» Articles » PMID: 17708554

Diagnostic Value of Mucins (MUC1, MUC2 and MUC5AC) Expression Profile in Endoscopic Ultrasound-guided Fine-needle Aspiration Specimens of the Pancreas

Overview
Journal Int J Cancer
Specialty Oncology
Date 2007 Aug 22
PMID 17708554
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Mucins are aberrantly expressed in various malignancies. We immunohistochemically tested mucins expression (MUC1, MUC2 and MUC5AC) in EUS-FNA samples from pancreatic occupying lesions for the diagnostic utility. The prevalence of MUC1, MUC2 and MUC5AC expression in pancreatic cancers were 77.5% (31/40), 10.0% (4/40) and 80.0% (32/40), respectively, and in the benign pancreatic diseases 25% (4/16), 31.3% (5/16) and 43.8% (7/16). MUC1 and MUC5AC significantly overexpressed in pancreatic cancer, and MUC1 negatively related with tumor differentiation degree (p < 0.05). The prevalence of MUC1, MUC2 and MUC5AC expression in pancreatic mucinous neoplasms were 66.7% (12/18), 38.9% (7/18) and 88.9% (16/18), respectively, and in the pancreatic non-mucinous neoplasms 60.5% (23/38), 5.3% (2/38) and 57.9% (22/38). MUC2 and MUC5AC significantly overexpressed in pancreatic mucinous neoplasms, especially MUC2 in benign mucinous neoplasms (p < 0.05). Compared with cytology alone, the combination test of MUC1+cytology, and MUC5AC+cytology could achieve higher sensitivity (85 vs. 65%, 100 vs. 65%) and accuracy (89.3% vs. 73.2%, 91.1% vs. 73.2%) for pancreatic cancer diagnosis; the combination test of MUC2 + cytology, and MUC5AC + cytology could achieve higher sensitivity (77.8% vs. 38.9%, 100% vs. 38.9%), and specificity (97.4% vs. 60.5%, 71.1% vs. 60.5%) accuracy (100% vs. 51.8%, 80.4% vs. 51.8%) for mucinous neoplasm diagnosis. The panel MUC1+/MUC2-/MUC5AC+/ was higher specific in pancreatic cancer diagnosis, as well as MUC1-/MUC2+/MUC5AC+/ in pancreatic mucinous neoplasms. Our observations suggest the mucins expression profile in EUS-FNA specimens has higher value for the diagnosis of pancreatic cancer and mucinous neoplasms.

Citing Articles

The Past, Present, and Future of Biomarkers for the Early Diagnosis of Pancreatic Cancer.

Vitale F, Zileri Dal Verme L, Paratore M, Negri M, Nista E, Ainora M Biomedicines. 2025; 12(12.

PMID: 39767746 PMC: 11673965. DOI: 10.3390/biomedicines12122840.


Molecular Aberrations in Periampullary Carcinoma.

Tewari M, Swain J, Dixit V, Shukla H Indian J Surg Oncol. 2022; 8(3):348-356.

PMID: 36118392 PMC: 9478047. DOI: 10.1007/s13193-017-0645-2.


Mucin 5AC expression is common but unrelated to tumor progression in pancreatic adenocarcinoma.

Rico S, Buscheck F, Dum D, Luebke A, Kluth M, Hube-Magg C Int J Immunopathol Pharmacol. 2022; 36:3946320221106504.

PMID: 35764407 PMC: 9247369. DOI: 10.1177/03946320221106504.


Biomarkers in the diagnosis of pancreatic cancer: Are we closer to finding the golden ticket?.

ONeill R, Stoita A World J Gastroenterol. 2021; 27(26):4045-4087.

PMID: 34326612 PMC: 8311531. DOI: 10.3748/wjg.v27.i26.4045.


Quantitative assessment of the diagnostic role of mucin family members in pancreatic cancer: a meta-analysis.

Wang S, You L, Dai M, Zhao Y Ann Transl Med. 2021; 9(3):192.

PMID: 33708819 PMC: 7940915. DOI: 10.21037/atm-20-5606.