Evidence map›Paper›PMID 41372484›Full record

ArticleBritish journal of cancer2026

ColoStem, a core oncofetal signature that identifies poor prognosis colorectal tumors.

Laura Solé, Eric Canton, María Maqueda, Teresa Lobo-Jarne, Antonio Barbáchano, Ferran Torres, Julia-Jié Cabré-Romans, Ángela Montoto, Lierni Fernández-Ibarrondo, Daniel Martínez-Garcia and 8 more

Abstract read
In one paragraph

Article in British journal of cancer, 2026. 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

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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. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

18 authors.

Laura SoléProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Eric CantonProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
María MaquedaProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Teresa Lobo-JarneProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Antonio BarbáchanoCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain.
Ferran TorresBiostatistics Unit, Medical School, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Julia-Jié Cabré-RomansProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Ángela MontotoProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Lierni Fernández-IbarrondoPathology Department, Hospital del Mar, Barcelona, Spain.
Daniel Martínez-GarciaPathology Department, Hospital del Mar, Barcelona, Spain.
Marta GuixOncology Department, Hospital del Mar, Barcelona, Spain.
Mónica Larrubia-LoringPathology Department, Hospital del Mar, Barcelona, Spain.
Clara MontagutCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain.
Alberto MuñozCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain.ORCID http://orcid.org/0000-0003-3890-4251
Anna BigasProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain.
Mar IglesiasCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain.
Beatriz BellosilloCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain.
Lluís EspinosaProgram in Cancer Research. Hospital del Mar Research Institute, Barcelona, Spain. lespinosa@researchmar.net.ORCID http://orcid.org/0000-0002-2897-4099

Funding

Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) DTS23/00005Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI22/00069
6 · The paper itself

Abstract

backgroundWe have previously shown that non-curative chemotherapy imposes fetal conversion and high metastatic capacity to cancer cells. Analysis of public colorectal cancer datasets confirms the existence of a oncofetal signature consisting of 28 upregulated and 8 downregulated genes that stratify patients with worse prognosis.

methodsWe have generated and analyzed a metacohort which integrates 1118 samples from six colorectal cancer public datasets and performed qPCR analysis of paraffin-embedded and plasma samples from our in-house cohort of colorectal cancer tumors.

resultsWe uncovered a core oncofetal signature, which we have called ColoStem, composed of 5 genes upregulated and 3 genes downregulated that displays prognosis value in a multivariate analysis. We also defined EpiColoStem, a reduction of ColoStem, as a pure epithelial signature with comparable prognosis value as ColoStem. By qPCR analysis of RNA extracted from paraffin-embedded tissues, we demonstrated the actual possibility of using ColoStem and EpiColoStem to refine the prognosis of CRC patients with a simple an affordable method. Initial analysis of plasma samples indicated that both signatures could be adapted for its use in liquid biopsy.

conclusionsOur results reveal ColoStem and EpiColoStem tests as valuable tools for refining patient prognosis through the identification of fetal-type CRC tumors.

Indexed as

Biomarkers, TumorColorectal NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMalePrognosisBiomarkers, Tumor

Identifiers

PMID41372484
PMCPMC12858885

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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.