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- W3089969311 abstract "Dengue virus (DENV) is a mosquito-borne pathogen that threatens 2.5 billion people in more than 100 countries annually. Dengue infection induces a spectrum of clinical symptoms, ranging from classical dengue fever to severe dengue hemorrhagic fever or dengue shock syndrome; however, the complexities of DENV immunopathogenesis remain controversial. Previous studies have reported the importance of the transcription factor Nrf2 in the control of redox homeostasis and antiviral/inflammatory or death responses to DENV. Importantly, the production of reactive oxygen species and the subsequent stress response have been linked to the development of inflammation and progression toward the more severe forms of the disease. Here, we demonstrate that DENV uses the NS2B3 protease complex to strategically target Nrf2 for degradation, leading to a progressive increase in oxidative stress, inflammation, and cell death in infected cells. This study underlines the pivotal role of the Nrf2 regulatory network in the context of DENV infection." @default.
- W3089969311 created "2020-10-08" @default.
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- W3089969311 date "2020-11-23" @default.
- W3089969311 modified "2023-10-06" @default.
- W3089969311 title "Dengue Virus Targets Nrf2 for NS2B3-Mediated Degradation Leading to Enhanced Oxidative Stress and Viral Replication" @default.
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- W3089969311 doi "https://doi.org/10.1128/jvi.01551-20" @default.
- W3089969311 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7925186" @default.
- W3089969311 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32999020" @default.
- W3089969311 hasPublicationYear "2020" @default.
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