S-Space College of Medicine/School of Medicine (의과대학/대학원) Dermatology (피부과학전공) Journal Papers (저널논문_피부과학전공)
Cyclooxygenase-2 and inducible nitric oxide synthase expression in thyroid neoplasms and their clinicopathological correlation
- Kim, Kyung-Hee; Kim, Seong-Ho; Kim, Seok Hyung; Back, Jong-Ho; Park, Mee-Ja; Kim, Jin-Man
- Issue Date
- Korean Academy of Medical Science
- J Korean Med Sci. 2006 Dec;21(6):1064-9.
- Adult; Aged; Cyclooxygenase 2/*analysis; Female; Gene Expression Profiling; Humans; Male; Middle Aged; Neoplasm Proteins/*analysis; Nitric Oxide Synthase Type II/*analysis; Reproducibility of Results; Sensitivity and Specificity; Statistics as Topic; Thyroid Neoplasms/*diagnosis/*enzymology; Tissue Distribution; Tumor Markers, Biological/*analysis
- To evaluate the expressions of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in thyroid neoplasms in a Korean population, we studied a total of 154 cases: papillary carcinoma of classical type (PTC), 86; follicular adenoma (FA), 21; follicular carcinoma (FC), 35; medullary carcinoma (MC), 3; undifferentiated carcinoma (UC), 5; and Hurthle cell neoplasm (HN), 4. Using immunohistochemical staining, COX-2 expression was detected in 62 (72.1%) PTC specimens, 5 (23.8%) FA specimens, 10 (28.6%) FC specimens, 0 (0.0%) MC specimens, 1 (20.0%) UC specimen, and 3 (75%) HN specimens. iNOS expression was detected in 66 (76.7%) PTC specimens, 4 (19.0%) FA specimens, 13 (37.1%) FC specimens, 0 (0.0%) MC specimens, 3 (60.0%) UC specimens, and 4 (100%) HN specimens. The results showed that COX-2 and iNOS were frequently expressed in the PTC and HN specimens, and iNOS was more frequently overexpressed in the FC specimens than in the FA specimens. In PTC, COX-2 and iNOS were significantly overexpressed in patients over 45 yr of age (p=0.029, p=0.041), and iNOS expression was increased in patients with a large primary tumor (p=0.028). These results suggest that the upregulation of COX-2 and iNOS may contribute to the tumor progression of thyroid gland, particularly in PTC and HN, and iNOS may play an adjuvant role during the tumor progression of FC.
- 1011-8934 (Print)