Evidence map›Paper›PMID 22064865›Full record

ArticleNucleic acids research2012

Interferon gamma (IFN-γ) disrupts energy expenditure and metabolic homeostasis by suppressing SIRT1 transcription.

Ping Li, Yuhao Zhao, Xiaoyan Wu, Minjie Xia, Mingming Fang, Yasumasa Iwasaki, Jiahao Sha, Qi Chen, Yong Xu, Aiguo Shen

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. SIRT1 and thrombosis.Frontiers in molecular biosciences · 2023
    Review
  11. Genetic Variants ofInternational journal of endocrinology · 2023
    Article
  12. Article
  13. Article
  14. The role of SIRT1 in the process ofFrontiers in microbiology · 2022
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article
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

10 authors at 1 institution in 1 country.

Ping LiState Key Laboratory of Reproductive Medicine and Department of Pathophysiology, Key Laboratory of Cardiovascular Disease,The Second Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Yuhao Zhao
Xiaoyan Wu
Minjie Xia
Mingming Fang
Yasumasa Iwasaki
Jiahao Sha
Qi Chen
Yong Xu
Aiguo Shen
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic inflammation impairs metabolic homeostasis and is intimately correlated with the pathogenesis of type 2 diabetes. The pro-inflammatory cytokine IFN-γ is an integral part of the metabolic inflammation circuit and contributes significantly to metabolic dysfunction. The underlying mechanism, however, remains largely unknown. In the present study, we report that IFN-γ disrupts the expression of genes key to cellular metabolism and energy expenditure by repressing the expression and activity of SIRT1 at the transcription level. Further analysis reveals that IFN-γ requires class II transactivator (CIITA) to repress SIRT1 transcription. CIITA, once induced by IFN-γ, is recruited to the SIRT1 promoter by hypermethylated in cancer 1 (HIC1) and promotes down-regulation of SIRT1 transcription via active deacetylation of core histones surrounding the SIRT1 proximal promoter. Silencing CIITA or HIC1 restores SIRT1 activity and expression of metabolic genes in skeletal muscle cells challenged with IFN-γ. Therefore, our data delineate an IFN-γ/HIC1/CIITA axis that contributes to metabolic dysfunction by suppressing SIRT1 transcription in skeletal muscle cells and as such shed new light on the development of novel therapeutic strategies against type 2 diabetes.

Indexed as

Energy MetabolismTranscription, GeneticCell LineDown-RegulationHistonesHomeostasisHumansInterferon-gammaKruppel-Like Transcription FactorsMuscle Fibers, SkeletalNuclear ProteinsPromoter Regions, GeneticSirtuin 1Trans-ActivatorsHistonesInterferon-gammaKruppel-Like Transcription FactorsMHC class II transactivator proteinNuclear ProteinsSirtuin 1Trans-Activators

Identifiers

PMID22064865
PMCPMC3287208
OpenAlexW2041098309

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.