Evidence map›Paper›PMID 34977022›Full record

ReviewFrontiers in cell and developmental biology2021

Studies Progression on the Function of Autophagy in Viral Infection.

Weizheng Liang, Huimin Liu, Junli He, Lisha Ai, Qingxue Meng, Weiwen Zhang, Chengwei Yu, Hao Wang, Hui Liu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Frontiers in pharmacology · 2022
    Article
  5. Article
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

9 authors at 3 institutions in 1 country.

Weizheng LiangHarbin Institute of Technology, Harbin, China.
Huimin LiuDepartment of Infectious Diseases, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Junli HeDepartment of Pediatrics, Shenzhen University General Hospital, Shenzhen, China.
Lisha AiDepartment of Teaching and Research, Shenzhen University General Hospital, Shenzhen, China.
Qingxue MengDepartment of Science, Southern University of Science and Technology, Shenzhen, China.
Weiwen ZhangDepartment of Gynaecology and Obstetrics, Shenzhen University General Hospital, Shenzhen, China.
Chengwei YuSchool of Future Technology, University of Chinese Academy of Sciences, Beijing, China.
Hao WangDepartment of Science, Southern University of Science and Technology, Shenzhen, China.
Hui LiuDepartment of Hepatobiliary Surgery, Shenzhen University General Hospital, Shenzhen, China.
Shenzhen University · CNArmy Medical University · CNHarbin Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a conservative lysosomal catabolic pathway commonly seen in eukaryotic cells. It breaks down proteins and organelles by forming a two-layer membrane structure of autophagosomes and circulating substances and maintaining homeostasis. Autophagy can play a dual role in viral infection and serve either as a pro-viral factor or an antiviral defense element dependent on the virus replication cycle. Recent studies have suggested the complicated and multidirectional role of autophagy in the process of virus infection. On the one hand, autophagy can orchestrate immunity to curtail infection. On the other hand, some viruses have evolved strategies to evade autophagy degradation, facilitating their replication. In this review, we summarize recent progress of the interaction between autophagy and viral infection. Furthermore, we highlight the link between autophagy and SARS-CoV-2, which is expected to guide the development of effective antiviral treatments against infectious diseases.

Indexed as

autophagycoronavirusinfectionSARS-CoV-2virus

Identifiers

PMID34977022
PMCPMC8716779
OpenAlexW4200511395

What Socratic 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 Socratic graph.