Evidence map›Paper›PMID 22509016›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Midlife gene expressions identify modulators of aging through dietary interventions.

Bing Zhou, Liu Yang, Shoufeng Li, Jialiang Huang, Haiyang Chen, Lei Hou, Jinbo Wang, Christopher D Green, Zhen Yan, Xun Huang and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

39 citing papers in PubMed, 69 citations in OpenAlex.

  1. The Extended Lifespan ofCurrent issues in molecular biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The landscape of aging.Science China. Life sciences · 2022
    Review
  10. Article
  11. Oxidative medicine and cellular longevity · 2022
    Article
  12. Article
  13. Antiaging Effects ofOxidative medicine and cellular longevity · 2021
    Article
  14. Article
  15. Rosy Beginnings: Studying Peroxisomes inFrontiers in cell and developmental biology · 2020
    Review
  16. Review
  17. Article
  18. Article
  19. Peroxisomes in Immune Response and Inflammation.International journal of molecular sciences · 2019
    Review
  20. 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

15 authors at 5 institutions in 2 countries.

Bing ZhouChinese Academy of Sciences Key Laboratory for Computational Biology, Chinese Academy of Sciences-Max Planck Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Liu Yang
Shoufeng Li
Jialiang Huang
Haiyang Chen
Lei Hou
Jinbo Wang
Christopher D Green
Zhen Yan
Xun Huang
Matt Kaeberlein
Li Zhu
Huasheng Xiao
Yong Liu
Jing-Dong J Han
Chinese Academy of Sciences · CNShanghai Institutes for Biological Sciences · CNInstitute of Genetics and Developmental Biology · CNUniversity of Virginia · USUniversity of Washington · US

Funding

p38 MAPK a regulator of muscle contraction and functionR01AR050429 · NIAMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI YAN, ZHEN · 2005 to 2022
$5.3M
NIAMS NIH HHS R01 AR050429
6 · The paper itself

Abstract

Dietary interventions are effective ways to extend or shorten lifespan. By examining midlife hepatic gene expressions in mice under different dietary conditions, which resulted in different lifespans and aging-related phenotypes, we were able to identify genes and pathways that modulate the aging process. We found that pathways transcriptionally correlated with diet-modulated lifespan and physiological changes were enriched for lifespan-modifying genes. Intriguingly, mitochondrial gene expression correlated with lifespan and anticorrelated with aging-related pathological changes, whereas peroxisomal gene expression showed an opposite trend. Both organelles produce reactive oxygen species, a proposed causative factor of aging. This finding implicates a contribution of peroxisome to aging. Consistent with this hypothesis, lowering the expression levels of peroxisome proliferation genes decreased the cellular peroxide levels and extended the lifespan of Drosophila melanogaster and Caenorhabditis elegans. These findings show that transcriptional changes resulting from dietary interventions can effectively reflect causal factors in aging and identify previously unknown or under-appreciated longevity pathways, such as the peroxisome pathway.

Indexed as

DietGene Expression ProfilingAgingAnimalsCaenorhabditis elegansCluster AnalysisDrosophila melanogasterEnergy MetabolismFemaleHydrogen PeroxideLongevityMaleMiceMice, Inbred C57BLMicroscopy, Electron, TransmissionMitochondria, LiverHydrogen PeroxideReactive Oxygen Species

Identifiers

PMID22509016
PMCPMC3358859
OpenAlexW2167492383

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.