Evidence map›Paper›PMID 42166218›Full record

ArticleThe journal of pathology. Clinical research2026

Do all colorectal mucinous adenocarcinomas arise via the serrated neoplasia pathway?

Anne-Marie Vos, Peter H van Zwam, Natasja Rutgers, Shannon van Vliet, Elisa Vink-Börger, Rachel S van der Post, Femke Simmer, Iris D Nagtegaal

Abstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Anne-Marie VosDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0003-3926-7282
Peter H van ZwamDepartment of Pathology, Centre for Medical Analysis, Hasselt, Belgium.
Natasja RutgersDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Shannon van VlietDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Elisa Vink-BörgerDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Rachel S van der PostDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Femke SimmerDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Iris D NagtegaalDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.

Funding

Maag Lever Darm Stichting FP 14-10
6 · The paper itself

Abstract

Colorectal mucinous adenocarcinomas (MACs) and serrated adenocarcinomas (SACs) demonstrate considerable overlap in morphological and molecular features, suggesting a spectrum rather than two distinct tumour types. This study investigates the presence of serrated morphological features, precursors, and molecular features in a large cohort of MAC. The study includes 698 MAC collected via the Dutch nationwide pathology databank. Histological review and mismatch repair evaluation were performed on all cases. Next generation sequencing was performed on 396 cases. Multiplex nested methylation-specific PCR (MSP) was performed on 260 microsatellite stable (MSS) cases. The majority of tumours were right-sided (62.6%). Precursor lesions were identified in 9.6% of cases, 88% of which were serrated. Serrated morphology was present in 71% of MAC. Of all cases, 33.8% were microsatellite unstable (MSI). Half of the evaluated cases were CpG island methylator phenotype high. Tumours were divided into six molecular subcategories BRAF/MSS (9.8%), BRAF/MSI (24.7%), KRAS/MSS (38.6%), KRAS/MSI (4.3%), double wild-type/MSS (16.7%), and double wild-type/MSI (5.8%). Based on the presence of a serrated precursor, and/or serrated morphology, and/or a serrated molecular profile, 83.1% of MAC in our cohort could be classified as serrated-MAC. Serrated-MAC developed in older patients, was more often right-sided, showed less perineural invasion, and fewer nodal metastases, when compared to MAC-NOS. Survival analysis showed no significant difference between serrated-MAC and MAC-NOS. We have confirmed that a large majority of colorectal MAC have similar characteristics to SAC.

Indexed as

Adenocarcinoma, MucinousColorectal NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorCpG IslandsDNA MethylationDNA Mismatch RepairFemaleHumansMaleMicrosatellite InstabilityMiddle AgedProto-Oncogene Proteins p21(ras)Biomarkers, TumorKRAS protein, humanProto-Oncogene Proteins p21(ras)colorectal cancermucinous adenocarcinomaserrated adenocarcinomaserrated neoplasia pathway

Identifiers

PMID42166218
PMCPMC13240350

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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.