Evidence map›Paper›PMID 41629132›Full record

ArticleJournal for immunotherapy of cancer2026

Multiomic analysis of colorectal adenocarcinoma reveals a new subtype of myofibroblastic cancer-associated fibroblasts that express high levels of B7-H3 and have poor-prognosis value.

Maelle Picard, Arnaud Guille, Pascal Finetti, Bernadette De Rauglaudre, Nadiya Belfil, Lenaïg Mescam, David Jeremie Birnbaum, François Bertucci, Emilie Mamessier

Abstract read
In one paragraph

Article in Journal for immunotherapy 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, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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.

Maelle PicardAix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.ORCID http://orcid.org/0000-0001-9561-271X
Arnaud GuilleAix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.
Pascal FinettiAix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.ORCID http://orcid.org/0000-0002-2674-3123
Bernadette De RauglaudreDepartment of Digestive Oncology, Hopital La Timone, Aix Marseille Univ, Assistance Publique des Hopitaux de Marseille, Marseille, France.
Nadiya BelfilAix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.
Lenaïg MescamAnatomopathologie, Institut Paoli Calmettes, Marseille, France.
David Jeremie Birnbaum *Aix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.
François Bertucci *Aix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France.ORCID http://orcid.org/0000-0002-0157-0959
Emilie Mamessier *Aix Marseille Univ, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, " Predictive Oncology laboratory", Label "Ligue contre le cancer", Marseille, France emilie.mamessier@inserm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe high mortality rate of patients with colorectal cancer combined with the lack of nontoxic and efficient personalized treatments makes it urgent to develop new targeted therapies for this disease. B7-H3 appears to be a good target, as it is overexpressed in tumor tissue compared with normal tissue. However, B7-H3 is a molecule with ambivalent functions and is expressed by different cell types. This complexity has contributed to the delay in identifying cell subtypes that express B7-H3 and their potential role in colorectal oncogenesis.

methodsIn this integrated multiomics study, we used

resultsWe found that tumors with high

conclusionsWe suggest that anti-B7-H3 immunotherapies might preferentially target cells from the microenvironment rather than tumor cells. This is particularly important for understanding the mode of action of the anti-B7-H3 antibody‒drug conjugate, which is currently being tested in clinical trials in several solid tumors.

Indexed as

AdenocarcinomaB7 AntigensCancer-Associated FibroblastsColorectal NeoplasmsMyofibroblastsBiomarkers, TumorFemaleHumansMultiomicsPrognosisTumor MicroenvironmentB7 AntigensBiomarkers, TumorCD276 protein, humanBiomarkerColorectal CancerImmune Checkpoint InhibitorTumor microenvironment - TME

Identifiers

PMID41629132
PMCPMC12878449

What OpenQuestion holds

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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.