Evidence map›Paper›PMID 31929511›Full record

ArticleNature communications2020

Sestrin prevents atrophy of disused and aging muscles by integrating anabolic and catabolic signals.

Jessica Segalés, Eusebio Perdiguero, Antonio L Serrano, Pedro Sousa-Victor, Laura Ortet, Mercè Jardí, Andrei V Budanov, Laura Garcia-Prat, Marco Sandri, David M Thomson and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
8.4field-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

99 citing papers in PubMed, 147 citations in OpenAlex.

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  17. The role of sestrin2 in skeletal muscle regeneration after injury.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
    Article
  18. Review
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  20. 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

39 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

13 authors at 8 institutions in 7 countries.

Jessica SegalésDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Eusebio PerdigueroDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.ORCID http://orcid.org/0000-0003-3529-8989
Antonio L SerranoDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Pedro Sousa-VictorDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Laura OrtetDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Mercè JardíDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Andrei V BudanovSchool of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, D02 R590, Ireland.
Laura Garcia-PratDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain.
Marco SandriDepartment of Biomedical Science, University of Padova, 35100, Padova, Italy.
David M ThomsonDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA.
Michael KarinDepartment of Pharmacology, University of California San Diego, La Jolla, CA, 92093, USA.
Jun Hee LeeDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, 48109-2200, USA.ORCID http://orcid.org/0000-0002-2200-6011
Pura Muñoz-CánovesDepartment of Experimental & Health Sciences, University Pompeu Fabra, CIBERNED, 08003, Barcelona, Spain. pura.munoz@upf.edu.
Universitat Pompeu Fabra · ESBrigham Young University · USTrinity College Dublin · IEUniversity Health Network · CAUniversity of California San Diego · USUniversity of Lisbon · PTUniversity of Michigan · USUniversity of Padua · IT

Funding

The molecular mechanisms of nutrient- and stress-dependent mTORC1 regulation mediated by human Sestrin2.R01DK111465 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHO, UHN-SOO · 2016 to 2020
$2.4M
Mechanisms underlying Hepatoprotective Roles of Sestrin2R01DK102850 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2015 to 2019
$1.7M
Protein inclusions in non-alcoholic steatohepatitisR01DK114131 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JUN HEE · 2018 to 2020
$1.0M
NIDDK NIH HHS R01 DK102850NIDDK NIH HHS R01 DK111465NIDDK NIH HHS R01 DK114131
6 · The paper itself

Abstract

A unique property of skeletal muscle is its ability to adapt its mass to changes in activity. Inactivity, as in disuse or aging, causes atrophy, the loss of muscle mass and strength, leading to physical incapacity and poor quality of life. Here, through a combination of transcriptomics and transgenesis, we identify sestrins, a family of stress-inducible metabolic regulators, as protective factors against muscle wasting. Sestrin expression decreases during inactivity and its genetic deficiency exacerbates muscle wasting; conversely, sestrin overexpression suffices to prevent atrophy. This protection occurs through mTORC1 inhibition, which upregulates autophagy, and AKT activation, which in turn inhibits FoxO-regulated ubiquitin-proteasome-mediated proteolysis. This study reveals sestrin as a central integrator of anabolic and degradative pathways preventing muscle wasting. Since sestrin also protected muscles against aging-induced atrophy, our findings have implications for sarcopenia.

Indexed as

Signal TransductionAgingAnimalsAutophagyDisease Models, AnimalForkhead Box Protein O1Forkhead Box Protein O3Gene ExpressionHeat-Shock ProteinsHumansMaleMechanistic Target of Rapamycin Complex 1MiceMice, Inbred C57BLMice, TransgenicMuscle ProteinsForkhead Box Protein O1Forkhead Box Protein O3Heat-Shock ProteinsMechanistic Target of Rapamycin Complex 1Muscle ProteinsNuclear ProteinsSESN1 protein, humanSESN2 protein, humanSestrins

Identifiers

PMID31929511
PMCPMC6955241
OpenAlexW2999033167

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.