Nehls Oliver, Hass Holger G, Okech Thomas, Zenner Silke, Hsieh Chih-Jen, Sarbia Mario, Borchard Franz, Gruenagel Hans-Helmut, Gaco Vera, Porschen Rainer, Gregor Michael, Klump Bodo
Department of Internal Medicine I, University Hospital, 72076, Tübingen, Germany.
Int J Colorectal Dis. 2009 Jun;24(6):655-63. doi: 10.1007/s00384-009-0635-0. Epub 2009 Feb 17.
This study examined whether the apoptosis-related protein, BAX, or the microsatellite-instability phenotype provide prognostic information in patients with resected colon cancer.
A total of 371 stage I-III patients that previously underwent radical surgery were included (mean follow-up 51.8 months). BAX expression was examined by immunohistochemical staining; high-frequency microsatellite instability (MSI+) was determined by assessing the specific marker, BAT26, using single-strand conformation polymorphism (SSCP)-based analysis.
High BAX expression was found in 66.4% of patients. MSI+ tumors were observed in 14.8% of 344 patients. Univariate analysis showed that unlike MSI, low BAX expression was significantly correlated with poor disease-specific overall survival (OS) in stages I-III (p = 0.04). Multivariate subgroup analyses revealed that unlike MSI, low BAX was an independent predictor for OS in stage II (p = 0.009); however, in stages I or III, BAX or MSI were not independent predictors of OS.
In stage II colon cancer treated with surgery alone, BAX protein expression may be a predictor for prognosis.
本研究旨在探讨凋亡相关蛋白BAX或微卫星不稳定性表型是否能为接受结肠癌切除术的患者提供预后信息。
纳入371例先前接受根治性手术的I-III期患者(平均随访51.8个月)。通过免疫组织化学染色检测BAX表达;采用基于单链构象多态性(SSCP)分析的方法,通过评估特异性标志物BAT26来确定高频微卫星不稳定性(MSI+)。
66.4%的患者BAX表达较高。在344例患者中,14.8%观察到MSI+肿瘤。单因素分析显示,与MSI不同,低BAX表达与I-III期疾病特异性总生存期(OS)较差显著相关(p = 0.04)。多因素亚组分析显示,与MSI不同,低BAX是II期OS的独立预测因子(p = 0.009);然而,在I期或III期,BAX或MSI不是OS的独立预测因子。
在仅接受手术治疗的II期结肠癌中,BAX蛋白表达可能是预后的预测因子。