Evidence map›Paper›PMID 28467860›Full record

ReviewCanadian journal of physiology and pharmacology2017

Mitochondrial miRNAs in diabetes: just the tip of the iceberg.

Rohini Baradan, John M Hollander, Samarjit Das

Open access · greenAbstract readReview
In one paragraph

Review in Canadian journal of physiology and pharmacology, 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 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Challenging Cellular Homeostasis: Spatial and Temporal Regulation of miRNAs.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. MicroRNAs, Parkinson's Disease, and Diabetes Mellitus.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Mitochondrial Mechanisms in Diabetic Cardiomyopathy.Diabetes & metabolism journal · 2020
    Review
  16. Review
  17. Regulating microRNA expression: at the heart of diabetes mellitus and the mitochondrion.American journal of physiology. Heart and circulatory physiology · 2018
    Review
  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

3 authors at 2 institutions in 1 country.

Rohini Baradana Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, USA.
John M Hollanderc Division of Exercise Physiology, West Virginia University School of Medicine, Morgantown, WV 26506, USA.
Samarjit Dasa Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, USA.
Johns Hopkins University · USWest Virginia University · US

Funding

miRNA Regulation of the Mitochondrial GenomeR01HL128485 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HOLLANDER, JOHN M · 2017 to 2019
$1.3M
miRNA Regulation of the Mitochondrial GenomeR56HL128485 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HOLLANDER, JOHN M · 2015 to 2015
$410k
NHLBI NIH HHS R01 HL128485NHLBI NIH HHS R56 HL128485
6 · The paper itself

Abstract

Over the last 2 decades, mi(cro)RNAs have emerged as one of the key regulators of metabolic homeostasis. Most of the studies have highlighted that, in the cytoplasm, miRNAs directly bind to the 3'-UTR (untranslated region) of a mRNA. Conventional RNA-induced silencing complex (RISC) formation results in the post-transcriptional inhibition. This process is known to contribute to the development of metabolic diseases, including diabetes mellitus. Recent advancements with small RNA detection technologies have enabled us to identify miRNAs in the mitochondrial compartment of the cells. We have termed these miRNAs, which translocate into the mitochondria as mitochondrial miRNA, MitomiR. It has been demonstrated that MitomiRs can regulate gene expression, with some evidence even suggesting that, after translocation, MitomiRs can bind to the 3'-end of a mitochondrial gene, altering its regulation. Our main focus in this review is to highlight the potential role of MitomiR in the pathogenesis of metabolic disorders such as diabetes mellitus.

Indexed as

3' Untranslated RegionsAnimalsBinding SitesDiabetes MellitusDiabetic CardiomyopathiesEnergy MetabolismGene Expression RegulationHumansMicroRNAsMitochondriaRNARNA, Mitochondrial3' Untranslated RegionsMicroRNAsRNARNA, MitochondrialdiabètediabetesmetabolismmétabolismemicroARN mitochondrialmitochondriamitochondrial microRNAmitochondriemitomiRMitomiR

Identifiers

PMID28467860
PMCPMC5854153
OpenAlexW2610616673

What OpenQuestion holds

Textmetadata
LicenceTDM
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.