Evidence map›Paper›PMID 30261196›Full record

ArticleGene2019

Angiopoietin-like 8 (ANGPTL8) expression is regulated by miR-143-3p in human hepatocytes.

Johanna K DiStefano

Abstract read
In one paragraph

Article in Gene, 2019. 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
3.2field-weighted citation impact, top 7% 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, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Therapeutic Value of miRNAs in Coronary Artery Disease.Oxidative medicine and cellular longevity · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Loss of GlycineInternational journal of molecular sciences · 2019
    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

1 author at 1 institution in 1 country.

Johanna K DiStefanoDiabetes and Fibrotic Disease Unit, Translational Genomics Research Institute, 445 N 5th Street, Phoenix, AZ 85004, United States of America. Electronic address: jdistefano@tgen.org.
Translational Genomics Research Institute · US

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
Atlanta Clinical and Translational Science Institute (ACTSI) RenewalUL1TR000454 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$25.8M
Genetic determinants of total cholesterol levels in American IndiansR01HL093042 · NHLBI · TRANSLATIONAL GENOMICS RESEARCH INST · PI DISTEFANO, JOHANNA K · 2010 to 2014
$2.4M
Genetic determinants of lipid traits in type 2 diabetes mellitusR01HL084439 · NHLBI · TRANSLATIONAL GENOMICS RESEARCH INST · PI DISTEFANO, JOHANNA K · 2006 to 2010
$2.3M
NCATS NIH HHS UL1 TR000454NCATS NIH HHS UL1 TR002378NHLBI NIH HHS R01 HL084439NHLBI NIH HHS R01 HL093042
6 · The paper itself

Abstract

Angiopoietin-like protein 8 (ANGPTL8) is associated with reduced HDL-cholesterol levels and may contribute to the development of dyslipidemia. Factors regulating ANGPTL8 expression remain poorly understood. Here we analyzed the relationship between miRNA-143-3p and ANGPTL8 in liver cells. Using target prediction algorithms, we identified a putative binding site for miR-143-3p in the ANGPTL8 3' untranslated region (3'UTR). Exogenous miR-143-3p interacted with the ANGPTL8 3'UTR to downregulate its expression compared to scrambled sequence control. Transfection of HepG2 cells with miR-143-3p mimic or siRNA resulted in decreased or increased ANGPTL8 transcript and protein levels, respectively. Treatment of HepG2 cells with 30 mM glucose, 100 nM insulin, or 75 ng/ml lipopolysaccharide to mimic hyperglycemic, hyperinsulinemic, and proinflammatory conditions corresponded with increased miR-143-3p and ANGPTL8 levels. Inhibition of miR-143-3p amplified ANGPTL8 response to these treatments, suggesting that the miRNA acts to suppress ANGPTL8 expression under metabolically distorted conditions. These results, combined with growing evidence supporting a role for ANGPTL8 in the regulation of HDL-C metabolism, provide a better understanding of the molecular mechanisms underlying ANGPTL8 expression.

Indexed as

Angiopoietin-Like Protein 8Angiopoietin-like ProteinsBinding SitesCells, CulturedGene Expression RegulationGlucoseHepatocytesHep G2 CellsHumansInsulinLipopolysaccharidesMicroRNAsPeptide HormonesAngiopoietin-Like Protein 8Angiopoietin-like ProteinsANGPTL8 protein, humanGlucoseInsulinLipopolysaccharidesMicroRNAsMIRN143 microRNA, humanPeptide HormonesAngiopoietin-like protein 8AtherosclerosisBetatrophinHDL-CHyperglycemiaInflammationmicroRNAmiRNA, miR-143-3p

Identifiers

PMID30261196
PMCPMC6330893
OpenAlexW2893919811

What OpenQuestion holds

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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.