Evidence map›Paper›PMID 26525455›Full record

ReviewCold Spring Harbor perspectives in medicine2015

Biochemical Genetic Pathways that Modulate Aging in Multiple Species.

Alessandro Bitto, Adrienne M Wang, Christopher F Bennett, Matt Kaeberlein

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing 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

66 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Sirt6 protects retinal ganglion cells and optic nerve from degeneration during aging and glaucoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  11. Review
  12. Use of Farnesyl Transferase Inhibitors in an Ageing Model inJournal of developmental biology · 2023
    Article
  13. Article
  14. Identifying lipid particle sub-types in liveFrontiers in chemistry · 2023
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. New Roles for MicroRNAs in Old Worms.Frontiers in aging · 2022
    Review
  20. Article

6 more citing papers are in PubMed but not listed here.

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.

Alessandro BittoDepartment of Pathology, University of Washington, Seattle, Washington 98195.
Adrienne M WangDepartment of Pathology, University of Washington, Seattle, Washington 98195.
Christopher F BennettDepartment of Pathology, University of Washington, Seattle, Washington 98195.
Matt KaeberleinDepartment of Pathology, University of Washington, Seattle, Washington 98195.

Funding

SPECIFICITY OF OXYGEN DNA DAMAGE AND MUTAGENESISP01AG001751 · NIA · UNIVERSITY OF WASHINGTON · PI PRUSKY, GLEN THOMAS · 1985 to 2021
$29.6M
TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
GENETIC APPROACHES TO AGING RESEARCHT32AG000057 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 1985 to 2019
$14.2M
Environmetal Pathology/Toxicology Training ProgramT32ES007032 · NIEHS · UNIVERSITY OF WASHINGTON · PI FAUSTMAN, ELAINE M, ROSENFELD, MICHAEL E · 1985 to 2023
$10.7M
Mechanism of lifespan and healthspan regulation by the hypoxic response transcripR01AG038518 · NIA · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT · 2011 to 2015
$1.5M
Endocrine Regulation of Survival Responses in C. elegansR01AG033598 · NIA · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT · 2010 to 2014
$1.5M
Defining the Mechanisms of genotype-dependent responses to caloric restrictionR01AG039390 · NIA · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT · 2011 to 2015
$1.5M
NIA NIH HHS AG033598NIA NIH HHS AG038518NIA NIH HHS AG039390NIA NIH HHS P01 AG001751NIA NIH HHS R01 AG033598NIA NIH HHS R01 AG038518NIA NIH HHS R01 AG039390NIA NIH HHS T32 AG000057NIA NIH HHS T32AG000057NIEHS NIH HHS T32 ES007032NIEHS NIH HHS T32ES007032NIGMS NIH HHS T32 GM007270
6 · The paper itself

Abstract

The mechanisms underlying biological aging have been extensively studied in the past 20 years with the avail of mainly four model organisms: the budding yeast Saccharomyces cerevisiae, the nematode Caenorhabditis elegans, the fruitfly Drosophila melanogaster, and the domestic mouse Mus musculus. Extensive research in these four model organisms has identified a few conserved genetic pathways that affect longevity as well as metabolism and development. Here, we review how the mechanistic target of rapamycin (mTOR), sirtuins, adenosine monophosphate-activated protein kinase (AMPK), growth hormone/insulin-like growth factor 1 (IGF-1), and mitochondrial stress-signaling pathways influence aging and life span in the aforementioned models and their possible implications for delaying aging in humans. We also draw some connections between these biochemical pathways and comment on what new developments aging research will likely bring in the near future.

Indexed as

AgingAnimalsCaenorhabditis elegansDrosophila melanogasterLongevityMiceModels, BiologicalSaccharomyces cerevisiae

Identifiers

PMID26525455
PMCPMC4632857

What OpenQuestion holds

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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.