Evidence map›Paper›PMID 32455716›Full record

ArticleInternational journal of molecular sciences2020

Exogenous Therapeutics of Microrna-29a Attenuates Development of Hepatic Fibrosis in Cholestatic Animal Model through Regulation of Phosphoinositide 3-Kinase p85 Alpha.

Ya-Ling Yang, Feng-Sheng Wang, Hung-Yu Lin, Ying-Hsien Huang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Role of noncoding RNAs in liver fibrosis.World journal of gastroenterology · 2023
    Review
  6. MiR-29a Curbs Hepatocellular Carcinoma Incidence via Targeting ofInternational journal of molecular sciences · 2022
    Article
  7. Article
  8. Review
  9. International journal of molecular sciences · 2021
    Article
  10. Review
  11. The role of autophagy in hepatic fibrosis.American journal of translational research · 2021
    Review
  12. Review
  13. 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

4 authors at 1 institution in 1 country.

Ya-Ling YangDepartment of Anesthesiology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 833, Taiwan.
Feng-Sheng WangCore Laboratory for Phenomics & Diagnostics, Department of Medical Research, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 833, Taiwan.
Hung-Yu LinDepartment of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 833, Taiwan.ORCID 0000-0002-9035-5408
Ying-Hsien HuangDepartment of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 833, Taiwan.ORCID 0000-0002-7127-0046
Chang Gung University · TW

Funding

Kaohsiung Chang Gung Memorial Hospital CMRPG8I0491, 8I0492 and 8G1342Ministry of Science and Technology, Taiwan 106-2314-B-182A-141 -MY3 and 108-2811-B-182A-509National Health Research Institutes NHRI-EX107-10736SI
6 · The paper itself

Abstract

Recent studies have found that microRNA-29a (miR-29a) levels are significantly lower in fibrotic livers, as shown with human liver cirrhosis. Such downregulation influences the activation of hepatic stellate cells (HSC). Phosphoinositide 3-kinase p85 alpha (PI3KP85α) is implicated in the regulation of proteostasis mitochondrial integrity and unfolded protein response (UPR) and apoptosis in hepatocytes. This study aimed to investigate the potential therapeutic role of miR-29a in a murine bile duct ligation (BDL)-cholestatic injury and liver fibrosis model. Mice were assigned to four groups: sham, BDL, BDL + scramble miRs, and BDL + miR-29a-mimic. Liver fibrosis and inflammation were assessed by histological staining and mRNA/protein expression of representative markers. Exogenous therapeutics of miR-29a in BDL-stressed mice significantly attenuated glutamic oxaloacetic transaminase (GOT)/glutamic-pyruvic transaminase (GPT) and liver fibrosis, and caused a significant downregulation in markers related to inflammation (IL-1β), fibrogenesis (TGF-β1, α-SMA, and COL1α1), autophagy (p62 and LC3B II), mitochondrial unfolded protein response (UPR

Indexed as

Alanine TransaminaseAnimalsAspartate AminotransferasesATP-Dependent ProteasesChaperonin 60CholestasisClass Ia Phosphatidylinositol 3-KinaseCollagen Type IHep G2 CellsHumansInterleukin-1betaLiverLiver CirrhosisMiceMice, Inbred C57BLMicroRNAsAlanine TransaminaseAspartate AminotransferasesATP-Dependent ProteasesChaperonin 60Class Ia Phosphatidylinositol 3-KinaseCollagen Type IDdit3 protein, mouseHspd1 protein, mouseInterleukin-1betaLONP1 protein, mouseMicroRNAsMIRN29 microRNA, mouseMitochondrial ProteinsPik3r1 protein, mouseTranscription Factor CHOPTransforming Growth Factor betafibrosishepatitismicroRNA-29amitochondrial unfolded protein responsePI3KP85αproteostasistherapeutics

Identifiers

PMID32455716
PMCPMC7279217
OpenAlexW3027385199

What OpenQuestion holds

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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.