Evidence map›Paper›PMID 27966196›Full record

ReviewJournal of physiology and biochemistry2017

MicroRNAs 33, 122, and 208: a potential novel targets in the treatment of obesity, diabetes, and heart-related diseases.

Osama Abo Alrob, Said Khatib, Saleh A Naser

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Journal of physiology and biochemistry, 2017. 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
2.0field-weighted citation impact, top 15% 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, 29 citations in OpenAlex.

  1. Article
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  4. Review
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  7. Article
  8. Epigenetics, microRNA and Metabolic Syndrome: A Comprehensive Review.International journal of molecular sciences · 2021
    Review
  9. Article
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  11. Downregulation of miR-33 Has Protective Effect Against Aβ₂₅₋₃₅-Induced Injury in SH-SH-SY5Y Cells.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  12. Article
  13. Long-Chain Non-Coding RNA (lncRNA) MT1JP Suppresses Biological Activities of Lung Cancer by Regulating miRNA-423-3p/Bim Axis.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  14. Article
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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

3 authors at 3 institutions in 2 countries.

Osama Abo AlrobFaculty of Pharmacy, Yarmouk University, P.O Box 566, Irbid, 21163, Jordan. Osama.Yousef@yu.edu.jo.
Said KhatibFaculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Saleh A NaserBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, USA.
Jordan University of Science and Technology · JOUniversity of Central Florida · USYarmouk University · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite decades of research, obesity and diabetes remain major health problems in the USA and worldwide. Among the many complications associated with diabetes is an increased risk of cardiovascular diseases, including myocardial infarction and heart failure. Recently, microRNAs have emerged as important players in heart disease and energy regulation. However, little work has investigated the role of microRNAs in cardiac energy regulation. Both human and animal studies have reported a significant increase in circulating free fatty acids and triacylglycerol, increased cardiac reliance on fatty acid oxidation, and subsequent decrease in glucose oxidation which all contributes to insulin resistance and lipotoxicity seen in obesity and diabetes. Importantly, MED13 was initially identified as a negative regulator of lipid accumulation in Drosophilia. Various metabolic genes were downregulated in MED13 transgenic heart, including sterol regulatory element-binding protein. Moreover, miR-33 and miR-122 have recently revealed as key regulators of lipid metabolism. In this review, we will focus on the role of microRNAs in regulation of cardiac and total body energy metabolism. We will also discuss the pharmacological and non-pharmacological interventions that target microRNAs for the treatment of obesity and diabetes.

Indexed as

Models, BiologicalAnimalsAnti-Obesity AgentsCardiotonic AgentsDiabetes MellitusDrug DesignEnergy MetabolismGene Expression RegulationHeart DiseasesHumansHypoglycemic AgentsLipid MetabolismMicroRNAsMolecular Targeted TherapyObesityAnti-Obesity AgentsCardiotonic AgentsHypoglycemic AgentsMicroRNAsMIRN122 microRNA, humanMIRN208 microRNA, humanMIRN33a microRNA, humanDiabetesFatty acid oxidationLipid metabolismMED13MicroRNAsObesity

Identifiers

PMID27966196
OpenAlexW2567298997

What Socratic holds

Textmetadata
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 Socratic graph.