Evidence map›Paper›PMID 40594269›Full record

ArticleScientific reports2025

Characterization of collagen profile in peritoneal metastases of colorectal cancer.

P Villarejo-Campos, S García Gómez-Heras, S González-Moreno, S Qian Zhang, R Franco-Rodríguez, I Díaz-Caro, R Olivera-Salazar, D García-Olmo, M García-Arranz

Abstract read
In one paragraph

Article in Scientific reports, 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

9 authors.

P Villarejo-Campos *Department of Surgery, Fundación Jiménez Díaz University Hospital, Avda. Reyes Católicos, 2, 28040, Madrid, Spain. pedro.villarejo@quironsalud.es.
S García Gómez-Heras *Department of Basic Health Science, Faculty of Health Sciences, Rey Juan Carlos University, 28922, Alcorcón, Madrid, Spain.
S González-MorenoDepartment of Surgical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain.
S Qian ZhangDepartment of Surgery, Fundación Jiménez Díaz University Hospital, Avda. Reyes Católicos, 2, 28040, Madrid, Spain.
R Franco-RodríguezDepartment of Basic Health Science, Faculty of Health Sciences, Rey Juan Carlos University, 28922, Alcorcón, Madrid, Spain.
I Díaz-CaroDepartment of Nursing, Gregorio Marañón University Hospital, Madrid, Spain.
R Olivera-SalazarNew Therapies Laboratory, Health Research Institute-Fundación Jiménez Díaz University Hospital (IIS-FJD), Avda. Reyes Católicos, 2, 28040, Madrid, Spain.
D García-OlmoDepartment of Surgery, Fundación Jiménez Díaz University Hospital, Avda. Reyes Católicos, 2, 28040, Madrid, Spain.
M García-ArranzDepartment of Surgery, Universidad Autónoma de Madrid, C/Arzobispo Morcillo S/N, 28034, Madrid, Spain.

Funding

Instituto de Salud Carlos III (ISCIII) and co-funded by the European Union DTS22/00048
6 · The paper itself

Abstract

The tumor microenvironment (TME) plays a critical role in cancer progression and response to treatment. In colorectal cancer (CRC), a collagen-rich extracellular matrix (ECM) is a well-established feature of primary tumors and liver metastases. However, the composition of the ECM in peritoneal metastases remains poorly characterized. In this descriptive study, we analyzed the histological distribution of four major collagen types (I, II, III, and IV) in peritoneal metastases from 39 CRC patients using immunohistochemical techniques. Type III fibrillar collagen was predominant, showing moderate to high expression in 80 percent of cases, followed by type IV collagen in 56 percent. Type I collagen demonstrated low intensity in 64 percent of cases. Notably, type II collagen, typically restricted to cartilaginous tissues, was also detected within the tumor stroma, an unexpected finding given its usual absence in this histological contex. These results highlight the unique collagen-rich stroma in CRC peritoneal metastases, dominated by types III and IV collagen, and identify type II collagen as a novel component. This study provides new insight into the stromal architecture of CRC peritoneal metastases and may serve as a foundation for future research on collagen-targeted therapeutic strategies.

Indexed as

CollagenColorectal NeoplasmsPeritoneal NeoplasmsAdultAgedAged, 80 and overCollagen Type IExtracellular MatrixFemaleHumansImmunohistochemistryMaleMiddle AgedTumor MicroenvironmentCollagenCollagen Type I

Identifiers

PMID40594269
PMCPMC12218282

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