Evidence map›Paper›PMID 36001751›Full record

ArticleDiabetes2022

miR-130b/301b Is a Negative Regulator of Beige Adipogenesis and Energy Metabolism In Vitro and In Vivo.

Wenyi Luo, Youngsil Kim, Mary Ellen Jensen, Oana Herlea-Pana, Weidong Wang, Michael C Rudolph, Jacob E Friedman, Steven D Chernausek, Shaoning Jiang

Open access · greenAbstract read
In one paragraph

Article in Diabetes, 2022. 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
1.8field-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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  8. Pulling the trigger: Noncoding RNAs in white adipose tissue browning.Reviews in endocrine & metabolic disorders · 2024
    Review
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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

9 authors at 1 institution in 1 country.

Wenyi LuoHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Youngsil KimHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Mary Ellen JensenHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Oana Herlea-PanaDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Weidong WangHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.ORCID 0000-0003-3619-0953
Michael C RudolphHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Jacob E FriedmanHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.ORCID 0000-0002-9283-9254
Steven D ChernausekHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.ORCID 0000-0002-9927-4460
Shaoning JiangHarold Hamm Diabetes Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK.ORCID 0000-0001-6445-9900
University of Oklahoma Health Sciences Center · US

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Michael S. Businelle · 2018 to 2026
$27.1M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI HANNAFON, BETHANY · 2012 to 2022
$21.3M
Pilot Project ProgramP30GM122744 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI SUN, ZHONGJIE · 2017 to 2021
$5.5M
NCI NIH HHS P30 CA225520NIGMS NIH HHS P20 GM103639NIGMS NIH HHS P30 GM122744
6 · The paper itself

Abstract

Thermogenic brown or beige adipocytes dissipate energy in the form of heat and thereby counteract obesity and related metabolic complications. The miRNA cluster miR-130b/301b is highly expressed in adipose tissues and has been implicated in metabolic diseases as a posttranscriptional regulator of mitochondrial biogenesis and lipid metabolism. We investigated the roles of miR-130b/301b in regulating beige adipogenesis in vivo and in vitro. miR-130b/301b declined in adipose progenitor cells during beige adipogenesis, while forced overexpression of miR-130b-3p or miR-301b-3p suppressed uncoupling protein 1 (UCP1) and mitochondrial respiration, suggesting that a decline in miR-130b-3p or miR-301b-3p is required for adipocyte precursors to develop the beige phenotype. Mechanistically, miR-130b/301b directly targeted AMP-activated protein kinase (AMPKα1) and suppressed peroxisome proliferator-activated receptor γ coactivator-1α (Pgc-1α), key regulators of brown adipogenesis and mitochondrial biogenesis. Mice lacking the miR-130b/301b miRNA cluster showed reduced visceral adiposity and less weight gain. miR-130b/301b null mice exhibited improved glucose tolerance, increased UCP1 and AMPK activation in subcutaneous fat (inguinal white adipose tissue [iWAT]), and increased response to cold-induced energy expenditure. Together, these data identify the miR-130b/301b cluster as a new regulator that suppresses beige adipogenesis involving PGC-1α and AMPK signaling in iWAT and is therefore a potential therapeutic target against obesity and related metabolic disorders.

Indexed as

Adipocytes, BeigeMicroRNAsAdipogenesisAdipose Tissue, WhiteAMP-Activated Protein KinasesAnimalsEnergy MetabolismGlucoseMiceObesityPPAR gammaThermogenesisUncoupling Protein 1AMP-Activated Protein KinasesGlucoseMicroRNAsMIRN130 microRNA, mouseMIRN301 microRNA, mousePPAR gammaUncoupling Protein 1

Identifiers

PMID36001751
PMCPMC9630090
OpenAlexW4293105675

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.