Cited 115 time in
Therapeutic Modulation of Virus-Induced Oxidative Stress via the Nrf2-Dependent Antioxidative Pathway
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Choongho | - |
| dc.date.accessioned | 2023-04-28T10:41:07Z | - |
| dc.date.available | 2023-04-28T10:41:07Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.issn | 1942-0900 | - |
| dc.identifier.issn | 1942-0994 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/9977 | - |
| dc.description.abstract | Virus-induced oxidative stress plays a critical role in the viral life cycle as well as the pathogenesis of viral diseases. In response to reactive oxygen species (ROS) generation by a virus, a host cell activates an antioxidative defense system for its own protection. Particularly, a nuclear factor erythroid 2p45-related factor 2 (Nrf2) pathway works in a front-line for cytoprotection and detoxification. Recently, a series of studies suggested that a group of clinically relevant viruses have the capacity for positive and negative regulations of the Nrf2 pathway. This virus-induced modulation of the host antioxidative response turned out to be a crucial determinant for the progression of several viral diseases. In this review, virus-specific examples of positive and negative modulations of the Nrf2 pathway will be summarized first. Then a number of successful genetic and pharmacological manipulations of the Nrf2 pathway for suppression of the viral replication and the pathogenesis-associated oxidative damage will be discussed later. Understanding of the interplay between virus-induced oxidative stress and antioxidative host response will aid in the discovery of potential antiviral supplements for better management of viral diseases. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | HINDAWI LTD | - |
| dc.title | Therapeutic Modulation of Virus-Induced Oxidative Stress via the Nrf2-Dependent Antioxidative Pathway | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1155/2018/6208067 | - |
| dc.identifier.scopusid | 2-s2.0-85058038859 | - |
| dc.identifier.wosid | 000449794600001 | - |
| dc.identifier.bibliographicCitation | OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, v.2018 | - |
| dc.citation.title | OXIDATIVE MEDICINE AND CELLULAR LONGEVITY | - |
| dc.citation.volume | 2018 | - |
| dc.type.docType | Review | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Cell Biology | - |
| dc.relation.journalWebOfScienceCategory | Cell Biology | - |
| dc.subject.keywordPlus | HEPATITIS-C VIRUS | - |
| dc.subject.keywordPlus | RESPIRATORY SYNCYTIAL VIRUS | - |
| dc.subject.keywordPlus | REGULATING HEME OXYGENASE-1 | - |
| dc.subject.keywordPlus | FACTOR E2-RELATED FACTOR-2 | - |
| dc.subject.keywordPlus | PORCINE CIRCOVIRUS TYPE-2 | - |
| dc.subject.keywordPlus | KAPPA-B ACTIVATION | - |
| dc.subject.keywordPlus | GENE-EXPRESSION | - |
| dc.subject.keywordPlus | UP-REGULATION | - |
| dc.subject.keywordPlus | EPITHELIAL-CELLS | - |
| dc.subject.keywordPlus | NRF2 ACTIVATION | - |
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