Evidence map›Paper›PMID 33113341›Full record

ReviewAnnual review of physiology2021

Sestrins in Physiological Stress Responses.

Myungjin Kim, Allison H Kowalsky, Jun Hee Lee

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  8. Review
  9. The Role of the Gut Microbiota in Vascular Physiology and Health.International journal of molecular sciences · 2025
    Review
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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 1 institution in 1 country.

Myungjin KimDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109, USA; email: myungjin@umich.edu, leeju@umich.edu.
Allison H KowalskyDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109, USA; email: myungjin@umich.edu, leeju@umich.edu.
Jun Hee LeeDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109, USA; email: myungjin@umich.edu, leeju@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RANDY J SEELEY · 2010 to 2026
$20.3M
Research Training in BiogerontologyT32AG000114 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 1985 to 2026
$12.4M
SYTEMS AND INTEGRATIVE BIOLOGYT32GM008322 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOW, MALCOLM JAMES · 1990 to 2020
$5.7M
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
Beneficial effects of Sestrin protein for muscle health during aging and exerciseK01AG061236 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIM, MYUNGJIN · 2019 to 2023
$600k
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
Defining the Sestrin2-AKT signaling pathway, a novel mechanism in the insulin signaling networkF31DK117610 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOWALSKY, ALLISON HO · 2018 to 2019
$73k
NIA NIH HHS K01 AG061236NIA NIH HHS R21 AG045432NIA NIH HHS T32 AG000114NIDDK NIH HHS F31 DK117610NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK102850NIDDK NIH HHS R01 DK111465NIDDK NIH HHS R01 DK114131NIGMS NIH HHS T32 GM008322
6 · The paper itself

Abstract

Sestrins are a family of proteins that respond to a variety of environmental stresses, including genotoxic, oxidative, and nutritional stresses. Sestrins affect multiple signaling pathways: AMP-activated protein kinase, mammalian target of rapamycin complexes, insulin-AKT, and redox signaling pathways. By regulating these pathways, Sestrins are thought to help adapt to stressful environments and subsequently restore cell and tissue homeostasis. In this review, we describe how Sestrins mediate physiological stress responses in the context of nutritional and chemical stresses (liver), physical movement and exercise (skeletal muscle), and chemical, physical, and inflammatory injuries (heart). These findings also support the idea that Sestrins are a molecular mediator of hormesis, a paradoxical beneficial effect of low- or moderate-level stresses in living organisms.

Indexed as

AnimalsExerciseHomeostasisHumansMuscle, SkeletalSestrinsSignal TransductionStress, PhysiologicalSestrinsagingcolonexercisehormesislivermuscleobesitySestrinstress response

Identifiers

PMID33113341
PMCPMC7878365
OpenAlexW3096511936

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.