Evidence map›Paper›PMID 35004133›Full record

ArticleAnalytical cellular pathology (Amsterdam)2021

MicroRNA-137-3p Improves Nonalcoholic Fatty Liver Disease through Activating AMPK

Yuanjie Yu, Chunping He, Shiyun Tan, Mengjun Huang, Yitian Guo, Ming Li, Qian Zhang

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2024
    Article
  5. Review
  6. Update on genetics and epigenetics in metabolic associated fatty liver disease.Therapeutic advances in endocrinology and metabolism · 2022
    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

7 authors at 2 institutions in 1 country.

Yuanjie YuDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.ORCID https://orcid.org/0000-0002-0924-0882
Chunping HeDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.
Shiyun TanDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.
Mengjun HuangDepartment of Nutrition, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430014, Hubei, China.
Yitian GuoDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.
Ming LiDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.ORCID https://orcid.org/0000-0002-8601-9890
Qian ZhangDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.ORCID https://orcid.org/0000-0003-1053-1588
Wuhan University · CNCentral Hospital of Wuhan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is one of the most common chronic liver diseases worldwide and can develop to nonalcoholic steatohepatitis and later hepatic cirrhosis with a high prevalence to hepatocellular carcinoma. Oxidative stress and chronic hepatic inflammation are implicated in the pathogenesis of NAFLD. MicroRNA-137-3p (miR-137-3p) are associated with oxidative stress and inflammation; however, its role and mechanism in NAFLD remain unclear. Mice were fed with a high-fat diet (HFD) for 24 weeks to establish the NAFLD model. To overexpress or suppress hepatic miR-137-3p expression, mice were intraperitoneally injected with the agomir, antagomir, or respective controls of miR-137-3p at a dose of 100 mg/kg weekly for 6 consecutive weeks before the mice were sacrificed. To validate the involvement of AMP-activated protein kinase alpha (AMPK

Indexed as

Gene Expression Regulation3' Untranslated RegionsAMP-Activated Protein KinasesAnimalsCells, CulturedCyclic Nucleotide Phosphodiesterases, Type 4Diet, High-FatEnzyme ActivationHEK293 CellsHumansMaleMiceMice, Inbred C57BLMicroRNAsNon-alcoholic Fatty Liver DiseasePhosphodiesterase 4 Inhibitors3' Untranslated RegionsAMP-Activated Protein KinasesCyclic Nucleotide Phosphodiesterases, Type 4MicroRNAsMIRN137 microRNA, mousePDE4D protein, mousePhosphodiesterase 4 InhibitorsRolipram

Identifiers

PMID35004133
PMCPMC8731301
OpenAlexW4200215252

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.