Department of Colorectal Surgery of Changhai Hospital, Second Military Medical University, Shanghai, 200433, China.
Int J Colorectal Dis. 2012 Apr;27(4):429-35. doi: 10.1007/s00384-011-1346-x. Epub 2011 Nov 12.
There is a lack of study concerning expression of Topoisomerase IIα (Topo IIα) and long-term results in colorectal cancer patients. We aimed to investigate the relationship between expression of Topo IIα and clinicopathological parameters including overall survival in colorectal cancer.
Paraffin-fixed specimens from a large prospective cohort of colorectal cancer patients who had been followed up for 4 years were assayed immunohistochemically.
Of 490 colorectal cancer patients accessible for Topo IIα expression, expression of Topo IIα was scored as (-) in 4 (0.8%) patients, (+) in 41 (8.4%) patients, (++) in 396 (80.8%) patients, and (+++) in 49 (10.0%) patients. Overexpression of Topo IIα was found to be related with lower T stage (p = 0.042), lower N stage (p = 0.038), and a lower incidence of recurrence with nearly significance (p = 0.053). Kaplan-Meier analyses showed that overexpression of Topo IIα was related with prolonged overall survival (p = 0.022) and disease-free survival (p = 0.036). Multivariate analyses showed that elevated serum CEA (p < 0.001), elevated serum CA199 (p = 0.002), poor differentiation (p = 0.001), advanced Dukes stage (p < 0.001), and lower expression of Topo IIα (p = 0.017) were independent predictive factors for poor prognosis.
Topo IIα expression is a valuable prognostic indicator for colorectal cancer and would be useful in treatment selection for early colorectal cancer and malignant colorectal polyps resected under endoscopy, especially when it is used in combination with serum CEA, CA199, and differentiation.
关于拓扑异构酶 IIα(Topo IIα)的表达与结直肠癌患者长期预后之间的研究较少。本研究旨在探讨 Topo IIα在结直肠癌中的表达与包括总生存期在内的临床病理参数之间的关系。
对一个大型前瞻性结直肠癌患者队列的石蜡固定标本进行免疫组织化学检测,这些患者已随访 4 年。
在可用于检测 Topo IIα表达的 490 例结直肠癌患者中,Topo IIα的表达评分(-)为 4 例(0.8%),(+)为 41 例(8.4%),(++)为 396 例(80.8%),(+++)为 49 例(10.0%)。Topo IIα过表达与较低的 T 分期(p=0.042)、较低的 N 分期(p=0.038)和具有显著意义的复发率降低相关(p=0.053)。Kaplan-Meier 分析表明,Topo IIα过表达与总生存期(p=0.022)和无病生存期(p=0.036)延长相关。多变量分析表明,血清 CEA 升高(p<0.001)、血清 CA199 升高(p=0.002)、分化差(p=0.001)、Dukes 分期较晚(p<0.001)和 Topo IIα低表达(p=0.017)是预后不良的独立预测因素。
Topo IIα的表达是结直肠癌的一个有价值的预后指标,对于早期结直肠癌和内镜下切除的恶性结直肠息肉的治疗选择将是有用的,特别是在与血清 CEA、CA199 和分化相结合使用时。