Evidence map›Paper›PMID 25187367›Full record

ArticleDiabetes2015

Glucocorticoids transcriptionally regulate miR-27b expression promoting body fat accumulation via suppressing the browning of white adipose tissue.

Xiaocen Kong, Jing Yu, Jianhua Bi, Hanmei Qi, Wenjuan Di, Lin Wu, Long Wang, Juanmin Zha, Shan Lv, Feng Zhang and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Glucocorticoid-Induced Hyperglycemia: A Neglected Problem.Endocrinology and metabolism (Seoul, Korea) · 2024
    Review
  10. Dexamethasone Inhibits White Adipose Tissue Browning.International journal of molecular sciences · 2024
    Article
  11. Article
  12. Weighing in on the role of brown adipose tissue for treatment of obesity.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. The Roles of Androgens in Humans: Biology, Metabolic Regulation and Health.International journal of molecular sciences · 2022
    Review
  20. Review

5 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

16 authors at 3 institutions in 2 countries.

Xiaocen KongDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Jing YuDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Jianhua BiDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Hanmei QiDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Wenjuan DiDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Lin WuDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Long WangDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Juanmin ZhaDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Shan LvDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Feng ZhangDepartment of General Surgery, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Yan LiMetabolic Syndrome Research Center of Central South University, Institute of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, People's Republic of China.
Fang HuMetabolic Syndrome Research Center of Central South University, Institute of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, People's Republic of China.
Feng LiuMetabolic Syndrome Research Center of Central South University, Institute of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, People's Republic of China.
Hong ZhouBone Research Program, ANZAC Research Institute, University of Sydney, Sydney, Australia.
Juan LiuDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China dinggx@njmu.edu.cn lioujane@njmu.edu.cn.
Guoxian DingDepartment of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China dinggx@njmu.edu.cn lioujane@njmu.edu.cn.
Nanjing Medical University · CNSecond Xiangya Hospital of Central South University · CNUniversity of Sydney · AU

Funding

Regulation and Function of Adiponectin OligomerizationR01DK076902 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LIU, FENG · 2008 to 2017
$2.9M
NIDDK NIH HHS R01 DK076902
6 · The paper itself

Abstract

Long-term glucocorticoid (GC) treatment induces central fat accumulation and metabolic dysfunction. We demonstrate that microRNA-27b (miR-27b) plays a central role in the pathogenesis of GC-induced central fat accumulation. Overexpression of miR-27b had the same effects as dexamethasone (DEX) treatment on the inhibition of brown adipose differentiation and the energy expenditure of primary adipocytes. Conversely, antagonizing miR-27b function prevented DEX suppression of the expression of brown adipose tissue-specific genes. GCs transcriptionally regulate miR-27b expression through a GC receptor-mediated direct DNA-binding mechanism, and miR-27b suppresses browning of white adipose tissue (WAT) by targeting the three prime untranslated region of Prdm16. In vivo, antagonizing miR-27b function in DEX-treated mice resulted in the efficient induction of brown adipocytes within WAT and improved GC-induced central fat accumulation. Collectively, these results indicate that miR-27b functions as a central target of GC and as an upstream regulator of Prdm16 to control browning of WAT and, consequently, may represent a potential target in preventing obesity.

Indexed as

Adipose TissueAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsAnimals, Genetically ModifiedDexamethasoneDNA-Binding ProteinsGene Expression RegulationMiceMicroRNAsTranscription FactorsDexamethasoneDNA-Binding ProteinsMicroRNAsMirn27 microRNA, mousePrdm16 protein, mouseTranscription Factors

Identifiers

PMID25187367
PMCPMC4876791
OpenAlexW2132328706

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.