Next-generation sequencing approaches for the study of genome and epigenome toxicity induced by sulfur mustard

被引:0
|
作者
Yunes Panahi
Amir Fattahi
Fatemeh Zarei
Navid Ghasemzadeh
Abbas Mohammadpoor
Sina Abroon
Jafar Nouri Nojadeh
Mehran Khojastefard
Abolfazl Akbarzadeh
Tohid Ghasemnejad
机构
[1] Baqiyatallah University of Medical Sciences,Chemical Injuries Research Center, System Biology and Poisoning Institute
[2] Tabriz University of Medical Sciences,Department of Reproductive Biology, Faculty of Advanced Medical Sciences
[3] Royan Institute for Stem Cell Biology and Technology,Department of Stem Cells and Developmental Biology at Cell Science Research Center
[4] ACECR,Department of Biochemistry, Faculty of Medicine
[5] Shahid Sadoughi University of Medical Sciences,Cellular and Molecular Research Center
[6] Urmia University of Medical Sciences,Stem Cell Research Center (SCRC)
[7] Tabriz University of Medical Sciences,Department of Medical Genetic, Faculty of Medicine
[8] Tabriz University of Medical Sciences,Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences
[9] Tabriz University of Medical Sciences,undefined
来源
Archives of Toxicology | 2018年 / 92卷
关键词
Sulfur mustard; Genotoxicity; Epigenome toxicity; NGS;
D O I
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中图分类号
学科分类号
摘要
Sulfur mustard (SM) is an extensive nucleophilic and alkylating agent that targets different tissues. The genotoxic property of SM is the most threatening effect, because it is associated with detrimental inflammations and susceptibility to several kinds of cancer. Moreover, SM causes a wide variety of adverse effects on DNA which result in accumulation of DNA adducts, multiple mutations, aneuploidies, and epigenetic aberrations in the genome. However, these adverse effects are still not known well, possibly because no valid biomarkers have been developed for detecting them. The advent of next-generation sequencing (NGS) has provided opportunities for the characterization of these alterations with a higher level of molecular detail and cost-effectivity. The present review introduces NGS approaches for the detection of SM-induced DNA adducts, mutations, chromosomal structural variation, and epigenetic aberrations, and also comparing and contrasting them with regard to which might be most advantageous.
引用
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页码:3443 / 3457
页数:14
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