Determination of Phosphorylated Histone H2AX in Nanoparticle-Induced Genotoxic Studies.
Determination of Phosphorylated Histone H2AX in Nanoparticle-Induced Genotoxic Studies.
复制标题
纳米颗粒诱导的基因毒性研究中磷酸化组蛋白 H2AX 的测定。
DOI:
10.1007/978-1-4939-8916-4_9
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发表时间:
2019
期刊:
影响因子:
--
通讯作者:
Zhang,Qunwei
中科院分区:
文献类型:
--
作者:
Wan,Rong;Mo,Yiqun;Tong,Ruirui;Gao,Meiqin;Zhang,Qunwei
DNA double-strand breaks (DSBs), one of the most severe lesions of DNA damage triggered by various genotoxic insults, can lead to chromosome change, genomic instability, and even tumorigenesis if not repaired efficiently. In response to DNA damage, histone H2AX molecules are rapidly phosphorylated at serine 139 near the site of DNA DSBs and form γ-H2AX foci. As an early important cellular event linked to DNA damage and repair, γ-H2AX is a highly sensitive biomarker for “monitoring” DNA damage and consequently is a useful tool in genetic toxicology screen. We and other researchers have used γ-H2AX as a marker to assess the potential genotoxic effects of some nanoparticles in vitro and in vivo. In this chapter, we describe several useful methods for γ-H2AX detection, which can be used to evaluate the potential genotoxic effects of nanoparticles.