Evidence map›Paper›PMID 31428222›Full record

ArticleOxidative medicine and cellular longevity2019

Protocatechuic Acid-Mediated miR-219a-5p Activation Inhibits the p66shc Oxidant Pathway to Alleviate Alcoholic Liver Injury.

Rong Fu, Junjun Zhou, Ruiwen Wang, Ruimin Sun, Dongcheng Feng, Zhecheng Wang, Yan Zhao, Li Lv, Xiaofeng Tian, Jihong Yao

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  9. Mitochondrial heterogeneity in diseases.Signal transduction and targeted therapy · 2023
    Review
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  12. Article
  13. Article
  14. Article
  15. Review
  16. Antioxidant Effects of Protocatechuic Acid and Protocatechuic Aldehyde: Old Wine in a New Bottle.Evidence-based complementary and alternative medicine : eCAM · 2021
    Review
  17. Article
  18. Article
  19. 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

10 authors at 1 institution in 1 country.

Rong FuDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Junjun ZhouDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Ruiwen WangDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Ruimin SunDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Dongcheng FengDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116044, China.
Zhecheng WangDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Yan ZhaoDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Li LvDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.ORCID https://orcid.org/0000-0003-1157-853X
Xiaofeng TianDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116044, China.
Jihong YaoDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.ORCID https://orcid.org/0000-0002-4221-6630
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alcohol abuse has become common worldwide and has been recognized as a major cause of chronic alcoholic liver disease (ALD). ALD encompasses a complex process that includes a broad scope of hepatic lesions, ranging from steatosis to cirrhosis. In particular, reactive oxygen species (ROS) are mainly involved. Numerous studies have shown that p66shc plays a significant role in ALD. Protocatechuic acid (PCA), a dihydroxybenzoic acid that is naturally found in green tea, vegetables, and fruits, has efficient free radical scavenging effects. In this study, we aimed to assess the protective effect of PCA on ALD and to evaluate the microRNA- (miRNA-) p66shc-mediated reduction of ROS formation in ALD. Our results demonstrated that PCA treatment significantly decreased p66shc expression and downstream ROS formation in ALD. miR-219a-5p, which was identified by bioinformatics and experimental analysis, was enhanced by PCA and subsequently suppressed p66shc expression. Importantly, p66shc played an essential role in the protection of PCA-stimulated miR-219a-5p overexpression. Overall, these findings show that PCA-stimulated miR-219a-5p expression mitigates ALD by reducing p66shc-mediated ROS formation. This study may contribute to the development of therapeutic interventions for ALD.

Indexed as

3' Untranslated RegionsAnimalsCell SurvivalDown-RegulationEthanolGlutathioneHepatocytesHydroxybenzoatesLiverLiver Diseases, AlcoholicMaleMiceMicroRNAsProtective AgentsRatsRats, Sprague-Dawley3' Untranslated RegionsEthanolGlutathioneHydroxybenzoatesMicroRNAsProtective Agentsprotocatechuic acidReactive Oxygen SpeciesShc1 protein, ratSrc Homology 2 Domain-Containing, Transforming Protein 1Superoxide Dismutase

Identifiers

PMID31428222
PMCPMC6683775
OpenAlexW2962902169

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.