Evidence map›Paper›PMID 34880414›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2022

MiR-200c-3p targets SESN1 and represses the IL-6/AKT loop to prevent cholangiocyte activation and cholestatic liver fibrosis.

Yongfeng Song, Melanie Tran, Li Wang, Dong-Ju Shin, Jianguo Wu

Open access · hybridAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Insights on drug and gene delivery systems in liver fibrosis.Asian journal of pharmaceutical sciences · 2023
    Review
  10. Review
  11. Article
  12. 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

5 authors at 3 institutions in 2 countries.

Yongfeng SongDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.
Melanie TranDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.
Li WangIndependent Researcher, Tucson, AZ, USA.
Dong-Ju ShinDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.
Jianguo WuDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA. wuj6@ccf.org.ORCID 0000-0001-9801-5267
University of Connecticut · USCleveland Clinic Lerner College of Medicine · USFilm Independent · US

Funding

Project Two - Exercise Training Decreases Alcohol Drinking by an FGF21-Dependent MechanismP50AA024333 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI Srinivasan Dasarathy · 2016 to 2026
$19.6M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Fabio Cominelli · 2015 to 2026
$15.6M
Transcriptional and non-transcriptional functions of IRF3 in ALDR01AA027456 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAURA E. NAGY · 2019 to 2026
$3.5M
Novel Genetic Risk Factors for Alzheimer's Disease (AD) & Frontotemporal DementiaR01AG026938 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GESCHWIND, DANIEL H · 2005 to 2009
$2.5M
The microRNA Control of Alcoholic Liver Injury and Hepatic Lipid MetabolismR01AA026322 · NIAAA · UNIVERSITY OF CONNECTICUT STORRS · PI SHIN, DONG JU · 2017 to 2021
$1.8M
Microbial metabolites and Innate Immunity in AH: Biomarkers of injury and repairU01AA026938 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2018 to 2023
$1.4M
The role of PDK4 in alcohol-associated liver diseaseK01AA029474 · NIAAA · NORTHEAST OHIO MEDICAL UNIVERSITY · PI WU, JIANGUO · 2021 to 2025
$932k
Motor Unit Discharge and Slowed Motor Output in ElderlyR03AG026322 · NIA · UNIVERSITY OF DELAWARE · PI KNIGHT, CHRISTOPHER A · 2007 to 2008
$136k
NIAAA NIH HHS K01 AA029474NIAAA NIH HHS P50 AA024333NIAAA NIH HHS R01 AA026322NIAAA NIH HHS R01 AA027456NIAAA NIH HHS U01 AA026938NIDDK NIH HHS P30 DK097948
6 · The paper itself

Abstract

Cholestasis causes ductular reaction in the liver where the reactive cholangiocytes not only proliferate but also gain a neuroendocrine-like phenotype, leading to inflammatory cell infiltration and extracellular matrix deposition and contributing to the development and progression of cholestatic liver fibrosis. This study aims to elucidate the role of miR-200c in cholestasis-induced biliary liver fibrosis and cholangiocyte activation. We found that miR-200c was extremely abundant in cholangiocytes but was reduced by cholestasis in a bile duct ligation (BDL) mouse model; miR-200c was also decreased by bile acids in vitro. Phenotypically, loss of miR-200c exacerbated cholestatic liver injury, including periductular fibrosis, intrahepatic inflammation, and biliary hyperplasia in both the BDL model and the 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC) model. We identified sestrin 1 (SESN1) as a target of miR-200c. Sesn1

Indexed as

CholestasisLiver CirrhosisMicroRNAsSestrinsAnimalsBile DuctsCell Cycle ProteinsInterleukin-6LiverMiceProto-Oncogene Proteins c-aktCell Cycle ProteinsInterleukin-6MicroRNAsMirn200 microRNA, mouseProto-Oncogene Proteins c-aktSesn1 protein, mouseSestrins

Identifiers

PMID34880414
PMCPMC9042705
OpenAlexW4200207176

What OpenQuestion holds

Textmetadata
LicenceTDM
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.