Evidence map›Paper›PMID 27298226›Full record

ArticleVirchows Archiv : an international journal of pathology2016

MUC1, MUC2, MUC5AC, and MUC6 in colorectal cancer: expression profiles and clinical significance.

Johannes Betge, Nora I Schneider, Lars Harbaum, Marion J Pollheimer, Richard A Lindtner, Peter Kornprat, Matthias P Ebert, Cord Langner

Open access · hybridAbstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 3 pooled it
7.0field-weighted citation impact, top 3% of its field
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

87 citing papers in PubMed, 3 syntheses or guidelines pooled it, 140 citations in OpenAlex.

  1. Pooled it
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  20. Diagnostic gastrointestinal markers in primary lung cancer and pulmonary metastases.Virchows Archiv : an international journal of pathology · 2024
    Article

27 more citing papers are in PubMed but not listed here.

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

8 authors at 5 institutions in 2 countries.

Johannes BetgeDepartment of Medicine II, University Hospital Mannheim, Medical Faculty Mannheim: Heidelberg University, Mannheim, Germany.
Nora I SchneiderInstitute of Pathology, Medical University of Graz, Auenbruggerplatz 25, 8036, Graz, Austria.
Lars HarbaumDepartment of Medicine II, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Marion J PollheimerInstitute of Pathology, Medical University of Graz, Auenbruggerplatz 25, 8036, Graz, Austria.
Richard A LindtnerDepartment of Surgery, Medical University of Innsbruck, Innsbruck, Austria.
Peter KornpratDepartment of Surgery, Division of General Surgery, Medical University of Graz, Graz, Austria.
Matthias P EbertDepartment of Medicine II, University Hospital Mannheim, Medical Faculty Mannheim: Heidelberg University, Mannheim, Germany.
Cord LangnerInstitute of Pathology, Medical University of Graz, Auenbruggerplatz 25, 8036, Graz, Austria. cord.langner@medunigraz.at.
Medical University of Graz · ATHeidelberg University · DEUniversität Hamburg · DEUniversität Innsbruck · ATUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucin glycoprotein expression can be altered during the carcinogenic process. The impact on the prognosis of patients with colorectal cancer (CRC) is controversial. We analyzed tumors from 381 patients for MUC1, MUC2, MUC5AC, and MUC6 expression by immunohistochemical staining, using tissue microarrays. Progression-free and cancer-specific survival were determined using the Kaplan-Meier method. Expression of intestinal mucin MUC2 was lost in 85 (23 %) CRCs, and patients with MUC6-negative tumors showed shorter progression-free survival (PFS, p = 0.043). Gastric mucins MUC5AC and MUC6 showed high (>50 %) aberrant expression in 28 (8 %) and 9 (2 %) cases, respectively. High expression of MUC5AC was associated with longer PFS (p = 0.055). High expression of MUC6 was associated with 100 % PFS (p = 0.024) and longer cancer-specific survival (CSS, p = 0.043). MUC1 was expressed in 238 (64 %) tumors and had no impact on outcome. When analysis was restricted to stages II and III, loss of MUC2 was associated with adverse outcome. Overexpression of both MUC5AC and MUC6 significantly predicted favorable PFS and CSS. In conclusion, loss of MUC2 expression proved to be a predictor of adverse outcome, while the gain of aberrant expression of MUC5AC and particularly of MUC6 was associated with favorable outcome in CRC, notably in intermediate stages II and III.

Indexed as

AdultAgedAged, 80 and overAntigens, NeoplasmBiomarkers, TumorColorectal NeoplasmsFemaleHumansImmunohistochemistryMaleMiddle AgedMucin-1Mucin-2Mucin 5ACMucin-6PrognosisAntigens, NeoplasmBiomarkers, TumorMUC2 protein, humanMUC6 protein, humanMucin-1Mucin-2Mucin 5ACMucin-6ImmunohistochemistryLarge intestineMucinPrognosisPrognostic factorStage II

Identifiers

PMID27298226
PMCPMC5007278
OpenAlexW2431979144

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LicenceCC BY
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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.