Evidence map›Paper›PMID 22936916›Full record

ArticleFrontiers in physiology2012

Integration of peroxisomes into an endomembrane system that governs cellular aging.

Adam Beach, Michelle T Burstein, Vincent R Richard, Anna Leonov, Sean Levy, Vladimir I Titorenko

Abstract read
In one paragraph

Article in Frontiers in physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Metabolomic Profiling ofJournal of fungi (Basel, Switzerland) · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Peroxisomes in host defense.PLoS pathogens · 2020
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Protective Effect of the Hexanic Extract ofAntioxidants (Basel, Switzerland) · 2019
    Article
  12. Article
  13. Article
  14. Some Metabolites Act as Second Messengers in Yeast Chronological Aging.International journal of molecular sciences · 2018
    Review
  15. Article
  16. Article
  17. Pex35 is a regulator of peroxisome abundance.Journal of cell science · 2017
    Article
  18. Review
  19. Article
  20. Autophagic degradation of peroxisomes in mammals.Biochemical Society transactions · 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

6 authors.

Adam BeachDepartment of Biology, Concordia University, Montreal PQ, Canada.
Michelle T Burstein
Vincent R Richard
Anna Leonov
Sean Levy
Vladimir I Titorenko

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The peroxisome is an organelle that has long been known for its essential roles in oxidation of fatty acids, maintenance of reactive oxygen species (ROS) homeostasis and anaplerotic replenishment of tricarboxylic acid (TCA) cycle intermediates destined for mitochondria. Growing evidence supports the view that these peroxisome-confined metabolic processes play an essential role in defining the replicative and chronological age of a eukaryotic cell. Much progress has recently been made in defining molecular mechanisms that link cellular aging to fatty acid oxidation, ROS turnover, and anaplerotic metabolism in peroxisomes. Emergent studies have revealed that these organelles not only house longevity-defining metabolic reactions but can also regulate cellular aging via their dynamic communication with other cellular compartments. Peroxisomes communicate with other organelles by establishing extensive physical contact with lipid bodies, maintaining an endoplasmic reticulum (ER) to peroxisome connectivity system, exchanging certain metabolites, and being involved in the bidirectional flow of some of their protein and lipid constituents. The scope of this review is to summarize the evidence that peroxisomes are dynamically integrated into an endomembrane system that governs cellular aging. We discuss recent progress in understanding how communications between peroxisomes and other cellular compartments within this system influence the development of a pro- or anti-aging cellular pattern. We also propose a model for the integration of peroxisomes into the endomembrane system governing cellular aging and critically evaluate several molecular mechanisms underlying such integration.

Indexed as

autophagycellular aginginterorganellar communicationorganelle inheritanceperoxisomeproteostasissenescence factorssirtuins

Identifiers

PMID22936916
PMCPMC3424522

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.