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Increased cyclooxygenase-2 expression is correlated with suppressed antitumor immunity in cervical adenocarcinomas
T-H Chen1, K Fukuhara, M Mandai
1Department of Gynecology and Obstetrics, Faculty of Medicine, Kyoto University, Sakyo-ku, Kyoto, Japan.
Abstract:
Cyclooxygenase-2 (COX-2) inhibition suppressed the growth of various tumors. The augmentation of antitumor immunity by increasing cytotoxic lymphocytes may be an important mechanism for COX-2 inhibition. Among cervical cancers, adenocarcinomas present more aggressive behavior and overexpressed COX-2. The expression of COX-2 and the CD8+ lymphocyte infiltrations were evaluated in this study by immunohistochemistry. We studied COX-2 expression and CD8+ lymphocyte infiltration in 55 women with cervical adenocarcinomas. COX-2 expression and tumor stromal CD8+ lymphocytes were evaluated by semiquantified methods. Tumor intraepithelial lymphocytes were counted under microscopic field of x200. Correlations between these data and other clinicopathologic features were investigated. Thirty-seven out of 55 (67.3%) cervical adenocarcinomas significantly expressed COX-2. Patients who died within 5 years showed higher percentage of COX-2 expression than survivors (100% vs 58.1%, P < 0.05). Victims also showed lesser intraepithelial CD8+ lymphocyte counts than survived patients (3.4 vs 26.4, P < 0.05). COX-2 expression and tumor intraepithelial lymphocyte count were reversely correlated with each other (correlation index: -0.38, P < 0.01). Up-regulated COX-2 expression and lesser tumor intraepithelial CD8+ lymphocyte count are poor prognostic indicators for cervical adenocarcinoma patients. COX-2 may play an important role in the suppression of host antitumor immunity in cervical adenocarcinomas.
Insights
High cyclooxygenase-2 (COX-2) expression and low CD8+ lymphocyte counts indicate poor prognosis in cervical adenocarcinoma. COX-2 may suppress the immune system
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Cyclooxygenase-2 (COX-2) inhibition shows potential in suppressing tumor growth.
- Cervical adenocarcinomas exhibit aggressive behavior and COX-2 overexpression.
- Augmenting antitumor immunity via cytotoxic lymphocytes is a proposed mechanism for COX-2 inhibition.
Purpose of the Study:
- To evaluate the expression of COX-2 and CD8+ lymphocyte infiltration in cervical adenocarcinomas.
- To investigate the correlation between COX-2 expression, CD8+ lymphocyte infiltration, and clinicopathologic features.
- To determine the prognostic significance of COX-2 and CD8+ lymphocytes in cervical adenocarcinoma.
Main Methods:
- Immunohistochemistry was used to assess COX-2 expression and CD8+ lymphocyte infiltration in 55 cervical adenocarcinoma samples.
- COX-2 expression and tumor stromal CD8+ lymphocytes were evaluated using semiquantitative methods.
- Intraepithelial lymphocytes were counted microscopically, and correlations with clinicopathologic data were analyzed.
Main Results:
- 67.3% of cervical adenocarcinomas (37/55) showed significant COX-2 expression.
- Patients who died within 5 years had higher COX-2 expression (100%) compared to survivors (58.1%).
- Deceased patients exhibited lower intraepithelial CD8+ lymphocyte counts (3.4) than survivors (26.4).
- A significant inverse correlation was found between COX-2 expression and intraepithelial CD8+ lymphocyte counts (r=-0.38, P<0.01).
Conclusions:
- Up-regulated COX-2 expression and decreased intraepithelial CD8+ lymphocyte counts are associated with a poor prognosis in cervical adenocarcinoma.
- COX-2 may play a crucial role in suppressing host antitumor immunity in this cancer type.
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