Evidence map›Paper›PMID 30031267›Full record

ArticleRedox biology2018

Dysregulation of DAF-16/FOXO3A-mediated stress responses accelerates oxidative DNA damage induced aging.

Aditi U Gurkar, Andria R Robinson, Yuxiang Cui, Xuesen Li, Shailaja K Allani, Amanda Webster, Mariya Muravia, Mohammad Fallahi, Herbert Weissbach, Paul D Robbins and 5 more

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Neuronal IL-17 controlsProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Antioxidants (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Zoledronate Extends Health Span and Survival via the Mevalonate Pathway in a FOXO-dependent Manner.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Combinatorial Approach UsingMolecules and cells · 2021
    Review
  12. Article
  13. Aging · 2020
    Observational
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
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

15 authors at 5 institutions in 1 country.

Aditi U GurkarDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Andria R RobinsonDepartment of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, United States.
Yuxiang CuiEnvironmental Toxicology Graduate Program and Department of Chemistry, University of California, Riverside, Riverside, CA, United States.
Xuesen LiDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Shailaja K AllaniCenter for Molecular Biology and Biotechnology, Florida Atlantic University, Jupiter, FL, United States.
Amanda WebsterDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Mariya MuraviaDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Mohammad FallahiDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Herbert WeissbachCenter for Molecular Biology and Biotechnology, Florida Atlantic University, Jupiter, FL, United States.
Paul D RobbinsDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States.
Yinsheng WangEnvironmental Toxicology Graduate Program and Department of Chemistry, University of California, Riverside, Riverside, CA, United States.
Eric E KelleyDepartment of Physiology and Pharmacology, West Virginia University, Morgantown, WV, United States.
Claudette M St CroixDepartment of Cell Biology, Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, PA, United States.
Laura J NiedernhoferDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States. Electronic address: lniedern@umn.edu.
Matthew S GillDepartment of Molecular Medicine, Center on Aging, The Scripps Research Institute, Jupiter, FL, United States. Electronic address: mgill@scripps.edu.
Scripps Research Institute · USFlorida Atlantic University · USUniversity of California, Riverside · USUniversity of Pittsburgh · USWest Virginia University · US

Funding

VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Caterina Rosano · 2004 to 2026
$28.6M
Validation and characterization of the identified variants associated with human longevity in mouse modelsU19AG056278 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI JAN VIJG · 2017 to 2026
$24.5M
PROTEOMICSP01AG043376 · NIA · UNIVERSITY OF MINNESOTA · PI ROBBINS, PAUL D. · 2013 to 2019
$11.2M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
The contribution of DNA interstrand crosslinks to agingR01ES016114 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIEDERNHOFER, LAURA JANE · 2007 to 2011
$2.5M
Modulators of DNA damage associated nucleo-mitochondrial communication in agingR00AG049126 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GURKAR, ADITI U · 2017 to 2019
$835k
The role of spin genes in autophagy and lifespan in C. elegansR21AG049447 · NIA · SCRIPPS FLORIDA · PI GILL, MATTHEW SIMON · 2017 to 2018
$532k
Genetic and Molecular Analysis of a Novel Insulin Regulatory ProteinR21AG050172 · NIA · SCRIPPS FLORIDA · PI GILL, MATTHEW SIMON · 2017 to 2018
$524k
Modulators of DNA damage associated nucleo-mitochondrial communication in agingK99AG049126 · NIA · SCRIPPS FLORIDA · PI GURKAR, ADITI U · 2015 to 2016
$203k
NIA NIH HHS K99 AG049126NIA NIH HHS P01 AG043376NIA NIH HHS P30 AG024827NIA NIH HHS R00 AG049126NIA NIH HHS R21 AG049447NIA NIH HHS R21 AG050172NIA NIH HHS U19 AG056278NIEHS NIH HHS R01 ES016114NIH HHS P40 OD010440
6 · The paper itself

Abstract

DNA damage is presumed to be one type of stochastic macromolecular damage that contributes to aging, yet little is known about the precise mechanism by which DNA damage drives aging. Here, we attempt to address this gap in knowledge using DNA repair-deficient C. elegans and mice. ERCC1-XPF is a nuclear endonuclease required for genomic stability and loss of ERCC1 in humans and mice accelerates the incidence of age-related pathologies. Like mice, ercc-1 worms are UV sensitive, shorter lived, display premature functional decline and they accumulate spontaneous oxidative DNA lesions (cyclopurines) more rapidly than wild-type worms. We found that ercc-1 worms displayed early activation of DAF-16 relative to wild-type worms, which conferred resistance to multiple stressors and was important for maximal longevity of the mutant worms. However, DAF-16 activity was not maintained over the lifespan of ercc-1 animals and this decline in DAF-16 activation corresponded with a loss of stress resistance, a rise in oxidant levels and increased morbidity, all of which were cep-1/ p53 dependent. A similar early activation of FOXO3A (the mammalian homolog of DAF-16), with increased resistance to oxidative stress, followed by a decline in FOXO3A activity and an increase in oxidant abundance was observed in Ercc1

Indexed as

DNA DamageLongevityOxidative StressAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCells, CulturedDNA-Binding ProteinsEndonucleasesForkhead Transcription FactorsGene DeletionMiceMice, Inbred C57BLReactive Oxygen SpeciesCaenorhabditis elegans Proteinsdaf-16 protein, C elegansDNA-Binding ProteinsEndonucleasesErcc1 protein, mouseForkhead Transcription FactorsFOXO3a protein, C elegansReactive Oxygen SpeciesAgingDAF-16/FOXO3ADNA damageOxidative stressReactive oxygen speciesStress resistance

Identifiers

PMID30031267
PMCPMC6076207
OpenAlexW2809122250

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.