Evidence map›Paper›PMID 24055102›Full record

ReviewCell metabolism2013

Sestrins orchestrate cellular metabolism to attenuate aging.

Jun Hee Lee, Andrei V Budanov, Michael Karin

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Cell metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07370363 (Effects of Moderate-Intensity Continuous Exercise Versus Brisk Interval Exercise on Cardiometabolic Parameters and Sestrin-2 Levels in Hypertensive Obese Women), which is not on this map. Cited by 198 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
198citing papers in PubMed, 3 pooled it
9.1field-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.

NCT07370363 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Effects of Moderate-Intensity Continuous Exercise Versus Brisk Interval Exercise on Cardiometabolic Parameters and Sestrin-2 Levels in Hypertensive Obese Women: A Randomized Controlled Trial

TypeinterventionalSponsorHavva Talay ÇalışRan2026 to 2026Enrolled42ConditionsObesity, HypertensionArmsModerate-Intensity Continuous Exercise, Brisk Interval Exercise
3 · Its place in the literature

Who cites it

198 citing papers in PubMed, 3 syntheses or guidelines pooled it, 344 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Guideline
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. A viral Cyclin D homolog protein hijacks the metabolic stress sensor SESN2 to promote primary effusion lymphoma growth.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Article
  19. Article
  20. Article

138 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

3 authors at 3 institutions in 1 country.

Jun Hee Lee *Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48109, USA.
Andrei V Budanov *Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Michael KarinLaboratory of Gene Regulation and Signal Transduction, Departments of Pharmacology and Pathology University of California, San Diego, San Diego, CA 92093, USA.
University of California, San Diego · USUniversity of Michigan–Ann Arbor · USVirginia Commonwealth University · US

Funding

Yeast Genetics and Stress Response Genes-BiomedicalP42ES010337 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUKEY, ROBERT H · 2000 to 2022
$69.8M
Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Neil Alexander · 2004 to 2026
$29.2M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joyce Lee · 2010 to 2026
$20.3M
Research DevelopmentP30AG013283 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MILLER, RICHARD A · 1995 to 2014
$12.3M
Role of Inflammation in tumor promotion and progressionR01CA118165 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KARIN, MICHAEL · 2007 to 2016
$4.6M
TOR signaling and autophagy in obesity-promoted liver tumorigenesisR01CA155120 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KARIN, MICHAEL · 2011 to 2015
$1.9M
The Role of p53-inducible Sesn1 and Sesn2 genes in lung carcinogenesisR01CA172660 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GROSSMAN, STEVEN R. · 2013 to 2017
$1.5M
Sestrin1-knockout mice as a model of facilitated muscle agingR21AG045432 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2013 to 2014
$428k
Role of p53 and the p53-inducible Sestrin1 and 2 genes in hepatocarcinogenesisK99DK082080 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BUDANOV, ANDREI VLADIMIROVICH · 2008 to 2009
$156k
NCI NIH HHS CA118165NCI NIH HHS CA155120NCI NIH HHS CA172660NCI NIH HHS R01 CA118165NCI NIH HHS R01 CA155120NCI NIH HHS R01 CA172660NIA NIH HHS AG045432NIA NIH HHS P30 AG013283NIA NIH HHS P30-AG013283NIA NIH HHS P30 AG024824NIA NIH HHS P30-AG024824NIA NIH HHS R21 AG045432NIDDK NIH HHS DK082080NIDDK NIH HHS K99 DK082080NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK089503NIDDK NIH HHS P30-DK089503NIEHS NIH HHS P42 ES010337NIEHS NIH HHS P42-ES010337
6 · The paper itself

Abstract

The Sestrins constitute a family of evolutionarily conserved stress-inducible proteins that suppress oxidative stress and regulate AMP-dependent protein kinase (AMPK)-mammalian target of rapamycin (mTOR) signaling. By virtue of these activities, the Sestrins serve as important regulators of metabolic homeostasis. Accordingly, inactivation of Sestrin genes in invertebrates resulted in diverse metabolic pathologies, including oxidative damage, fat accumulation, mitochondrial dysfunction, and muscle degeneration, that resemble accelerated tissue aging. Likewise, Sestrin deficiencies in mice led to accelerated diabetic progression upon obesity. Further investigation of Sestrin function and regulation should provide new insights into age-associated metabolic diseases, such as diabetes, myopathies, and cancer.

Indexed as

AgingAMP-Activated Protein KinasesAnimalsMitochondriaNeoplasmsNuclear ProteinsObesityOxidative StressSignal TransductionTOR Serine-Threonine KinasesAMP-Activated Protein KinasesNuclear ProteinsTOR Serine-Threonine Kinases

Identifiers

PMID24055102
PMCPMC3858445
OpenAlexW2014267867

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.