Evidence map›Paper›PMID 42265380›Full record

ArticleOncogene2026

CDO1 is a new biomarker to discriminate aggressive forms of prostate cancer.

Jeanne Gaspar Lopes, Angel Markovic, Cécile M Champy, Nicolas Aubourg, Jacques Rr Mathieu, Federica Alberti, Pascale Soyeux-Porte, Kadiatou Drame, Marine Louarn, Thibaud Jamet and 6 more

Abstract read
In one paragraph

Article in Oncogene, 2026. 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

16 authors.

Jeanne Gaspar LopesTRePCa, Univ Paris Est Creteil, Creteil, France.
Angel MarkovicTRePCa, Univ Paris Est Creteil, Creteil, France.
Cécile M ChampyTRePCa, Univ Paris Est Creteil, Creteil, France.
Nicolas AubourgInstitut Mondor de recherche biomédicale (IMRB), Univ Paris Est Creteil, Inserm U955, Créteil, France.
Jacques Rr MathieuINSERM U1279, Gustave Roussy, Villejuif, France; Université Paris Saclay, Villejuif, France.ORCID http://orcid.org/0009-0005-2239-6303
Federica AlbertiTRePCa, Univ Paris Est Creteil, Creteil, France.
Pascale Soyeux-PorteTRePCa, Univ Paris Est Creteil, Creteil, France.
Kadiatou DrameTRePCa, Univ Paris Est Creteil, Creteil, France.
Marine LouarnInstitut Mondor de recherche biomédicale (IMRB), Univ Paris Est Creteil, Inserm U955, Créteil, France.ORCID http://orcid.org/0000-0001-5187-6959
Thibaud JametTRePCa, Univ Paris Est Creteil, Creteil, France.ORCID http://orcid.org/0009-0004-4565-0178
Romain HucTRePCa, Univ Paris Est Creteil, Creteil, France.
Alexandre de la TailleTRePCa, Univ Paris Est Creteil, Creteil, France.
Charles-Antoine DutertreInstitut Mondor de recherche biomédicale (IMRB), Univ Paris Est Creteil, Inserm U955, Créteil, France.
Damien DestouchesTRePCa, Univ Paris Est Creteil, Creteil, France.
Francis VacherotTRePCa, Univ Paris Est Creteil, Creteil, France.
Virginie FirlejTRePCa, Univ Paris Est Creteil, Creteil, France. virginie.firlej@u-pec.fr.ORCID http://orcid.org/0000-0003-4132-0695

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Worldwide, prostate cancer (PCa) ranks second in terms of incidence and eighth in terms of mortality. While most cancers remain silent after initial treatment, some tumors recur. At present, we are unable to predict which patients are at risk of recurrence. In order to determine this risk of recurrence as early as at the biopsy stage, and to enable better therapeutic management of patients, it is essential to identify new biomarkers. In this study, we have demonstrated that Cysteine Dioxygenase CDO1 could be a predictive marker in PCa progression. Transcriptomic analysis showed that CDO1 expression is significantly reduced in patients who have relapsed and lower CDO1 expression is associated with poorer survival outcomes. In PCa, CDO1 expression could be regulated by methylation and androgen signaling pathway. Furthermore, inhibition of CDO1 expression in VCaP prostate cancer cells led to increased cell migration and non-adherent growth. Finally, transcriptomic analysis of these cells with inhibited CDO1 expression demonstrates the complex role of CDO1 and its possible involvement in the mechanisms regulating endoplasmic reticulum stress and protein unfolding. Altogether, these results describe the loss of CDO1 as a marker of aggressiveness in PCa. Furthermore, the loss of CDO1 is thought to be responsible for tumor progression in vitro by acting on multiple signaling pathways.

Indexed as

Biomarkers, TumorCysteine DioxygenaseProstatic NeoplasmsCell Line, TumorCell MovementCell ProliferationDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleNeoplasm Recurrence, LocalPrognosisSignal TransductionBiomarkers, TumorCDO1 protein, humanCysteine Dioxygenase

Identifiers

PMID42265380
PMCPMC13337485

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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.