Evidence map›Paper›PMID 41266304›Full record

ArticleCell death & disease2025

Functional analyses and integrated mechanisms of cellular destruction by L-amino acid oxidase.

Krisna Prak, Christin Luft, Eliona Tsefou, Carlos Chávez-Olórtegui, Janos Kriston-Vizi, Robin Ketteler, Vania M M Braga

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Krisna PrakNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Christin LuftLaboratory for Molecular Cell Biology, University College London, London, UK.
Eliona TsefouLaboratory for Molecular Cell Biology, University College London, London, UK.
Carlos Chávez-OlórteguiBiochemistry and Immunology Department, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Janos Kriston-ViziLaboratory for Molecular Cell Biology, University College London, London, UK.
Robin KettelerLaboratory for Molecular Cell Biology, University College London, London, UK.ORCID http://orcid.org/0000-0002-2786-7291
Vania M M BragaNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK. v.braga@imperial.ac.uk.ORCID http://orcid.org/0000-0003-0546-7163

Funding

Wellcome Trust
6 · The paper itself

Abstract

Snakebite accidents are prevalent worldwide and cause a spectrum of severe clinical manifestations and result in a reduction of patient quality of life and economic income. A major bottleneck in envenomation treatment is our limited understanding of how venom toxins perturb specific cellular processes involved in tissue necrosis. Here, we address this knowledge gap and define the cellular mechanisms via which cell death is triggered by the snake toxin L-amino acid oxidase (LAAO). LAAO is a highly toxic enzyme present in various venoms that causes tissue necrosis, edema, coagulopathies, and organ failure. Here, we identify the residues essential for LAAO oxidation and obtain a catalytically inactive LAAO mutant, which is unable to reproduce the cellular phenotypes. Striking cellular defects are triggered by a catalysis-dependent increase in oxidative stress, via H

Indexed as

L-Amino Acid OxidaseAnimalsAutophagyCell DeathHumansHydrogen PeroxideLysosomesMitochondriaMitochondrial DynamicsOxidation-ReductionOxidative StressHydrogen PeroxideL-Amino Acid Oxidase

Identifiers

PMID41266304
PMCPMC12811378

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LicenceCC BY
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Registered trials

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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.