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