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Published on: December 23, 2020
Roles of p53-Mediated Host-Virus Interaction in Coronavirus Infection
Xue Wang1, Yi Liu1, Kaiyuan Li1
1College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Abstract:
The emergence of the SARS-CoV-2 coronavirus has garnered global attention due to its highly pathogenic nature and the resulting health crisis and economic burden. Although drugs such as Remdesivir have been considered a potential cure by targeting the virus on its RNA polymerase, the high mutation rate and unique 3' to 5' exonuclease with proofreading function make it challenging to develop effective anti-coronavirus drugs. As a result, there is an increasing focus on host-virus interactions because coronaviruses trigger stress responses, cell cycle changes, apoptosis, autophagy, and the dysregulation of immune function and inflammation in host cells. The p53 tumor suppressor molecule is a critical regulator of cell signaling pathways, cellular stress responses, DNA repair, and apoptosis. However, viruses can activate or inhibit p53 during viral infections to enhance viral replication and spread. Given its pivotal role in cell physiology, p53 represents a potential target for anti-coronavirus drugs. This review aims to summarize the relationship between p53 and coronaviruses from various perspectives, to shed light on potential targets for antiviral drug development and vaccine design.
Insights
Coronaviruses, like SARS-CoV-2, challenge drug development due to rapid mutation. Targeting the host cell
Area of Science:
- Virology
- Molecular Biology
- Oncology
Background:
- SARS-CoV-2 poses significant global health and economic challenges.
- Existing antivirals face limitations due to coronavirus high mutation rates and proofreading mechanisms.
- Coronaviruses manipulate host cell processes, including stress responses, cell cycle, apoptosis, and immune function.
Purpose of the Study:
- To review the complex interactions between p53 and coronaviruses.
- To explore p53 as a potential therapeutic target for antiviral drug development and vaccine design against coronaviruses.
Main Methods:
- Comprehensive literature review of studies on coronavirus-host interactions.
- Analysis of the role of the p53 tumor suppressor in cellular responses to viral infections.
- Examination of p53's involvement in pathways affected by coronaviruses.
Main Results:
- Coronaviruses can modulate p53 activity to facilitate viral replication.
- p53 plays a crucial role in regulating cellular stress, DNA repair, and apoptosis, processes often hijacked by viruses.
- Understanding p53's dynamic interaction with coronaviruses is key to identifying therapeutic vulnerabilities.
Conclusions:
- The p53 tumor suppressor is a critical node in the host response to coronavirus infection.
- Targeting p53 offers a promising strategy for developing novel antiviral therapies and effective vaccine designs.
- Further research into p53-coronavirus interactions could unlock new avenues for combating viral diseases.
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