Jeon Yong-Tark, Kang Sokbom, Kang Dae-Hee, Yoo Keun-Young, Park In-Ae, Bang Yung-Jue, Kim Jae Weon, Park Noh-Hyun, Kang Soon-Beom, Lee Hyo-Pyo, Song Yong-Sang
Department of Obstetrics and Gynecology, College of Medicine, Seoul National University, Seoul, Korea.
Cancer Epidemiol Biomarkers Prev. 2004 Sep;13(9):1538-42.
Cyclooxygenase-2 (COX-2) has been known to be related with various types of carcinoma, but we have insufficient knowledge about the association between COX-2 and endometrial cancer. Many have reported a close relationship between p53 expression and a poor prognosis in endometrial cancer, but it is unclear whether p53 is an independent prognostic factor. To clarify these uncertainties, we examined the expressions of COX-2 and p53 in endometrial cancer tissues. The study was carried on 152 endometrial cancer patients who had operation at Seoul National University Hospital. Paraffin-embedded tissue blocks were sectioned and immunostained using monoclonal anti-COX-2 and anti-p53 antibodies. Twenty-seven (17.8%) specimens stained as COX-2 positive. COX-2 positivity was more frequently observed in postmenopausal patients than in premenopausal patients (8.8% versus 25.0%; P = 0.009). However, COX-2 positivity did not show a statistically significant association with any other clinicopathologic characteristic (parity, body mass index, histotype, International Federation of Gynecology and Obstetrics stage, grade, lymph node metastasis, deep myometrial invasion, or p53 overexpression). Thirty-one (20.4%) specimens showed p53 overexpression and this was significantly correlated with an advanced stage (P = 0.001), poor differentiation (P < 0.001), lymph node metastasis (P = 0.012), and deep myometrial invasion (P < 0.001). Multivariate Cox regression analysis showed that advanced stage was an independent prognostic factor of survival, but p53 overexpression was not. COX-2 may be associated with endometrial cancer carcinogenesis during the postmenopausal period but not with tumor aggressiveness and p53 overexpression. The p53 overexpression was found to be strongly associated with endometrial cancer aggressiveness.
环氧化酶-2(COX-2)已被证实与多种类型的癌症相关,但我们对COX-2与子宫内膜癌之间的关联了解不足。许多研究报告了p53表达与子宫内膜癌预后不良之间的密切关系,但p53是否为独立的预后因素尚不清楚。为了阐明这些不确定性,我们检测了子宫内膜癌组织中COX-2和p53的表达。该研究对152例在首尔国立大学医院接受手术的子宫内膜癌患者进行。将石蜡包埋的组织块切片,并用抗COX-2单克隆抗体和抗p53抗体进行免疫染色。27例(17.8%)标本COX-2染色呈阳性。绝经后患者中COX-2阳性的发生率高于绝经前患者(8.8%对25.0%;P = 0.009)。然而,COX-2阳性与任何其他临床病理特征(产次、体重指数、组织类型、国际妇产科联盟分期、分级、淋巴结转移、肌层深部浸润或p53过表达)均无统计学意义上的关联。31例(20.4%)标本显示p53过表达,且这与晚期(P = 0.001)、低分化(P < 0.001)、淋巴结转移(P = 0.012)及肌层深部浸润(P < 0.001)显著相关。多因素Cox回归分析显示,晚期是生存的独立预后因素,但p53过表达不是。COX-2可能与绝经后子宫内膜癌的发生有关,但与肿瘤侵袭性及p53过表达无关。发现p53过表达与子宫内膜癌的侵袭性密切相关。