Evidence map›Paper›PMID 39329299›Full record

ArticleJournal of the peripheral nervous system : JPNS2024

Oxygen matters: Unraveling the role of oxygen in the neuronal response to cisplatin.

Jose Crugeiras, Aina Calls, Estefanía Contreras, Montse Alemany, Xavier Navarro, Victor J Yuste, Oriol Casanovas, Esther Udina, Jordi Bruna

Abstract read
In one paragraph

Article in Journal of the peripheral nervous system : JPNS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Jose CrugeirasDepartment of Cell Biology, Physiology, and Immunology, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.ORCID 0009-0008-1564-4462
Aina CallsDepartment of Cell Biology, Physiology, and Immunology, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.
Estefanía ContrerasDepartment of Cell Biology, Physiology, and Immunology, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.
Montse AlemanyUnit of Neuro-Oncology, Hospital Universitari de Bellvitge, Bellvitge Institute for Biomedical Research (IDIBELL), Barcelona, Spain.
Xavier NavarroDepartment of Cell Biology, Physiology, and Immunology, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.
Victor J YusteDepartment of Biochemistry, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.
Oriol CasanovasTumor Angiogenesis Group, ProCURE Program, Catalan Institute of Oncology, OncoBell Program, IDIBELL, Barcelona, Spain.
Esther UdinaDepartment of Cell Biology, Physiology, and Immunology, Institute of Neuroscience, Autonomous University of Barcelona, Bellaterra, Spain.
Jordi BrunaBiomedical Research Center Network on Neurodegenerative Diseases (CIBERNED), Bellaterra, Spain.ORCID 0000-0001-6895-5047

Funding

Instituto de Salud Carlos III
6 · The paper itself

Abstract

BACKGROUND AND

aimsCell culture is a fundamental experimental tool for understanding cell physiology. However, translating these findings to in vivo settings has proven challenging. Replicating donor tissue conditions, including oxygen levels, is crucial for achieving meaningful results. Nevertheless, oxygen culture conditions are often overlooked, particularly in the context of chemotherapy-induced neurotoxicity.

methodsIn this study, we investigated the role of oxygen levels in primary neuronal cultures by comparing neuronal performance under cisplatin exposure (1 μg/mL) in supraphysiological normoxia (representing atmospheric conditions in a standard incubator; 18.5% O

resultsUnder control conditions, both oxygen concentration conditions exhibited similar behaviors. However, after cisplatin administration, sensory neurons cultured under supraphysiological normoxic conditions show higher mortality, exhibit an evolutionarily proinflammatory cytokine profile over time, and activate apoptotic-regulated neuron death markers. In contrast, under physiological conditions, neurons treated with cisplatin exhibited senescence marker expression and an attenuated inflammatory secretome.

interpretationThese results underscore the critical role of oxygen in neuronal culture, particularly in studying compounds where neuronal damage is mechanistically linked to oxidative stress. Even at identical doses of evaluated neurotoxic drugs, distinct cellular phenotypic fates can emerge, impacting translatability to the in vivo setting.

Indexed as

Antineoplastic AgentsCisplatinOxygenAnimalsCells, CulturedCell SurvivalCytokinesNeuronsAntineoplastic AgentsCisplatinCytokinesOxygencell culturechemotherapy‐induced neuropathycisplatinneurotoxicityoxygen

Identifiers

PMID39329299
PMCPMC11625991

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.