Evidence map›Paper›PMID 27022940›Full record

ArticleEndocrine2016

SIRT1 prevents hyperuricemia via the PGC-1α/PPARγ-ABCG2 pathway.

Juan Wang, Xiao-Xia Zhu, Lei Liu, Yu Xue, Xue Yang, He-Jian Zou

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Novel Role of the SIRT1 in Endocrine and Metabolic Diseases.International journal of biological sciences · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Sirtuin deficiency and the adverse effects of fructose and uric acid synthesis.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Review
  12. Multidrug efflux transporter ABCG2: expression and regulation.Cellular and molecular life sciences : CMLS · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Bergenin as a Novel Urate-Lowering Therapeutic Strategy for Hyperuricemia.Frontiers in cell and developmental biology · 2020
    Article
  19. Article
  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

6 authors at 2 institutions in 1 country.

Juan WangDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Xiao-Xia ZhuDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China. zhuxiaoxia@medmail.com.cn.
Lei LiuDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Yu XueDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Xue YangDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
He-Jian ZouDivision of Rheumatology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China. hjzou@fudan.edu.cn.
Fudan University · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silent information regulator T1 (SIRT1) plays several key roles in the regulation of lipid and glucose homoeostasis. In this study, we investigated the potential role of SIRT1 in hyperuricemia and explored possible mechanisms. Significant hyperuricemia was detected in C57BL/6 mice treated with oxonate and yeast polysaccharide. Resveratrol (RSV), a specific SIRT1 activator, was administered to the mice. SIRT1 suppressed the increased serum uric acid level but up-regulated the expression of urate transporter ATP-binding cassette subfamily G member 2 (ABCG2) in the ileum of hyperuricemic mice. In a human colon carcinoma cell line, SIRT1 promoted ABCG2 production through the deacetylation of peroxisome proliferator-activated receptor (PPAR) γ co-activator 1α (PGC-1α), which then activated the effectors of PPARγ. Interestingly, the SIRT1-induced up-regulation of ABCG2 was significantly inhibited when PGC-1α or PPARγ was blocked by siRNA transfection. Our data demonstrated that SIRT1 and its activator, RSV, have clear anti-hyperuricemia functions in this mouse model. One possible mechanism is the activation of ABCG2 in the ileum through the PGC-1α/PPARγ pathway.

Indexed as

AnimalsATP Binding Cassette Transporter, Subfamily G, Member 2Cell Line, TumorHumansHyperuricemiaIleumMiceNeoplasm ProteinsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaResveratrolSignal TransductionSirtuin 1StilbenesUric AcidABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Neoplasm ProteinsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaPpargc1a protein, mouseResveratrolSirt1 protein, mouseSirtuin 1StilbenesUric AcidABCG2HyperuricemiaPGC-1αPPARγSIRT1

Identifiers

PMID27022940
OpenAlexW2312546552

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.