The potential role of COVID-19 in the induction of DNA damage

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Reviews in Mutation Research Pub Date : 2022-01-01 DOI:10.1016/j.mrrev.2022.108411
Pablo Pánico, Patricia Ostrosky-Wegman, Ana María Salazar
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引用次数: 15

Abstract

The coronavirus disease-2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is challenging global health and economic systems. In some individuals, COVID-19 can cause a wide array of symptoms, affecting several organs, such as the lungs, heart, bowels, kidneys and brain, causing multiorgan failure, sepsis and death. These effects are related in part to direct viral infection of these organs, immunological deregulation, a hypercoagulatory state and the potential for development of cytokine storm syndrome. Since the appearance of COVID-19 is recent, the long-term effects on the health of recovered patients remain unknown. In this review, we focused on current evidence of the mechanisms of DNA damage mediated by coronaviruses. Data supports that these viruses can induce DNA damage, genomic instability, and cell cycle deregulation during their replication in mammalian cells. Since the induction of DNA damage and aberrant DNA repair mechanisms are related to the development of chronic diseases such as cancer, diabetes, neurodegenerative disorders, and atherosclerosis, it will be important to address similar effects and outcomes in recovered COVID-19 patients.

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COVID-19在诱导DNA损伤中的潜在作用
由严重急性呼吸系统综合征冠状病毒-2 (SARS-CoV-2)引起的冠状病毒病-2019 (COVID-19)正在挑战全球卫生和经济系统。在一些人身上,COVID-19可引起广泛的症状,影响几个器官,如肺、心脏、肠道、肾脏和大脑,导致多器官衰竭、败血症和死亡。这些影响部分与这些器官的直接病毒感染、免疫失调、高凝状态和细胞因子风暴综合征的发展潜力有关。由于COVID-19是最近出现的,因此对康复患者健康的长期影响尚不清楚。在这篇综述中,我们重点介绍了目前冠状病毒介导的DNA损伤机制的证据。数据支持这些病毒在哺乳动物细胞中复制时可诱导DNA损伤、基因组不稳定和细胞周期失调。由于DNA损伤的诱导和异常的DNA修复机制与癌症、糖尿病、神经退行性疾病和动脉粥样硬化等慢性疾病的发展有关,因此在康复的COVID-19患者中解决类似的效果和结果将非常重要。
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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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