Prognostic significance of cyclooxygenase-2 and DNA topoisomerase IIα expression in oral carcinoma
✍ Scribed by Kazunari Sakurai; Masahiro Urade; Kazuma Noguchi; Susumu Hashitani; Kazuki Takaoka; Emi Segawa; Hiromitsu Kishimoto
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 240 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background.
Despite recent advances in the diagnosis and treatment of oral carcinoma, outcomes remain disappointing. The identification of new prognostic factors is necessary to improve survival. To determine the prognostic significance of cyclooxygenase (COX)‐2 and DNA topoisomerase (DNA‐Topo) IIα expression in patients with oral carcinoma, we immunohistochemically examined these enzymes and studied their relation to overall 5‐year survival.
Methods.
Surgical specimens were obtained from 160 patients with oral carcinoma, 80 with and 80 without regional lymph node metastasis. The specimens were immunostained for COX‐2 and DNA‐Topo IIα as an index of cell proliferative activity. COX‐2 immunoreactivity and clinicopathological data were analyzed, and 5‐year survival was calculated by the Kaplan‐Meier method.
Results.
COX‐2 expression in primary lesions was higher in cases with lymph node metastasis than in those without lymph node metastasis. An increase in tumor size was associated with increased COX‐2 expression. In most cases with lymph node metastasis, COX‐2 expression was higher in metastatic lesions than in primary lesions. As COX‐2 expression increased, the DNA‐Topo IIα labeling index significantly increased and the overall 5‐year survival rate decreased.
Conclusion.
Expression of COX‐2 and DNA‐Topo IIα were related to lymph node metastasis, cell proliferative activity, and overall 5‐year survival rate in oral carcinoma. These enzymes may therefore be valuable diagnostic and prognostic indices in oral carcinoma. © 2007 Wiley Periodicals, Inc. Head Neck, 2007
📜 SIMILAR VOLUMES
## Abstract ## Background Cyclooxygenase (COX)‐2 is believed to be an important enzyme related to the pathogenesis of colorectal cancer (CRC). p53 has been reported to be a negative regulator of COX‐2 expression in in vitro studies. The aim of this study was to investigate COX‐2 expression and its