Xiucheng Pan, Fulong Zhang, Hongjuan You, Lihong Ma, Xing Wang, Yiran Han, Jiaqi Yao, Kuiyang Zheng, Fanyun Kong, Renxian Tang
Journal: Frontiers in cellular and infection microbiology 2022;12():1062553
PMID: 36506030
DEAD/H-box helicases are an essential protein family with a conserved motif containing unique amino acid sequences (Asp-Glu-Ala-Asp/His). Current evidence indicates that DEAD/H-box helicases regulate RNA metabolism and innate immune responses. In recent years, DEAD/H-box helicases have been reported to participate in the development of a variety of diseases, including hepatitis B virus (HBV) infection, which is a significant risk factor for hepatic fibrosis, cirrhosis, and liver cancer. Furthermore, emerging evidence suggests that different DEAD/H-box helicases play vital roles in the regulation of viral replication, based on the interaction of DEAD/H-box helicases with HBV and the modulation of innate signaling pathways mediated by DEAD/H-box helicases. Besides these, HBV can alter the expression and activity of DEAD/H-box helicases to facilitate its biosynthesis. More importantly, current investigation suggests that targeting DEAD/H-box helicases with appropriate compounds is an attractive treatment strategy for the virus infection. In this review, we delineate recent advances in molecular mechanisms relevant to the interplay of DEAD/H-box helicase and HBV and the potential of targeting DEAD/H-box helicase to eliminate HBV infection.
Copyright © 2022 You, Ma, Wang, Zhang, Han, Yao, Pan, Zheng, Kong and Tang.
© Copyright 2026, Nutrition Evidence
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