Cho Dae Sung, Joo Hee Jae, Oh Dong Keun, Kang Ji Hun, Kim Young Soo, Lee Kyi Beom, Kim Se Joong
Department of Urology, Ajou University School of Medicine, San-5, Wonchon- dong, Yeongtong-gu, Suwon 443-721, Korea.
Yonsei Med J. 2005 Feb 28;46(1):133-40. doi: 10.3349/ymj.2005.46.1.133.
The aim of this study was to investigate the relationship of cyclooxygenase (COX)-2 and p53 expression with prognosis in patients with conventional renal cell carcinoma (RCC). Formalin-fixed, paraffin-embedded tissue sections of conventional RCC from 92 patients, who had undergone radical nephrectomy, were examined for COX-2 and p53 expression by immunohistochemistry and compared with clinicopathological variables. The COX-2 expression significantly correlated only with tumor size (p=0.049), whereas the p53 expression profoundly correlated with the TNM stage (p=0.024), M stage (p=0.001), and metastasis (synchronous or metachronous; p=0.004). The COX-2 overexpression did not significantly associate with p53 positivity (p=0.821). The survival rate of patients correlated with the p53 expression (p<0.0001) but not with the COX-2 expression (p=0.7506). Multivariate analyses indicated that tumor size, M stage, and p53 expression were independent prognostic factors for cancer-specific survival. The COX-2 expression was not an independent factor. These results show that the increased expression of p53 was associated with metastasis and a worse prognosis in conventional RCC, which suggests that p53 might have played an important role in the progression of conventional RCC. The increased expression of COX-2 was associated only with tumor size, but may not be an important prognostic factor in conventional RCC. No association was observed between COX-2 overexpression and p53 positivity in conventional RCC.
本研究旨在探讨环氧化酶(COX)-2和p53表达与传统肾细胞癌(RCC)患者预后的关系。对92例行根治性肾切除术的传统RCC患者的福尔马林固定、石蜡包埋组织切片进行免疫组织化学检测,以观察COX-2和p53的表达情况,并与临床病理变量进行比较。COX-2表达仅与肿瘤大小显著相关(p=0.049),而p53表达与TNM分期(p=0.024)、M分期(p=0.001)及转移情况(同时性或异时性;p=0.004)密切相关。COX-2过表达与p53阳性无显著相关性(p=0.821)。患者的生存率与p53表达相关(p<0.0001),但与COX-2表达无关(p=0.7506)。多因素分析表明,肿瘤大小、M分期和p53表达是癌症特异性生存的独立预后因素。COX-2表达不是独立因素。这些结果表明,p53表达增加与传统RCC的转移及预后较差相关,这提示p53可能在传统RCC的进展中起重要作用。COX-2表达增加仅与肿瘤大小相关,但可能不是传统RCC的重要预后因素。在传统RCC中,未观察到COX-2过表达与p53阳性之间存在关联。