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利用显微镜原位检测复杂DNA损伤:前路崎岖。

In Situ Detection of Complex DNA Damage Using Microscopy: A Rough Road Ahead.

作者信息

Nikitaki Zacharenia, Pariset Eloise, Sudar Damir, Costes Sylvain V, Georgakilas Alexandros G

机构信息

Physics Department, School of Applied Mathematical and Physical Sciences, DNA Damage Laboratory, National Technical University of Athens (NTUA), 15780 Zografou, Athens, Greece.

Space Biosciences Division, Radiation Biophysics Laboratory, NASA Ames Research Center, Moffett Field, CA 94035, USA.

出版信息

Cancers (Basel). 2020 Nov 6;12(11):3288. doi: 10.3390/cancers12113288.

Abstract

Complexity of DNA damage is considered currently one if not the primary instigator of biological responses and determinant of short and long-term effects in organisms and their offspring. In this review, we focus on the detection of complex (clustered) DNA damage (CDD) induced for example by ionizing radiation (IR) and in some cases by high oxidative stress. We perform a short historical perspective in the field, emphasizing the microscopy-based techniques and methodologies for the detection of CDD at the cellular level. We extend this analysis on the pertaining methodology of surrogate protein markers of CDD (foci) colocalization and provide a unique synthesis of imaging parameters, software, and different types of microscopy used. Last but not least, we critically discuss the main advances and necessary future direction for the better detection of CDD, with important outcomes in biological and clinical setups.

摘要

目前,DNA损伤的复杂性被认为是生物反应的主要引发因素之一,也是生物体及其后代短期和长期影响的决定因素。在本综述中,我们聚焦于例如由电离辐射(IR)以及在某些情况下由高氧化应激诱导的复杂(簇状)DNA损伤(CDD)的检测。我们对该领域进行了简短的历史回顾,重点介绍了基于显微镜的技术和在细胞水平检测CDD的方法。我们将此分析扩展到CDD(病灶)共定位的替代蛋白标志物的相关方法,并对成像参数、软件和所使用的不同类型显微镜进行了独特的综合介绍。最后但同样重要的是,我们批判性地讨论了更好地检测CDD的主要进展和必要的未来方向,这些进展在生物学和临床环境中具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7a0/7694657/32dc936b9eb6/cancers-12-03288-g001.jpg

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