种醛类物质也被证明可诱导细胞中 DPC 的形成。DPC 修复或醛清除机制的缺陷会导致各种疾病,包括人类的 Ruijs-Aalfs 综合征和 AMeD 综合征。在这里,我们将讨论在了解醛如何形成 DPCs、如何修复 DPCs 以及这些修复途径缺陷的后果方面的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aldehyde-induced DNA-protein crosslinks- DNA damage, repair and mutagenesis
Aldehyde exposure has been shown to lead to the formation of DNA damage comprising of DNA-protein crosslinks (DPCs), base adducts and interstrand or intrastrand crosslinks. DPCs have recently drawn more attention because of recent advances in detection and quantification of these adducts. DPCs are highly deleterious to genome stability and have been shown to block replication forks, leading to wide-spread mutagenesis. Cellular mechanisms to prevent DPC-induced damage include excision repair pathways, homologous recombination, and specialized proteases involved in cleaving the covalently bound proteins from DNA. These pathways were first discovered in formaldehyde-treated cells, however, since then, various other aldehydes have been shown to induce formation of DPCs in cells. Defects in DPC repair or aldehyde clearance mechanisms lead to various diseases including Ruijs-Aalfs syndrome and AMeD syndrome in humans. Here, we discuss recent developments in understanding how aldehydes form DPCs, how they are repaired, and the consequences of defects in these repair pathways.
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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