Evidence map›Paper›PMID 25587857›Full record

ReviewMolecular medicine (Cambridge, Mass.)2015

Sirtuin 1: A Target for Kidney Diseases.

Lili Kong, Hao Wu, Wenhua Zhou, Manyu Luo, Yi Tan, Lining Miao, Lu Cai

Open access · goldAbstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Serum α-Klotho and SIRT1 - Relationship with graft function, inflammation and hospitalization rates in kidney transplant recipients.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Observational
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. NADCells · 2022
    Review
  11. Review
  12. Article
  13. Article
  14. Claudins in kidney health and disease.Kidney research and clinical practice · 2022
    Article
  15. Article
  16. Review
  17. Sirtuin Family and Diabetic Kidney Disease.Frontiers in endocrinology · 2022
    Review
  18. TFP5-Mediated CDK5 Activity Inhibition Improves Diabetic NephropathyFrontiers in cell and developmental biology · 2022
    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

7 authors at 3 institutions in 2 countries.

Lili KongDepartment of Nephrology, the Second Hospital of Jilin University, Changchun, China.
Hao WuDepartment of Nephrology, the Second Hospital of Jilin University, Changchun, China.
Wenhua ZhouDepartment of Nephrology, the Second Hospital of Jilin University, Changchun, China.
Manyu LuoDepartment of Nephrology, the Second Hospital of Jilin University, Changchun, China.
Yi TanKosair Children's Hospital Research Institute, Department of Pediatrics, University of Louisville, Louisville, Kentucky.
Lining MiaoDepartment of Nephrology, the Second Hospital of Jilin University, Changchun, China.
Lu CaiKosair Children's Hospital Research Institute, Department of Pediatrics, University of Louisville, Louisville, Kentucky.
Second Affiliated Hospital of Jilin University · CNUniversity of Louisville · USKosair Children's Hospital · US

Funding

Metabolomics study on the preventive mechanisms for LDR on diabetic nephropathyR01DK091338 · NIDDK · UNIVERSITY OF LOUISVILLE · PI CAI, LU · 2013 to 2014
$900k
NIDDK NIH HHS 1R01DK 091338-01A1NIDDK NIH HHS R01 DK091338
6 · The paper itself

Abstract

Sirtuin 1 (SIRT1) is an evolutionarily conserved NAD(+)-dependent histone deacetylase that is necessary for caloric restriction-related lifespan extension. SIRT1, as an intracellular energy sensor, detects the concentration of intracellular NAD(+) and uses this information to adapt cellular energy output to cellular energy requirements. Previous studies on SIRT1 have confirmed its beneficial effects on cellular immunity to oxidative stress, reduction of fibrosis, suppression of inflammation, inhibition of apoptosis, regulation of metabolism, induction of autophagy and regulation of blood pressure. All of the above biological processes are involved in the pathogenesis of kidney diseases. Therefore, the activation of SIRT1 may become a therapeutic target to improve the clinical outcome of kidney diseases. In this review, we give an overview of SIRT1 and its molecular targets as well as SIRT1-modulated biological processes, with a particular focus on the role of SIRT1 in kidney diseases.

Indexed as

AnimalsGene Expression RegulationHumansKidney DiseasesProtein BindingSignal TransductionSirtuin 1Sirtuin 1

Identifiers

PMID25587857
PMCPMC4461580
OpenAlexW133756765

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.