Evidence map›Paper›PMID 39392121›Full record

ArticleJournal of cellular and molecular medicine2024

Reactive oxygen species and aldehyde dehydrogenase 1A as prognosis and theragnostic biomarker in acute myeloid leukaemia patients.

G Venton, J Colle, A Tichadou, J Quessada, C Baier, Y Labiad, M Perez, L De Lassus, M Loosveld, I Arnoux and 4 more

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. 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

14 authors.

G VentonAPHM, Hôpital de la Conception, Service d'Hématologie et Thérapie Cellulaire, Marseille, France.ORCID 0009-0002-4479-7480
J ColleAPHM, Hôpital de la Conception, Service d'Hématologie et Thérapie Cellulaire, Marseille, France.
A TichadouAPHM, Hôpital de la Conception, Service d'Hématologie et Thérapie Cellulaire, Marseille, France.ORCID 0000-0002-1114-6385
J QuessadaAPHM, Hôpital La Timone, Laboratoire d'Hématologie, Marseille, France.
C BaierAdvanced BioDesign, Lyon, France.
Y LabiadAdvanced BioDesign, Lyon, France.
M PerezAdvanced BioDesign, Lyon, France.
L De LassusAPHM, Hôpital de la Conception, Service d'Hématologie et Thérapie Cellulaire, Marseille, France.
M LoosveldAPHM, Hôpital La Timone, Laboratoire d'Hématologie, Marseille, France.ORCID 0000-0002-8372-4148
I ArnouxAPHM, Hôpital La Timone, Laboratoire d'Hématologie, Marseille, France.
N AbbouAPHM, Hopital La Timone, Service d'Oncobiologie, Plateforme M2GM, Hopital de la Timone, Marseille, France.
I CeylanAdvanced BioDesign, Lyon, France.
G MartinAdvanced BioDesign, Lyon, France.
R CostelloAPHM, Hôpital de la Conception, Service d'Hématologie et Thérapie Cellulaire, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukaemia (AML) remains a major unmet medical, despite recent progress in targeted molecular therapies. One aspect of leukaemic cell resistance to chemotherapy is the development of clones with increased capacity to respond to cellular stress and the production of reactive oxygen species (ROS), thanks in particular to a high aldehyde dehydrogenases (ALDH) 1A1/2 activity. At diagnosis, ROS level and ALDH1A1/2 activity in AML patients BM are correlated with the different ELN 2022 prognostic groups and overall survival (OS). A significant lower ALDH1A1/2 activity in BM was observed in the favourable ELN2022 subgroup compared to the intermediate and adverse group (p < 0.01). In the same way, the ROS levels were significantly lower in the favourable ELN 2022 subgroup compared to the intermediate group (p < 0.0001) and adverse group (p < 0.0002). ROS

Indexed as

Aldehyde Dehydrogenase 1 FamilyBiomarkers, TumorLeukemia, Myeloid, AcuteReactive Oxygen SpeciesAdultAgedAged, 80 and overAldehyde DehydrogenaseAldehyde Dehydrogenase, MitochondrialClinical Trials, Phase I as TopicFemaleHumansMaleMiddle AgedMulticenter Studies as TopicPrognosisAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldehyde Dehydrogenase, MitochondrialALDH1A1 protein, humanALDH2 protein, humanBiomarkers, TumorReactive Oxygen SpeciesRetinal Dehydrogenase

Identifiers

PMID39392121
PMCPMC11467733

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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.