## Abstract Mucins are aberrantly expressed in various malignancies. We immunohistochemistrically tested mucins expression (MUC1, MUC2 and MUC5AC) in EUSβFNA samples from pancreatic occupying lesions for the diagnostic utility. The prevalence of MUC1, MUC2 and MUC5AC expression in pancreatic cancer
Prognostic value of serum MUC5AC mucin in patients with cholangiocarcinoma
β Scribed by Chanchai Boonla; Sopit Wongkham; John Kieran Sheehan; Chaisiri Wongkham; Vajarabhongsa Bhudhisawasdi; Nisana Tepsiri; Chawalit Pairojkul
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 83 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Abstract
BACKGROUND
The authors recently showed that MUC5AC mucin, which is expressed aberrantly in tumor tissue, is present in significant concentrations in serum from patients with cholangiocarcinoma. Subsequently, determination of serum MUC5AC had high sensitivity and specificity for cholangiocarcinoma. In this study, the possible association between serum MUC5AC mucin and the clinical findings of the patients and their prognostic value were explored.
METHODS
The expression of MUC5AC mucin in serum samples from 179 patients with histologically confirmed cholangiocarcinoma were determined using immunoblotting.
RESULTS
Detection of serum MUC5AC was associated with patients with blood group Type A, largerβsized tumors (> 5 cm), and advancedβstage disease. Patients who had positive serum MUC5AC status had a significantly poorer prognosis (median survival, 127 days; 95% confidence interval [95% CI], 107β180 days) compared with patients who had negative serum MUC5AC status (median survival, 329 days; 95% CI, 199β458 days; P < 0.001). Multivariate analysis with adjustment for all covariates showed that patients who had positive serum MUC5AC status had a 2.5βfold higher risk of death compared with patients who had negative serum MUC5AC status (P < 0.001).
CONCLUSIONS
Serum MUC5AC was associated with tumor burden. The determination of serum MUC5AC may be predictive of poor patient outcome and may be useful in selecting possible treatment options for patients with cholangiocarcinoma. Cancer 2003;98:1438β43. Β© 2003 American Cancer Society.
DOI 10.1002/cncr.11652
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