Evidence map›Paper›PMID 20965426›Full record

ReviewMolecular cell2010

The aging stress response.

Marcia C Haigis, Bruce A Yankner

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 273 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
273citing papers in PubMed, 1 pooled it
10.4field-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

273 citing papers in PubMed, 1 synthesis or guideline pooled it, 510 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  12. Review
  13. Suppression rather than activation of the integrated stress response (GCN2-ATF4) pathway extends lifespan in the fly.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. Review
  16. Immune Aging as a Failure of Programmed Cell Death Coordination.International journal of molecular sciences · 2026
    Review
  17. Article
  18. Article
  19. Article
  20. Article

213 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

2 authors at 1 institution in 1 country.

Marcia C HaigisDepartment of Pathology, Harvard Medical School, Boston, MA 02115, USA. marcia_haigis@hms.harvard.edu
Bruce A Yankner
Harvard University · US

Funding

THE ROLE OF Cdk5 IN THE DNA DAMAGE RESPONCE DURING AGING AND NEURODEGENERATIONP01AG027916 · NIA · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2006 to 2010
$7.7M
Modeling the Aging EpigenomeDP1AG044161 · NIA · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2012 to 2014
$2.5M
Regulation of mitochondrial metabolism by SIRT4R01AG032375 · NIA · HARVARD MEDICAL SCHOOL · PI HAIGIS, MARCIA · 2009 to 2014
$1.8M
Modeling the Aging EpigenomeDP1OD006849 · OD · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2010 to 2011
$1.7M
Gene Regulation and DNA Damage in the Aging BrainR01AG026651 · NIA · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2005 to 2009
$1.7M
Epigenetic Analysis of iPS Cell Models of Aging and Alzheimer's DiseaseRC1AG036106 · NIA · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2009 to 2010
$1.0M
NIA NIH HHS AG032375NIA NIH HHS AG036106NIA NIH HHS AG26651NIA NIH HHS AG27916NIA NIH HHS DP1 AG044161NIA NIH HHS P01 AG027916NIA NIH HHS R01 AG026651NIA NIH HHS R01 AG032375NIA NIH HHS RC1 AG036106NIH HHS DP1 OD006849
6 · The paper itself

Abstract

Aging is the outcome of a balance between damage and repair. The rate of aging and the appearance of age-related pathology are modulated by stress response and repair pathways that gradually decline, including the proteostasis and DNA damage repair networks and mitochondrial respiratory metabolism. Highly conserved insulin/IGF-1, TOR, and sirtuin signaling pathways in turn control these critical cellular responses. The coordinated action of these signaling pathways maintains cellular and organismal homeostasis in the face of external perturbations, such as changes in nutrient availability, temperature, and oxygen level, as well as internal perturbations, such as protein misfolding and DNA damage. Studies in model organisms suggest that changes in signaling can augment these critical stress response systems, increasing life span and reducing age-related pathology. The systems biology of stress response signaling thus provides a new approach to the understanding and potential treatment of age-related diseases.

Indexed as

Signal TransductionAgingAnimalsCellular SenescenceHumansModels, BiologicalNeoplasmsNeurodegenerative DiseasesOxidative StressStress, Physiological

Identifiers

PMID20965426
PMCPMC2987618
OpenAlexW2043304304

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.