接触工程纳米材料如何影响我们的表观遗传密码?机制及分子靶点研究进展

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Luciana Moreira , Carla Costa , Joana Pires , João Paulo Teixeira , Sónia Fraga
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引用次数: 7

摘要

有证据表明,工程纳米材料(ENM)可以诱导表观遗传修饰。在这篇综述中,我们概述了ENM诱导基因表达的表观遗传调控在各种应用中的应用:二氧化钛(TiO2)、银(Ag)、金(Au)、二氧化硅(SiO2)纳米粒子和碳基纳米材料(CNM)。暴露于这些ENM可引发DNA甲基化、转录后组蛋白修饰和非编码RNA表达的细胞模式改变。这种效应取决于ENM的剂量和物理化学性质,包括大小、形状和表面化学,以及细胞/生物体的敏感性。受影响的基因主要涉及表观遗传机制本身的调控,以及细胞凋亡、细胞周期、DNA修复和炎症相关通路,这些通路的长期改变可能导致某些病理的发生或进展。此外,一些DNA甲基化模式可能作为表观遗传记忆的一种形式被保留。产前暴露于ENM可能会通过经胎盘作用和/或印记基因的推定传递损害后代的正常发育。因此,了解ENM对表观基因组的影响至关重要,在评估ENM对人类健康的风险时,必须考虑表观遗传评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How can exposure to engineered nanomaterials influence our epigenetic code? A review of the mechanisms and molecular targets

Evidence suggests that engineered nanomaterials (ENM) can induce epigenetic modifications. In this review, we provide an overview of the epigenetic modulation of gene expression induced by ENM used in a variety of applications: titanium dioxide (TiO2), silver (Ag), gold (Au), silica (SiO2) nanoparticles and carbon-based nanomaterials (CNM). Exposure to these ENM can trigger alterations in cell patterns of DNA methylation, post-transcriptional histone modifications and expression of non-coding RNA. Such effects are dependent on ENM dose and physicochemical properties including size, shape and surface chemistry, as well as on the cell/organism sensitivity. The genes affected are mostly involved in the regulation of the epigenetic machinery itself, as well as in apoptosis, cell cycle, DNA repair and inflammation related pathways, whose long-term alterations might lead to the onset or progression of certain pathologies. In addition, some DNA methylation patterns may be retained as a form of epigenetic memory. Prenatal exposure to ENM may impair the normal development of the offspring by transplacental effects and/or putative transmission of epimutations in imprinting genes. Thus, understanding the impact of ENM on the epigenome is of paramount importance and epigenetic evaluation must be considered when assessing the risk of ENM to human health.

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来源期刊
CiteScore
12.20
自引率
1.90%
发文量
22
审稿时长
15.7 weeks
期刊介绍: The subject areas of Reviews in Mutation Research encompass the entire spectrum of the science of mutation research and its applications, with particular emphasis on the relationship between mutation and disease. Thus this section will cover advances in human genome research (including evolving technologies for mutation detection and functional genomics) with applications in clinical genetics, gene therapy and health risk assessment for environmental agents of concern.
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