Loss of the epithelial marker CDX1 predicts poor prognosis in early-stage CRC patients.

CDX1 Colorectal cancer Fetal conversion Patient prognosis

Journal

Biochimica et biophysica acta. Molecular cell research
ISSN: 1879-2596
Titre abrégé: Biochim Biophys Acta Mol Cell Res
Pays: Netherlands
ID NLM: 101731731

Informations de publication

Date de publication:
10 Jan 2024
Historique:
received: 17 10 2023
revised: 18 12 2023
accepted: 03 01 2024
medline: 13 1 2024
pubmed: 13 1 2024
entrez: 12 1 2024
Statut: aheadofprint

Résumé

We have previously shown that non-curative chemotherapy imposes fetal conversion and high metastatic capacity to cancer cells. From the set of genes differentially expressed in Chemotherapy Resistant Cells, we obtained a characteristic fetal intestinal cell signature that is present in a group of untreated tumors and is sufficient to predict patient prognosis. A feature of this fetal signature is the loss of CDX1. We have analyzed transcriptomic data in public datasets and performed immunohistochemistry analysis of paraffin embedded tumor samples from two cohorts of colorectal cancer patients. We demonstrated that low levels of CDX1 are sufficient to identify patients with poorest outcome at the early tumor stages II and III. Presence tumor areas that are negative for CDX1 staining in stage I cancers is associated with tumor relapse. Our results reveal the actual possibility of incorporating CDX1 immunostaining as a valuable biomarker for CRC patients.

Sections du résumé

BACKGROUND BACKGROUND
We have previously shown that non-curative chemotherapy imposes fetal conversion and high metastatic capacity to cancer cells. From the set of genes differentially expressed in Chemotherapy Resistant Cells, we obtained a characteristic fetal intestinal cell signature that is present in a group of untreated tumors and is sufficient to predict patient prognosis. A feature of this fetal signature is the loss of CDX1.
METHODS METHODS
We have analyzed transcriptomic data in public datasets and performed immunohistochemistry analysis of paraffin embedded tumor samples from two cohorts of colorectal cancer patients.
RESULTS RESULTS
We demonstrated that low levels of CDX1 are sufficient to identify patients with poorest outcome at the early tumor stages II and III. Presence tumor areas that are negative for CDX1 staining in stage I cancers is associated with tumor relapse.
CONCLUSIONS CONCLUSIONS
Our results reveal the actual possibility of incorporating CDX1 immunostaining as a valuable biomarker for CRC patients.

Identifiants

pubmed: 38216091
pii: S0167-4889(24)00001-6
doi: 10.1016/j.bbamcr.2024.119658
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

119658

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Laura Solé (L)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.

Teresa Lobo-Jarne (T)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.

Júlia-Jié Cabré-Romans (JJ)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.

Antón González (A)

Pathology Department, Hospital del Mar, Barcelona, Spain.

Lierni Fernandez (L)

Pathology Department, Hospital del Mar, Barcelona, Spain.

Laura Marruecos (L)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; The Walter and Eliza Hall Institute, Melbourne, Australia.

Marta Guix (M)

Oncology Department, Hospital del Mar, Barcelona, Spain.

Miriam Cuatrecasas (M)

Pathology Department, Centre of Biomedical Diagnosis (CDB), Hospital Clinic, 08036 Barcelona, Spain; Centro de Investigacion Biomedica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), 28029 Madrid, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Sandra López (S)

Pathology Department, Centre of Biomedical Diagnosis (CDB), Hospital Clinic, 08036 Barcelona, Spain; Centro de Investigacion Biomedica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), 28029 Madrid, Spain.

Beatriz Bellosillo (B)

Pathology Department, Hospital del Mar, Barcelona, Spain.

Ferran Torres (F)

Biostatistics Unit, Medical School, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.

Mar Iglesias (M)

Pathology Department, Hospital del Mar, Barcelona, Spain; Centro de Investigacion Biomedica en Red Cancer (CIBERONC), Madrid, Spain.

Anna Bigas (A)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; Centro de Investigacion Biomedica en Red Cancer (CIBERONC), Madrid, Spain; Josep Carreras Leukemia Research Institute, Barcelona, Spain.

Lluís Espinosa (L)

Program in Cancer Research, Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; Centro de Investigacion Biomedica en Red Cancer (CIBERONC), Madrid, Spain. Electronic address: lespinosa@imim.es.

Classifications MeSH