Evidence map›Paper›PMID 27461402›Full record

ArticleNature communications2016

Lkb1 controls brown adipose tissue growth and thermogenesis by regulating the intracellular localization of CRTC3.

Tizhong Shan, Yan Xiong, Pengpeng Zhang, Zhiguo Li, Qingyang Jiang, Pengpeng Bi, Feng Yue, Gongshe Yang, Yizhen Wang, Xiaoqi Liu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 120 citations in OpenAlex.

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  12. miR-424(322)-5p targetsActa biochimica et biophysica Sinica · 2023
    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

11 authors at 3 institutions in 2 countries.

Tizhong ShanDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Yan XiongDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Pengpeng ZhangDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Zhiguo LiDepartment of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Qingyang JiangDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Pengpeng BiDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Feng YueDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Gongshe YangLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.
Yizhen WangCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Xiaoqi LiuDepartment of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Shihuan KuangDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.ORCID 0000-0001-9180-3180
Purdue University West Lafayette · USNorthwest A&F University · CNZhejiang University · CN

Funding

Treatment of Castration-resistant Prostate Cancer (CRPC)R01CA196835 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2016 to 2020
$1.7M
Notch Regulation of Stem Cell Fate in MuscleR01AR060652 · NIAMS · PURDUE UNIVERSITY · PI KUANG, SHIHUAN · 2010 to 2014
$1.6M
NIAMS NIH HHS R01 AR060652
6 · The paper itself

Abstract

Brown adipose tissue (BAT) dissipates energy through Ucp1-mediated uncoupled respiration and its activation may represent a therapeutic strategy to combat obesity. Here we show that Lkb1 controls BAT expansion and UCP1 expression in mice. We generate adipocyte-specific Lkb1 knockout mice and show that, compared with wild-type littermates, these mice exhibit elevated UCP1 expression in BAT and subcutaneous white adipose tissue, have increased BAT mass and higher energy expenditure. Consequently, KO mice have improved glucose tolerance and insulin sensitivity, and are more resistant to high-fat diet (HFD)-induced obesity. Deletion of Lkb1 results in a cytoplasm to nuclear translocation of CRTC3 in brown adipocytes, where it recruits C/EBPβ to enhance Ucp1 transcription. In parallel, the absence of Lkb1 also suppresses AMPK activity, leading to activation of the mTOR signalling pathway and subsequent BAT expansion. These data suggest that inhibition of Lkb1 or its downstream signalling in adipocytes could be a novel strategy to increase energy expenditure in the context of obesity, diabetes and other metabolic diseases.

Indexed as

ThermogenesisAdenylate KinaseAdipocytesAdiponectinAdipose Tissue, BrownAdipose Tissue, WhiteAMP-Activated Protein KinasesAnimalsCCAAT-Enhancer-Binding Protein-betaCell NucleusDiet, High-FatGene DeletionGene Expression ProfilingGlucoseGlucose Tolerance TestHEK293 CellsAdenylate KinaseAdiponectinAMP-Activated Protein KinasesCCAAT-Enhancer-Binding Protein-betaCebpb protein, mouseCre recombinaseCRTC3 protein, mouseGlucoseIntegrasesProtein Serine-Threonine KinasesStk11 protein, mouseTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID27461402
PMCPMC4974456
OpenAlexW2487910216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.