Cited by 132Glycosylation and Glycoproteins ResearchGenetic factors in colorectal cancerDigestive system and related health

Expression of MUC2‐mucin in colorectal adenomas and carcinomas of different histological types

Blank, Monika, Klussmann, Enno, Krüger‐Krasagakes, Sabine, Schmitt‐Gräff, Anette, Stolte, Manfred, Bornhoeft, Gudrun, Stein, Harald, Xing, Pei‐Xiang +4 more·1994·International Journal of Cancer

Abstract

The expression of mucin MUC2 was investigated in normal colonic tissue, in colonic adenomas and in carcinomas of the mucinous and non‐mucinous type. The latter were subdivided into carcinomas originating from the adenoma‐carcinoma sequence (ACS) and de novo (DN) carcinomas. The expression was assayed by immunohistochemistry with the monoclonal anti‐MUC2 antibody CCP58 and by mRNA semiquantitation. MUC2 protein epitope CCP58 was strongly expressed in 21 % of normal colonic tissues, in 40% of villous and in 48% of tubular adenomas. Mucinous carcinomas exhibited strong expression in 72%, ACS carcinomas in 21 % and DN adenocarcinomas in none of the tumors investigated. Compared with the adjacent non malignant tissue (transitional mucosa), CCP58 epitope expression in the tumor was higher in 74% of mucinous carcinomas, but equal or lower in 69% of ACS carcinomas and in 100% of de novo carcinomas. The alterations of MUC2 expression detected by immunohistochemistry in adenocarcinomas were confirmed on mRNA level. These data indicate that the MUC2 expression pattern is different in the 3 carcinoma types investigated. MUC2 over‐expression occurs in the adenomatous tissue. It is always maintained in mucinous carcinomas, but frequently decreased in non‐mucinous ACS carcinomas. DN carcinomas are most frequently associated with decreased expression of MUC2. © 1994 Wiley‐Liss, Inc.

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Crossref · 10.1002/ijc.2910590302

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References 28 · Cited by 132

Authors
Blank, M., Klussmann, E., Krüger‐Krasagakes, S., Schmitt‐Gräff, A., Stolte, M., Bornhoeft, G., Stein, H., Xing, P., McKenzie, I. F. C., Verstijnen, C. P. H. J., Riecken, E. O., & Hanski, C.
Affiliations
  • Freie Universität Berlin (DE)
  • Bayreuth Medical Center (DE)
Corresponding author
Hanski, Christoph
Venue
International Journal of Cancer
Publisher
Wiley
Published
1994-11
Volume
59
Issue
3
Pages
301-306
ISSN
  • 0020-7136 (ISSN-L)
  • 1097-0215
OpenAlex
W1990059998
Cited by
132
References
28
Citations by year
2026: 1 · 2025: 2 · 2024: 1 · 2023: 6 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 3 · 2016: 4 · 2015: 3 · 2014: 7 · 2013: 2 · 2012: 4
FWCI
1.90
Type
journal article
Language
en
Open access
closed
Locations
  • International Journal of Cancer (publishedVersion)
  • PubMed (publishedVersion)
  • MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Digestive system and related health
Keywords
MUC2, colorectal adenoma, colorectal cancer, mucinous carcinoma, adenoma-carcinoma sequence, mucin expression, colonic mucosa, villous adenoma, tubular adenoma, mRNA expression
MeSH terms
Adenoma, Base Sequence, Adenocarcinoma, Mucinous, Diagnosis, Differential, Humans, Immunoenzyme Techniques, Molecular Sequence Data, Mucins, Neoplasm Proteins, Precancerous Conditions, RNA, Messenger, Biomarkers, Tumor, Colorectal Neoplasms, Gene Expression, Polymerase Chain Reaction, DNA Primers, Adenoma, Villous, Adenomatous Polyps, Mucin-2

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