Evidence map›Paper›PMID 27611085›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Novel protective mechanism of reducing renal cell damage in diabetes: Activation AMPK by AICAR increased NRF2/OGG1 proteins and reduced oxidative DNA damage.

Samy L Habib, Anamika Yadav, Dawit Kidane, Robert H Weiss, Sitai Liang

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

  1. Review
  2. NRF2 Dysregulation and Therapeutic Insights Across Chronic Kidney Diseases.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. Roles of NRF2 in DNA damage repair.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. OGG1 in the Kidney: Beyond Base Excision Repair.Oxidative medicine and cellular longevity · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Critical Role for AMPK in Metabolic Disease-Induced Chronic Kidney Disease.International journal of molecular sciences · 2020
    Review
  19. Review
  20. The Dephosphorylation of p70S6 (ThrNeurotoxicity research · 2020
    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

5 authors.

Samy L Habiba Department of Cellular and Structural Biology , University of Texas Health Science Center , San Antonio , TX , USA.
Anamika Yadava Department of Cellular and Structural Biology , University of Texas Health Science Center , San Antonio , TX , USA.
Dawit Kidanec Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, Dell Pediatric Research Institute , Austin , TX , USA.
Robert H Weissd Division of Nephrology and Cancer Center, University of California at Davis , Davis , CA , USA.
Sitai Lianga Department of Cellular and Structural Biology , University of Texas Health Science Center , San Antonio , TX , USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure of renal cells to high glucose (HG) during diabetes has been recently proposed to be involved in renal injury. In the present study, we investigated a potential mechanism by which AICAR treatment regulates the DNA repair enzyme, 8-oxoG-DNA glycosylase (OGG1) in renal proximal tubular mouse cells exposed to HG and in kidney of db/db mice. Cells treated with HG for 2 days show inhibition in OGG1 promoter activity as well as OGG1 and Nrf2 protein expression. In addition, activation of AMPK by AICAR resulted in an increase raptor phosphorylation at Ser

Indexed as

DNA DamageAdaptor Proteins, Signal TransducingAminoimidazole CarboxamideAMP-Activated Protein KinasesAnimalsBase SequenceCarrier ProteinsDiabetes MellitusDNA GlycosylasesDown-RegulationEnzyme ActivationGlucoseHEK293 CellsHumansKidneyKidney Tubules, ProximalAdaptor Proteins, Signal TransducingAICA ribonucleotideAminoimidazole CarboxamideAMP-Activated Protein KinasesCarrier ProteinsDNA GlycosylasesGlucoseMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesNF-E2-Related Factor 2Ogg1 protein, mouseProto-Oncogene Proteins c-aktRapamycin-Insensitive Companion of mTOR ProteinRegulatory-Associated Protein of mTORRibonucleotidesrictor protein, mouseRNA, MessengerRptor protein, mouseTOR Serine-Threonine KinasesAICARAMPKdiabetesmTORNrf2OGG1

Identifiers

PMID27611085
PMCPMC5134712

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.