Evidence map›Paper›PMID 30247515›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2019

Resistance to Stress Can Be Experimentally Dissociated From Longevity.

Dylan J Dues, Emily K Andrews, Megan M Senchuk, Jeremy M Van Raamsdonk

Open access · hybridAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-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

32 citing papers in PubMed, 53 citations in OpenAlex.

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  10. Cacao Procyanidins-Induced Lifespan Extension in Caenorhabditis elegans in a Nervous System and CaMKII-Dependent Manner.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  11. Article
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  13. Metabolism, homeostasis, and aging.Trends in endocrinology and metabolism: TEM · 2023
    Review
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  15. Article
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  17. Analysis of aComputational and structural biotechnology journal · 2023
    Article
  18. Article
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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

4 authors at 1 institution in 2 countries.

Dylan J DuesLaboratory of Aging and Neurodegenerative Disease, Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, Michigan.
Emily K AndrewsLaboratory of Aging and Neurodegenerative Disease, Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, Michigan.
Megan M SenchukLaboratory of Aging and Neurodegenerative Disease, Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, Michigan.
Jeremy M Van RaamsdonkLaboratory of Aging and Neurodegenerative Disease, Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, Michigan.
Van Andel Institute · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Molecular mechanisms by which mild elevation of mitochondrial superoxide extends lifespanR01GM121756 · NIGMS · VAN ANDEL RESEARCH INSTITUTE · PI VAN RAAMSDONK, JEREMY MICHAEL · 2017 to 2021
$1.3M
NIGMS NIH HHS R01 GM121756NIH HHS P40 OD010440
6 · The paper itself

Abstract

On the basis of multiple experiments demonstrating that high resistance to stress is associated with long lifespan, it has been proposed that stress resistance is a key determinant of longevity. However, the extent to which high resistance to stress is necessary or sufficient for long life is currently unclear. In this work, we use a genetic approach to disrupt different stress response pathways and examine the resulting effect on the longevity of the long-lived insulin-like growth factor 1 (IGF1) receptor mutant daf-2. Although mutation of the heat shock factor gene hsf-1, deletion of sod genes, deletion of the p38 MAPK kinase gene pmk-1, or deletion of the transcription factor gene egl-27 all resulted in decreased resistance to at least one form of stress and decreased lifespan, the magnitude of change in stress resistance did not correspond to the magnitude of change in lifespan. In addition, we found that deletion of the glycerol-3-phosphate dehydrogenase genes gpdh-1 and gpdh-2 or deletion of the DAF-16 cofactor gene nhl-1 also results in decreased resistance to at least one form of stress but increases lifespan. Overall, our results suggest that while increased stress resistance is associated with longevity, stress resistance, and lifespan can be experimentally dissociated.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDNA-Binding ProteinsGene Expression ProfilingGlycerolphosphate DehydrogenaseLongevityMitogen-Activated Protein KinasesMutationNerve Tissue ProteinsReceptor, IGF Type 1Stress, PhysiologicalSuperoxide DismutaseTranscription FactorsCaenorhabditis elegans ProteinsDNA-Binding ProteinsEGL-27 protein, C elegansGlycerolphosphate Dehydrogenaseheat shock factor-1, C elegansMitogen-Activated Protein KinasesNerve Tissue ProteinsNHL-1 protein, C elegansPmk-1 protein, C elegansReceptor, IGF Type 1Sod-1 protein, C elegansSuperoxide DismutaseTranscription FactorsAgingCaenorhabditis elegansdaf-2GeneticsLifespanStress resistance

Identifiers

PMID30247515
PMCPMC6625593
OpenAlexW2891835498

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.