Evidence map›Paper›PMID 24747665›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2015

FOXO3 and related transcription factors in development, aging, and exceptional longevity.

Arnold J Kahn

Open access · greenAbstract readConference Proceedings
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  13. Development of the axial skeleton and intervertebral disc.Current topics in developmental biology · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Age-related reduction in the expression of FOXO transcription factors and correlations with intervertebral disc degeneration.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2017
    Article
  18. GH and ageing: Pitfalls and new insights.Best practice & research. Clinical endocrinology & metabolism · 2017
    Review
  19. Article
  20. Healthspan and longevity can be extended by suppression of growth hormone signaling.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
    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

1 author at 1 institution in 1 country.

Arnold J KahnSan Francisco Coordinating Center, California Pacific Medical Center. Buck Institute for Research on Aging, Novato, California. akahn@buckinstitute.org.
Buck Institute for Research on Aging · US

Funding

Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI Thomas Girke, NICHOLAS Joseph SCHORK · 2004 to 2026
$102.6M
NIA NIH HHS U19AG023122
6 · The paper itself

Abstract

In June 2013, a workshop was convened in San Francisco to explore, in depth, the role of the Forkhead transcription factor FOXO3 (and related FOXOs) in development, aging, and, in particular, exceptional longevity. The presentations covered results derived from model systems, computational analysis and bioinformatics, and genomics and genome-wide association studies of a number of cohorts. Although the data collectively strongly reinforce FOXO3 and the FOXO/FOXO3 pathway as very important determinants in aging and life span, much of the detail of how the latter is achieved still remains unknown, in part, because of the very large number of genes (~2,200 in Caenorhabditis elegans) the transcription factor is involved in helping regulate. Particularly challenging at the present time is understanding the association of apparently nonfunctional specific variants (single nucleotide polymorphisms) of FOXO3 and exceptional longevity in humans, a finding replicated in a number of studies. Nonetheless, as summarized in this report, valuable information and insights were presented at the workshop on the transcription factor including but not limited to its role in determining longevity in C elegans and Drosophila (in flies, eg, an important interaction in aging occurs between dFOXO and the transforming growth factor-β/activin pathway), stem cell function and aging (notably in hematopoiesis), downstream regulatory activity (eg, by binding near sites of RNAse occupancy and altering chromatin structure), and as a potential target for the development a healthy aging drug (in this example, using compounds developed and screened to effect FOXO function in cancer cells).

Indexed as

AgingAnimalsBiomarkersEvidence-Based MedicineForkhead Box Protein O3Forkhead Transcription FactorsGenomicsHumansLongevityPhenotypePolymorphism, Single NucleotideSan FranciscoTranscription FactorsTransforming Growth Factor betaBiomarkersForkhead Box Protein O3Forkhead Transcription FactorsFOXO3 protein, humanTranscription FactorsTransforming Growth Factor betaAgingFOXO3LongevityTranscription factor.

Identifiers

PMID24747665
PMCPMC4447793
OpenAlexW2031541868

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.