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Targeting Multiple Signal Transduction Pathways of SARS-CoV-2: Approaches to COVID-19 Therapeutic Candidates

Authors :
Mohammad Hosein Farzaei
Esra Küpeli Akkol
Javier Echeverría
Sana Piri
Eduardo Sobarzo-Sánchez
Seyed Zachariah Moradi
Sajad Fakhri
Zeinab Nouri
Universidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
Source :
Molecules, Molecules, Vol 26, Iss 2917, p 2917 (2021), Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela, Universidad de Santiago de Compostela (USC), Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela, instname
Publication Year :
2021
Publisher :
MDPI, 2021.

Abstract

Due to the complicated pathogenic pathways of coronavirus disease 2019 (COVID-19), related medicinal therapies have remained a clinical challenge. COVID-19 highlights the urgent need to develop mechanistic pathogenic pathways and effective agents for preventing/treating future epidemics. As a result, the destructive pathways of COVID-19 are in the line with clinical symptoms induced by severe acute coronary syndrome (SARS), including lung failure and pneumonia. Accordingly, revealing the exact signaling pathways, including inflammation, oxidative stress, apoptosis, and autophagy, as well as relative representative mediators such as tumor necrosis factor-α (TNF-α), nuclear factor erythroid 2-related factor 2 (Nrf2), Bax/caspases, and Beclin/LC3, respectively, will pave the road for combating COVID-19. Prevailing host factors and multiple steps of SARS-CoV-2 attachment/entry, replication, and assembly/release would be hopeful strategies against COVID-19. This is a comprehensive review of the destructive signaling pathways and host–pathogen interaction of SARS-CoV-2, as well as related therapeutic targets and treatment strategies, including potential natural products-based candidates J.E. gratefully acknowledges funding from CONICYT (PAI/ACADEMIA N°79160109) SI

Details

Language :
English
ISSN :
14203049
Volume :
26
Issue :
10
Database :
OpenAIRE
Journal :
Molecules
Accession number :
edsair.doi.dedup.....289bd2f65c0ac9eaeabc1bde22aa8e6a