Trypsinogen-1,-2 and tumour-associated trypsin-inhibitor in bile and biliary tract tissues from patients with biliary tract diseases and pancreatic carcinomas

Citation
J. Hedstrom et al., Trypsinogen-1,-2 and tumour-associated trypsin-inhibitor in bile and biliary tract tissues from patients with biliary tract diseases and pancreatic carcinomas, SC J CL INV, 61(2), 2001, pp. 111-118
Citations number
33
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
Journal title
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
ISSN journal
00365513 → ACNP
Volume
61
Issue
2
Year of publication
2001
Pages
111 - 118
Database
ISI
SICI code
0036-5513(200104)61:2<111:TATTIB>2.0.ZU;2-8
Abstract
The bile concentrations of trypsinogen-1, -2 and tumour-associated trypsin- inhibitor (TATI) were determined in 23 patients with benign biliary tract d isease, two with biliary tract cancer, and in 15 with pancreatic cancer. We also examined the trypsinogen and TATI expression by immunohistochemistry in tissue specimens from biliary tract cancer and non-neoplastic extrahepat ic biliary tract. High levels of trypsinogen-1, trypsinogen-2, and TATI occ ur in bile of most patients. In contrast to the trypsinogens, the levels of TATI were significantly higher in patients with malignant disease than in those with benign diseases (p=0.04). There was no significant correlation b etween trypsinogen-2 and amylase (r = 0.13, p = 0.40), indicating that the occurrence of trypsinogen in bile is not a result of reflux of pancreatic f luid into the bile duct. Immunohistochemically, trypsinogen-2 was detected in five and TATI in 12 out of 15 non-neoplastic biliary tract specimens, an d in four and seven out of 11 cholangiocarcinomas, respectively. High conce ntrations of trypsinogen-l, trypsinogen-2 and TATI occur in the bile of pat ients with non-neoplastic and malignant biliary tract disease and in patien ts with pancreatic cancer. At least part of the trypsinogen-2 and TATI foun d in bile appears to be derived from the biliary epithelium itself.