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Molecular Insights into the MAPK Cascade during Viral Infection: Potential Crosstalk between HCQ and HCQ Analogues. | LitMetric

AI Article Synopsis

  • * COVID-19 has severely affected millions globally, yet effective treatments remain limited, leading to some countries testing controversial options like hydroxychloroquine (HCQ).
  • * This review aims to explore the MAPK cascade's involvement in viral infections and suggest potential therapeutic uses of MAPK inhibitors, highlighting the need for molecular understanding to develop new treatments for current and future pandemics.

Article Abstract

The mitogen-activated protein kinase (MAPK) pathway links the cell-surface receptors to the transcription machinery, transducing the extracellular signals into several outputs, which may also adapt the host defense mechanism to viral attacks. The Severe Acute Respiratory Syndrome CoronaVirus 2 (SARS-CoV-2) that causes the COrona VIrus Disease 2019 (COVID-19) has infected upwards of nearly 70 million people and worldwide has claimed more than 1,600,000 deaths. So far, there continues to be no specific treatment for this novel coronavirus-induced disease. In the search to control the global COVID-19 pandemic, some eastern and developing countries have approved a variety of treatments with controversial efficacy, among which is the use of the antimalarial hydroxychloroquine (HCQ). Interestingly, prior data had indicated that the HCQ/CQ could influence the MAPK cascade. The main aim of this review is to address molecular mechanisms, beyond drugs, that can be helpful against viral infection for this and future pandemics. We will highlight (1) the contribution of the MAPK cascade in viral infection and (2) the possible use of MAPK inhibitors in curbing viral infections, alone or in combination with HCQ and quinoline analogues. We are convinced that understanding the molecular patterns of viral infections will be critical for new therapeutical approaches to control this and other severe diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780227PMC
http://dx.doi.org/10.1155/2020/8827752DOI Listing

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