Evidence map›Paper›PMID 24722248›Full record

ArticleDiabetes2014

MicroRNA-29 fine-tunes the expression of key FOXA2-activated lipid metabolism genes and is dysregulated in animal models of insulin resistance and diabetes.

C Lisa Kurtz, Bailey C E Peck, Emily E Fannin, Carine Beysen, Ji Miao, Stuart R Landstreet, Shengli Ding, Vandana Turaga, P Kay Lund, Scott Turner and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

71 citing papers in PubMed, 117 citations in OpenAlex.

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  15. Key events in cancer: Dysregulation of SREBPs.Frontiers in pharmacology · 2023
    Review
  16. Cardiac Metabolism and MiRNA Interference.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Article

11 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 1 country.

C Lisa KurtzDepartment of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Bailey C E PeckDepartment of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC Genetics and Molecular Biology Curriculum, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Emily E FanninDepartment of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Carine BeysenKineMed, Inc., Emeryville, CA.
Ji MiaoDepartment of Pediatrics, Boston Children's Hospital, Boston, MA.
Stuart R LandstreetDepartment of Medicine, School of Medicine, Vanderbilt University, Nashville, TN.
Shengli DingDepartment of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Vandana TuragaDepartment of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
P Kay LundDepartment of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Scott TurnerKineMed, Inc., Emeryville, CA.
Sudha B BiddingerDepartment of Pediatrics, Boston Children's Hospital, Boston, MA.
Kasey C VickersDepartment of Medicine, School of Medicine, Vanderbilt University, Nashville, TN.
Praveen SethupathyDepartment of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC Genetics and Molecular Biology Curriculum, University of North Carolina at Chapel Hill, Chapel Hill, NC praveen_sethupathy@med.unc.edu.
University of North Carolina at Chapel Hill · USBoston Children's Hospital · USKineMed (United States) · USVanderbilt University · US

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
UNC Initiative for Maximizing Student DevelopmentR25GM055336 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI COOK, JEANETTE GOWEN, KASH, THOMAS L. · 1996 to 2023
$12.1M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
Control of lipid metabolism in insulin resistant statesR01DK094162 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI BIDDINGER, SUDHA B · 2012 to 2015
$1.5M
Insulin Regulation of Liver X Receptor in Normal and Insulin Resistant StatesR00DK100539 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI MIAO, JI · 2016 to 2018
$747k
Circulating microRNAs Control Cholesterol Homeostasis through hepatic mechanismsK22HL113039 · NHLBI · VANDERBILT UNIVERSITY · PI VICKERS, KASEY C · 2013 to 2015
$746k
Discovery of microRNA regulatory modules controlling human pancreatic islet functR00DK091318 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SETHUPATHY, PRAVEEN · 2012 to 2014
$737k
Insulin Regulation of Liver X Receptor in Normal and Insulin Resistant StatesK99DK100539 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI MIAO, JI · 2013 to 2014
$180k
NHLBI NIH HHS K22 HL113039NHLBI NIH HHS K22-HL-113039NIDDK NIH HHS DK-091318-02NIDDK NIH HHS DK-100539NIDDK NIH HHS K99 DK091318NIDDK NIH HHS K99 DK100539NIDDK NIH HHS L40 DK065607NIDDK NIH HHS P30 DK056350NIDDK NIH HHS P30-DK-056350NIDDK NIH HHS R00 DK091318NIDDK NIH HHS R00 DK100539NIDDK NIH HHS R01 DK094162NIGMS NIH HHS GM-007092-39NIGMS NIH HHS R25 GM055336NIGMS NIH HHS R25-GM-055336-13NIGMS NIH HHS T32 GM007092PHS HHS RHL-109650
6 · The paper itself

Abstract

MicroRNAs (miRNAs) have emerged as biomarkers of metabolic status, etiological factors in complex disease, and promising drug targets. Recent reports suggest that miRNAs are critical regulators of pathways underlying the pathophysiology of type 2 diabetes. In this study, we demonstrate by deep sequencing and real-time quantitative PCR that hepatic levels of Foxa2 mRNA and miR-29 are elevated in a mouse model of diet-induced insulin resistance. We also show that Foxa2 and miR-29 are significantly upregulated in the livers of Zucker diabetic fatty (fa/fa) rats and that the levels of both returned to normal upon treatment with the insulin-sensitizing agent pioglitazone. We present evidence that miR-29 expression in human hepatoma cells is controlled in part by FOXA2, which is known to play a critical role in hepatic energy homeostasis. Moreover, we demonstrate that miR-29 fine-tunes FOXA2-mediated activation of key lipid metabolism genes, including PPARGC1A, HMGCS2, and ABHD5. These results suggest that miR-29 is an important regulatory factor in normal metabolism and may represent a novel therapeutic target in type 2 diabetes and related metabolic syndromes.

Indexed as

AnimalsCell Line, TumorDiabetes Mellitus, Type 2FemaleHepatocyte Nuclear Factor 3-betaHumansInsulin ResistanceMiceMicroRNAsModels, AnimalPioglitazoneRatsRats, ZuckerThiazolidinedionesUp-RegulationFoxa2 protein, ratHepatocyte Nuclear Factor 3-betaMicroRNAsMIRN29a microRNA, humanMIRN29 microRNA, mouseMIRN29 microRNA, ratPioglitazoneThiazolidinediones

Identifiers

PMID24722248
PMCPMC4141370
OpenAlexW2081742737

What OpenQuestion 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 OpenQuestion graph.