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Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2.

Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Research Abstract Details 

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  • Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Abstract Text:

    j h b van de bovenkampJ H B Van De Bovenkamp,a m korteland-van maleA M Korteland-Van Male,c warsonC Warson,h a H A ,a w c einerhandA W C Einerhand,n l e y ectorsN L E Y Ectors,j dekkerJ Dekker,

    AIMS: Barrett's oesophagus constitutes metaplastic epithelium, often diagnosed by mucin histochemistry. We determined the mucins and trefoil factor family (TFF)-peptides that were expressed in Barrett's oesophagus, in order to study changes in protein expression in early stages of Barrett's oesophagus development. METHODS AND RESULTS: Biopsy specimens of 71 Barrett's oesophagus patients were collected, and sections were stained for secretory mucins by histochemistry. Immunohistochemistry was performed for secretory mucins (MUC2, MUC5AC, MUC5B, MUC6), TFFs (TFF1, TFF2, TFF3), and proliferation (Ki67). Protein expression in the tissue was measured semiquantitatively. MUC5AC and TFF1 showed high levels and strong colocalization in the surface epithelium, whereas MUC6, MUC5B and TFF3 were found in the deeper glandular structures. TFF2 was found in both surface and glandular epithelium. The co-ordinate expression patterns of these six markers were similar to gastric antrum epithelium. MUC2 expression was ubiquitously associated with goblet cells within intestinal metaplasia, occurring in 68% of patients, and was correlated with increasing proliferation in the epithelium. CONCLUSIONS: Virtually all cells in Barrett's oesophagus epithelium displayed a secretory phenotype, demonstrating a co-ordinate gastric-type MUC and TFF expression. When MUC2 expression was more pronounced, the expression patterns of the other MUCs and the TFFs were increasingly disturbed. MUC2 expression may constitute a marker for early change in the phenotype of Barrett's oesophagus as a precancerous lesion.

    Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Publishing Authors By Initials

    jh van de bovenkampJH Van De Bovenkamp,am korteland-van maleAM Korteland-Van Male,c warsonC Warson,ha HA ,aw einerhandAW Einerhand,nl ectorsNL Ectors,j dekkerJ Dekker,

    For similar biological factors: biological markers: tumor markers, biological research abstracts see: biological factors: biological markers: tumor markers, biological research

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    Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Histopathology

    VOLUME: 42

    Page Numbers: 555-65

    Journal Abbreviation: Histopathology

    ISSN: 0309-0167

    DAY: 30

    MONTH: Jun

    YEAR: 2003

    Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7704136

    Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Keywords Mesh Terms:

    KEYWORDS: Tumor Markers, Biological

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2. Information

    Substance Name: trefoil factor

    Registry Number: 146046-78-8

    Grant and Affiliation Information for Gastric-type mucin and TFF-peptide expression in Barrett's oesophagus is disturbed during increased expression of MUC2.

    AFFILIATION: Laboratory of Paediatrics and Sophia Children's Hospital, Erasmus MC, Rotterdam, the Netherlands.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Histopathology

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