Evidence map›Paper›PMID 32600387›Full record

ArticleBMC biology2020

The evolutionarily conserved ESRE stress response network is activated by ROS and mitochondrial damage.

Elissa Tjahjono, Aidan P McAnena, Natalia V Kirienko

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Autophagy in Acute Lung Injury.Cell biochemistry and biophysics · 2025
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  14. Article
  15. Innate immunity in C. elegans.Current topics in developmental biology · 2021
    Review
  16. Article
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.

Elissa TjahjonoDepartment of BioSciences, Rice University, 6100 Main St, MS140, Houston, TX, 77005, USA.
Aidan P McAnenaDepartment of BioSciences, Rice University, 6100 Main St, MS140, Houston, TX, 77005, USA.
Natalia V KirienkoDepartment of BioSciences, Rice University, 6100 Main St, MS140, Houston, TX, 77005, USA. kirienko@rice.edu.ORCID 0000-0002-1537-4967
Rice University · US

Funding

Regulation of mitochondrial surveillanceR35GM129294 · NIGMS · RICE UNIVERSITY · PI Natasha Kirienko · 2018 to 2026
$3.6M
Cancer Prevention and Research Institute of Texas RR150044NIGMS NIH HHS R35 GM129294Welch Foundation C-1930
6 · The paper itself

Abstract

backgroundMitochondrial dysfunction causes or contributes to a wide variety of pathologies, including neurodegenerative diseases, cancer, metabolic diseases, and aging. Cells actively surveil a number of mitochondrial readouts to ensure that cellular homeostasis is maintained.

resultsIn this article, we characterize the role of the ethanol and stress response element (ESRE) pathway in mitochondrial surveillance and show that it is robustly activated when the concentration of reactive oxygen species (ROS) in the cell increases. While experiments were mostly performed in Caenorhabditis elegans, we observed similar gene activation profile in human cell lines. The linear relationship between ROS and ESRE activation differentiates ESRE from known mitochondrial surveillance pathways, such as the mitochondrial unfolded protein response (UPR

conclusionThe ESRE pathway responds to mitochondrial damage by monitoring ROS levels. This response is conserved in humans. The ESRE pathway is activated earlier when other mitochondrial surveillance pathways are unavailable during mitochondrial crises, potentially to mitigate stress and restore health. However, the exact mechanisms of pathway activation and crosstalk remain to be elucidated. Ultimately, a better understanding of this network, and its role in the constellation of mitochondrial and cellular stress networks, will improve healthspan.

Indexed as

Signal TransductionAnimalsCaenorhabditis elegansCell LineCell Line, TumorHumansReactive Oxygen SpeciesUnfolded Protein ResponseReactive Oxygen SpeciesESREMitochondriaReductive stressSuperoxideSurveillanceUPRmt

Identifiers

PMID32600387
PMCPMC7322875
OpenAlexW3038192039

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.