Evidence map›Paper›PMID 32323768›Full record

ArticleMolecular medicine reports2020

ATG7 promotes autophagy in sepsis‑induced acute kidney injury and is inhibited by miR‑526b.

Ying Liu, Jilai Xiao, Jiakui Sun, Wenxiu Chen, Shu Wang, Run Fu, Han Liu, Hongguang Bao

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 17 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

8 authors at 1 institution in 1 country.

Ying Liu *Department of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Jilai Xiao *Department of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Jiakui Sun *Department of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Wenxiu ChenDepartment of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Shu WangDepartment of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Run FuDepartment of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Han LiuDepartment of Critical Care Medicine, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Hongguang BaoDepartment of Anesthesiology, The Affiliated Nanjing First Hospital of Nanjing Medical University, Nanjing, Jiangsu 210006, P.R. China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is considered to be the most common contributing factor in the development of acute kidney injury (AKI). However, the mechanisms by which sepsis leads to AKI remain unclear. Autophagy is important for a number of fundamental biological activities and plays a key role in numerous different diseases. The present study demonstrated that autophagy is involved in sepsis‑induced kidney injury and upregulates ATG7, LC3 and Beclin I. In addition, it was revealed that miR‑526b is decreased in sepsis‑induced kidney injury, and miR‑526b was identified as a direct regulator of ATG7. Furthermore, the present study investigated the biological effects of ATG7 inhibited by miR‑526b and demonstrated that miR‑526b could promote cell viability by inhibiting autophagy, potentially through targeting ATG7. In conclusion, the present study highlights the role of autophagy in sepsis‑induced AKI, and miR‑526b in regulating autophagy through targeting ATG7, which suggested that miR‑526b may be a molecular therapeutic target for sepsis‑induced AKI.

Indexed as

Acute Kidney InjuryAnimalsAutophagyAutophagy-Related Protein 7Beclin-1Cell LineCell SurvivalHumansKidneyMaleMiceMice, Inbred BALB CMicroRNAsMicrotubule-Associated ProteinsRNA, Small InterferingSepsisAutophagy-Related Protein 7Beclin-1Becn1 protein, mouseMap1lc3b protein, mouseMicroRNAsMicrotubule-Associated ProteinsMIRN526 microRNA, humanRNA, Small Interferingacute kidney injuryaTG7autophagymicrorna

Identifiers

PMID32323768
PMCPMC7115197
OpenAlexW3009013444

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.