Evidence map›Paper›PMID 34167456›Full record

ReviewCellular & molecular biology letters2021

Autophagy receptors as viral targets.

Päivi Ylä-Anttila

Abstract readReview
In one paragraph

Review in Cellular & molecular biology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. COVID-19 therapies: do we see substantial progress?Cellular & molecular biology letters · 2022
    Article
  12. Review
  13. Tight association of autophagy and cell cycle in leukemia cells.Cellular & molecular biology letters · 2022
    Article
  14. Review
  15. Review
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

1 author.

Päivi Ylä-AnttilaDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden. paivi.ylaanttila@gmail.com.ORCID http://orcid.org/0000-0002-5794-5094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of autophagy is part of the innate immune response during viral infections. Autophagy involves the sequestration of endogenous or foreign components from the cytosol within double-membraned vesicles and the delivery of their content to the lysosomes for degradation. As part of innate immune responses, this autophagic elimination of foreign components is selective and requires specialized cargo receptors that function as links between a tagged foreign component and the autophagic machinery. Pathogens have evolved ways to evade their autophagic degradation to promote their replication, and recent research has shown autophagic receptors to be an important and perhaps previously overlooked target of viral autophagy inhibition. This is a brief summary of the recent progress in knowledge of virus-host interaction in the context of autophagy receptors.

Indexed as

AutophagyImmunity, InnateAnimalsHost-Pathogen InteractionsHumansProteasome Endopeptidase ComplexProteolysisSequestosome-1 ProteinVirus DiseasesVirusesVirus ReplicationProteasome Endopeptidase ComplexSequestosome-1 ProteinAutophagyCargoInfectionReceptorVirusesXenophagy

Identifiers

PMID34167456
PMCPMC8222950

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.