Premium
Role of cyclooxygenase‐2 in immunomodulation and prognosis of endometrial carcinoma
Author(s) -
Ohno Yumiko,
Ohno Satoshi,
Suzuki Nobutaka,
Kamei Tsutomu,
Inagawa Hiroyuki,
Soma GenIchiro,
Inoue Masaki
Publication year - 2005
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.20777
Subject(s) - endometrial cancer , proportional hazards model , cd8 , immune system , carcinoma , medicine , oncology , hazard ratio , univariate analysis , cancer research , cancer , immunology , multivariate analysis , confidence interval
Although there are several hypotheses explaining the mechanisms of immune‐privileged status of malignant tumor, the exact pathway has yet to be explored. Cyclooxygenase (COX)‐2 plays a vital role in prognosis of cancer patients in terms of contribution to neoangiogenesis and apoptosis inhibition; however, the impact of COX‐2 in immunomodulation has not been reported. We have evaluated the expression of COX‐2 and its impact on infiltration of immune‐competent cells into the tumor cell nest in endometrial carcinoma. Tissue specimens from 70 endometrial carcinoma patients who had undergone a curative resection were evaluated for COX‐2 expression and host immune status (CD8 + T cells). COX‐2 expression was associated with FIGO stage and myometrial invasion, but there was no statistically significant impact. CD8 + T cells within cancer cell nest (Nest CD8) were inversely correlated with the expression level of COX‐2 ( p = 0.0006). Nest CD8 became an independent predictor of patient survival (Hazard ratio = 10.300, p = 0.0304) in Cox's multivariate analysis. The expression level of COX‐2 was found to be a significant predictor of disease relapse in univariate analysis ( p = 0.0294) but not in multivariate analysis ( p = 0.5949). In conclusion, increased nest CD8 produced a survival advantage in endometrial carcinoma patients. Moreover, tumor‐produced COX‐2, which reduces the infiltration of CD8 + T cells into cancer cell nests, may allow tumors to avoid immune surveillance. © 2004 Wiley‐Liss, Inc.