Evidence map›Paper›PMID 30006559›Full record

ReviewNature reviews. Molecular cell biology2018

Autophagy as a promoter of longevity: insights from model organisms.

Malene Hansen, David C Rubinsztein, David W Walker

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 461 papers.

0numbers the graph read from it
0cells of the map it votes in
461citing papers in PubMed
49.8field-weighted citation impact, top 1% 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

461 citing papers in PubMed, 730 citations in OpenAlex.

  1. Trial
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  7. Review
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  11. Disruption to TFEB signaling and autophagy in newly formed oligodendrocytes leads to aberrant generation of CNS myelin.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Article
  13. Review
  14. Review
  15. Article
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  19. Review
  20. Autophagy: A Double-Edged Sword in the Aging ofInternational journal of molecular sciences · 2026
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 3 countries.

Malene HansenSanford Burnham Prebys Medical Discovery Institute, Program of Development, Aging and Regeneration, La Jolla, CA, USA. mhansen@sbpdiscovery.org.
David C RubinszteinCambridge Institute for Medical Research, Department of Medical Genetics, Cambridge, UK. dcr1000@cam.ac.uk.ORCID 0000-0001-5002-5263
David W WalkerDepartment of Integrative Biology and Physiology, University of California, Los Angeles, CA, USA. davidwalker@ucla.edu.
Sanford Burnham Prebys Medical Discovery Institute · USUK Dementia Research Institute · GBUniversity of California, Los Angeles · US

Funding

Regulation of the Autophagy Process in Organismal AgingR01AG038664 · NIA · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Malene Hansen · 2011 to 2026
$6.4M
Role of Mitochondrial Homeostasis in Animal AgingR01AG037514 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI David W Walker · 2010 to 2026
$5.3M
Metabolic regulation of stem cell behavior and longevityR01AG040288 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JONES, DANA LEANNE, WALKER, DAVID W · 2012 to 2016
$3.0M
Role of Intestinal Homeostasis in Organismal Aging.R01AG049157 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WALKER, DAVID W · 2015 to 2025
$2.4M
Autophagy Regulation by Hippo Kinases STK3/STK4R01GM117466 · NIGMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI HANSEN, MALENE · 2016 to 2019
$1.5M
Medical Research Council UKDRI-2002NIA NIH HHS R01 AG037514NIA NIH HHS R01 AG038664NIA NIH HHS R01 AG040288NIA NIH HHS R01 AG049157NIGMS NIH HHS R01 GM117466Wellcome Trust
6 · The paper itself

Abstract

Autophagy is a conserved process that catabolizes intracellular components to maintain energy homeostasis and to protect cells against stress. Autophagy has crucial roles during development and disease, and evidence accumulated over the past decade indicates that autophagy also has a direct role in modulating ageing. In particular, elegant studies using yeasts, worms, flies and mice have demonstrated a broad requirement for autophagy-related genes in the lifespan extension observed in a number of conserved longevity paradigms. Moreover, several new and interesting concepts relevant to autophagy and its role in modulating longevity have emerged. First, select tissues may require or benefit from autophagy activation in longevity paradigms, as tissue-specific overexpression of single autophagy genes is sufficient to extend lifespan. Second, selective types of autophagy may be crucial for longevity by specifically targeting dysfunctional cellular components and preventing their accumulation. And third, autophagy can influence organismal health and ageing even non-cell autonomously, and thus, autophagy stimulation in select tissues can have beneficial, systemic effects on lifespan. Understanding these mechanisms will be important for the development of approaches to improve human healthspan that are based on the modulation of autophagy.

Identifiers

PMID30006559
PMCPMC6424591
OpenAlexW2883158359

What OpenQuestion holds

Textmetadata
LicenceTDM
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.