Evidence map›Paper›PMID 35584327›Full record

ArticleAmerican journal of physiology. Cell physiology2022

Chaperone-mediated autophagy protects cardiomyocytes against hypoxic-cell death.

Rajeshwary Ghosh, Jennifer Jason Gillaspie, Kenneth S Campbell, J David Symons, Sihem Boudina, James Scott Pattison

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

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  12. Research Progress of Regulatory Cell Death in Coronary Microembolization.International journal of medical sciences · 2025
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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

6 authors at 3 institutions in 1 country.

Rajeshwary GhoshDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota.
Jennifer Jason GillaspieDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota.
Kenneth S CampbellDepartment of Physiology, College of Medicine, University of Kentucky, Lexington, Kentucky.ORCID 0000-0001-5615-5958
J David SymonsDepartment of Nutrition and Integrative Physiology Program in Molecular Medicine, University of Utah, Salt Lake City, Utah.
Sihem BoudinaDepartment of Nutrition and Integrative Physiology Program in Molecular Medicine, University of Utah, Salt Lake City, Utah.
James Scott PattisonDivision of Basic Biomedical Sciences, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota.ORCID 0000-0003-2920-1909
University of South Dakota · USUniversity of Utah · USUniversity of Kentucky · US

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PHILIBERT, INGRID · 2016 to 2025
$42.8M
Dual filament control of myocardial power and hemodynamicsR01HL148785 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI Kenneth S Campbell, Thomas Kampourakis · 2020 to 2026
$3.2M
Length-dependent activation in human myocardiumR01HL149164 · NHLBI · UNIVERSITY OF KENTUCKY · PI CAMPBELL, KENNETH S, TANNER, BERTRAND C.W. · 2020 to 2023
$2.8M
The Role of PRDM16 in Cardiac Development and CardiomyopathyR01HL149870 · NHLBI · UNIVERSITY OF UTAH · PI BOUDINA, SIHEM · 2020 to 2023
$2.8M
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.R01HL141540 · NHLBI · UNIVERSITY OF UTAH · PI SYMONS, JOHN DAVID · 2018 to 2021
$1.7M
NHLBI NIH HHS R01 HL141540NHLBI NIH HHS R01 HL148785NHLBI NIH HHS R01 HL149164NHLBI NIH HHS R01 HL149870NIGMS NIH HHS U54 GM115458
6 · The paper itself

Abstract

Chaperone-mediated autophagy (CMA) is a chaperone-dependent process of selective cytosolic protein turnover that targets specific proteins to lysosomes for degradation. Enhancing protein degradation mechanisms has been shown to be beneficial in multiple models of cardiac disease, including myocardial infarction (MI) and ischemia-reperfusion (I/R) injury. However, the causal role of CMA in cardiomyocyte injury and death is largely unknown. Hypoxia is an important contributor to both MI and I/R damage, which are major, precedent causes of heart failure. Upregulating CMA was hypothesized to protect against hypoxia-induced cardiomyocyte death. Lysosome-associated membrane protein 2a (

Indexed as

Chaperone-Mediated AutophagyHeart FailureApoptosisAutophagyCobaltHumansHypoxiaLysosomal-Associated Membrane Protein 2LysosomesMyocytes, CardiacCobaltcobaltous chlorideLysosomal-Associated Membrane Protein 2cardiomyocytescell deathchaperone-mediated autophagyhypoxiaischemic heart failure

Identifiers

PMID35584327
PMCPMC9829466
OpenAlexW4280559006

What OpenQuestion holds

Textmetadata
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.