Evidence map›Paper›PMID 34206057›Full record

ReviewInternational journal of molecular sciences2021

Autophagy, Unfolded Protein Response, and Neuropilin-1 Cross-Talk in SARS-CoV-2 Infection: What Can Be Learned from Other Coronaviruses.

Morvarid Siri, Sanaz Dastghaib, Mozhdeh Zamani, Nasim Rahmani-Kukia, Kiarash Roustai Geraylow, Shima Fakher, Fatemeh Keshvarzi, Parvaneh Mehrbod, Mazaher Ahmadi, Pooneh Mokarram and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Morvarid SiriAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.ORCID 0000-0002-5556-2102
Sanaz DastghaibEndocrinology and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz 7193635899, Iran.ORCID 0000-0001-8553-9221
Mozhdeh ZamaniAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.ORCID 0000-0001-7856-6029
Nasim Rahmani-KukiaDepartment of Biochemistry, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.ORCID 0000-0002-3004-6283
Kiarash Roustai GeraylowStudent Research Committee, Semnan University of Medical Sciences, Semnan 3514799422, Iran.ORCID 0000-0002-4366-6764
Shima FakherDepartment of Biochemistry, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.
Fatemeh KeshvarziDepartment of Biochemistry, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.
Parvaneh MehrbodInfluenza and Respiratory Viruses Department, Pasteur Institute of Iran, Tehran 1316943551, Iran.ORCID 0000-0002-8391-9228
Mazaher AhmadiFaculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838695, Iran.ORCID 0000-0001-9969-170X
Pooneh MokarramAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.ORCID 0000-0002-9717-0473
Kevin M CoombsDepartment of Medical Microbiology and Infectious Diseases, Rady Faculty of Health Sciences, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.
Saeid GhavamiAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz 7134845794, Iran.ORCID 0000-0001-5948-508X
Shiraz University of Medical Sciences · IRBu-Ali Sina University · IRPasteur Institute of Iran · IRSemnan University of Medical Sciences · IRUniversity of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic is caused by the 2019-nCoV/SARS-CoV-2 virus. This severe acute respiratory syndrome is currently a global health emergency and needs much effort to generate an urgent practical treatment to reduce COVID-19 complications and mortality in humans. Viral infection activates various cellular responses in infected cells, including cellular stress responses such as unfolded protein response (UPR) and autophagy, following the inhibition of mTOR. Both UPR and autophagy mechanisms are involved in cellular and tissue homeostasis, apoptosis, innate immunity modulation, and clearance of pathogens such as viral particles. However, during an evolutionary arms race, viruses gain the ability to subvert autophagy and UPR for their benefit. SARS-CoV-2 can enter host cells through binding to cell surface receptors, including angiotensin-converting enzyme 2 (ACE2) and neuropilin-1 (NRP1). ACE2 blockage increases autophagy through mTOR inhibition, leading to gastrointestinal complications during SARS-CoV-2 virus infection. NRP1 is also regulated by the mTOR pathway. An increased NRP1 can enhance the susceptibility of immune system dendritic cells (DCs) to SARS-CoV-2 and induce cytokine storm, which is related to high COVID-19 mortality. Therefore, signaling pathways such as mTOR, UPR, and autophagy may be potential therapeutic targets for COVID-19. Hence, extensive investigations are required to confirm these potentials. Since there is currently no specific treatment for COVID-19 infection, we sought to review and discuss the important roles of autophagy, UPR, and mTOR mechanisms in the regulation of cellular responses to coronavirus infection to help identify new antiviral modalities against SARS-CoV-2 virus.

Indexed as

AutophagyUnfolded Protein ResponseAntiviral AgentsCOVID-19HumansMolecular ChaperonesNeuropilin-1SARS-CoV-2Signal TransductionViral Envelope ProteinsAntiviral AgentsMolecular ChaperonesNeuropilin-1Viral Envelope ProteinsautophagyCOVID-19endoplasmic reticulum stressSARS-CoV-2unfolded protein response

Identifiers

PMID34206057
PMCPMC8199451
OpenAlexW3166413205

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.