Evidence map›Paper›PMID 40727998›Full record

ArticleCancer medicine2025

Association Between CD147 Expression, RAS Mutational Status, and Local Recurrence in Resected Locally Advanced Rectal Cancer.

Anaëlle Isnard, Laure-Amandine Cramier, Rémi Vergara, Mehdi Boubaddi, Donatien Fouche, Benjamin Fernandez, Nathalie Senant, Quentin Denost, Éric Rullier, Pierre Dubus and 5 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

15 authors.

Anaëlle IsnardCHU Bordeaux, Tumor Biology and Tumor Bank Laboratory, Pessac, France.
Laure-Amandine CramierSurgical Pathology Department, CHU Bordeaux, Bordeaux, France.
Rémi VergaraSurgical Pathology Department, CHU Bordeaux, Bordeaux, France.
Mehdi BoubaddiBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Donatien FoucheDigestive Surgery Department, CHU Bordeaux, Pessac, France.
Benjamin FernandezBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Nathalie SenantHistopathology Platform, TBM-Core, University of Bordeaux, Bordeaux, France.
Quentin DenostBordeaux Colorectal Institute, Bordeaux, France.
Éric RullierBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Pierre DubusCHU Bordeaux, Tumor Biology and Tumor Bank Laboratory, Pessac, France.
Sandrine DabernatBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Charles DupinBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Véronique VendrelyBRIC (BoRdeaux Institute of onCology), UMR1312, INSERM, University of Bordeaux, Bordeaux, France.
Anne RullierSurgical Pathology Department, CHU Bordeaux, Bordeaux, France.
Samuel AmintasCHU Bordeaux, Tumor Biology and Tumor Bank Laboratory, Pessac, France.ORCID https://orcid.org/0000-0003-3238-5251

Funding

SIRIC-BRIO
6 · The paper itself

Abstract

aimAbout 5% to 10% of rectal cancer (RC) patients experience local disease recurrence after chemoradiotherapy (CRT) and surgery. Identifying patients at high risk of local recurrence (LR) could lead to the personalized management of the patients. Multiple clinicopathological parameters are associated with LR. However, the potential of tumors for local regrowth may partially lie in the expression of pro-tumoral factors and genetic characteristics. In this work, we aimed to evaluate the association of tumor CD147 expression, a well-described cancer aggressiveness biomarker, and mutational status, with post-resection RC LR.

methodsWe retrospectively analyzed all patients experiencing LR after CRT and resection at Bordeaux University Hospital (2010 to 2019) and matched a LR-negative control cohort. CD147 expression was evaluated by immunohistochemistry on post-neoadjuvant treatment residual tumors. Mutational status was assessed by next-generation sequencing. Correlations with LR rates were evaluated.

resultsThe analysis included 29 patients with recurrences and 60 without. The pathological node invasion stage (p = 0.023) and the median number of invaded nodes (p = 0.008) were significantly associated with LR. CD147 expression and mutational status were not associated with LR. Nonetheless, a notable association was observed between RAS mutation and elevated CD147 expression, particularly in male patients (p = 0.005). We confirmed this association in an independent validation cohort of 86 RC patients.

conclusionCD147 tumor expression levels and mutational status do not appear to be associated with resected RC LR. However, the association between RAS mutational status and CD147 expression in male patients tends to confirm the relationship between RAS activating mutations and tumor aggressiveness, as well as their sex-related impact on colorectal tumor biology.

Indexed as

BasiginBiomarkers, TumorMutationNeoplasm Recurrence, LocalRectal NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesBasiginBiomarkers, TumorBSG protein, humanBRAFCD147EMMPRINgenderKRASlocal recurrencerectal cancer

Identifiers

PMID40727998
PMCPMC12305349

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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.