Cyclooxygenase-2 Expression in Intrahepatic Cholangiocarcinoma / 한국간담췌외과학회지
Korean Journal of Hepato-Biliary-Pancreatic Surgery
; : 102-107, 2003.
Article
in Ko
| WPRIM
| ID: wpr-150494
Responsible library:
WPRO
ABSTRACT
BACKGROUND/AIMS: Cyclooxygenase (COX)-2 levels are elevated in several types of human cancer tissues. COX-2 is not constitutively expressed by most normal tissues, but it is rapidly induced by certain inflammatory cytokines, tumor promoters, growth factors and oncogenes. Inflammation is important risk factor for intrahepatic cholangiocarcinoma. Therefore, this study was aimed to evaluate the role of COX-2 in intrahepatic cholangiocarcinoma development. METHODS: 18 intrahepatic cholangiocarcinoma patients was conducted in this study. COX-2 expression was investigated by immunohistochemical staining in resected liver specimen that involved 47 hyperplasia, 30 low-grade dysplasia, 38 high- grade dysplasia and 18 cancer. The relationship of clinicopathological factor and COX-2 expression of cancer was evaluated. RESULTS: COX-2 expression was not observed in normal bile duct epithelium. COX-2 expression in high-gade dysplasia was higher than in low-grade dysplasia. COX-2 expression in cancer was higher than in hyperplasia, low-grade and high grade dysplasia. There was no significant correlation between clinicopathological factors and COX-2 expression in cancer. CONCLUSION: These findings suggest that COX-2 may play a role in the early and late carcinogensis of intrahepatic cholangiocarcinoma.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Oncogenes
/
Bile Ducts
/
Carcinogens
/
Risk Factors
/
Cytokines
/
Prostaglandin-Endoperoxide Synthases
/
Cholangiocarcinoma
/
Intercellular Signaling Peptides and Proteins
/
Epithelium
/
Cyclooxygenase 2
Type of study:
Etiology_studies
/
Risk_factors_studies
Limits:
Humans
Language:
Ko
Journal:
Korean Journal of Hepato-Biliary-Pancreatic Surgery
Year:
2003
Type:
Article