Abstract | AIMS: To compare the lineage specific distribution of MUC1 and MUC2 mucins in normal colorectal mucosa and adenocarcinoma and to identify pathological correlations. METHODS: RESULTS: MUC1, Lex and Ley co-localised with columnar cell secretions, whereas MUC2, mild periodic acid Schiff and sialosyl-Tn co-localised with goblet cell mucin in both normal and malignant tissues. Sialosyl-Lex and Tn were associated with both lineages. In normal tissues MUC1, Lex and Ley showed only trace expression by crypt base columnar cells. Cancers could be classified into four phenotypes (MUC2+/MUC1-, MUC2+/MUC1+, MUC2-/MUC1+, MUC2-/MUC1-). Particular phenotypes showed significant correlations with cancer type, lymph node spread and peritumoral lymphocytic infiltration and trends falling short of significance in relation to grade of differentiation and contiguous adenoma. CONCLUSIONS: Classification of colorectal cancer by means of lineage specific function may be relevant to both pathogenesis and prognosis.
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Authors | Y Ajioka, L J Allison, J R Jass |
Journal | Journal of clinical pathology
(J Clin Pathol)
Vol. 49
Issue 7
Pg. 560-4
(Jul 1996)
ISSN: 0021-9746 [Print] England |
PMID | 8813954
(Publication Type: Journal Article)
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Chemical References |
- Biomarkers, Tumor
- Epitopes
- MUC2 protein, human
- Mucin-1
- Mucin-2
- Mucins
- Neoplasm Proteins
- Sialic Acids
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Topics |
- Adenocarcinoma
(chemistry, pathology)
- Aged
- Biomarkers, Tumor
(analysis)
- Colorectal Neoplasms
(chemistry, pathology)
- Epitopes
(analysis)
- Female
- Humans
- Immunohistochemistry
- Intestinal Mucosa
(chemistry, pathology)
- Male
- Mucin-1
(analysis)
- Mucin-2
- Mucins
(analysis)
- Neoplasm Proteins
(analysis)
- Sialic Acids
(analysis)
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