Fernández R, Vizoso F, Rodríguez J C, Merino A M, González L O, Quintela I, Andicoechea A, Truan N, Díez M C
Servicio de Cirugía General y Anatomía Patológica, Hospital de Jove, Gijón, Spain.
Ann Surg Oncol. 2000 Aug;7(7):508-14. doi: 10.1007/s10434-000-0508-9.
In this study we evaluated the expression and clinical significance of pepsinogen C, an aspartic proteinase involved in the digestion of proteins in the stomach, in patients with gastric cancer.
Pepsinogen C expression was examined by immunohistochemical methods in a series of 95 gastric carcinomas. The prognostic value of pepsinogen C was retrospectively evaluated by multivariate analysis taking into account conventional prognostic parameters. Follow-up period of patients was 21.4 months.
A total of 25 (26.3%) gastric carcinomas stained positively for pepsinogen C. The percentage of pepsinogen C-positive tumors was higher in well-differentiated (50%) than in moderately differentiated (19.5%) and poorly differentiated (21.9%) tumors (P < .05). Similarly, significant differences in pepsinogen C immunostaining were found between node-negative and node-positive tumors (47.1% vs. 14.7%; P < .001). In addition, statistical analysis revealed that pepsinogen C expression was associated with clinical outcome in gastric cancer patients. Low pepsinogen C levels predicted short overall survival periods in the overall group of patients with gastric cancer (P < .001), and in 71 patients with resectable carcinomas (P < .005). Multivariate analysis according to Cox's model indicated that pepsinogen C immunostaining was an independent predictor of outcome for both overall and resectable gastric cancer patients (P < .05, for both).
The expression of pepsinogen C in gastric cancer may represent a useful biological marker able to identify subgroups of patients with different clinical outcomes.
在本研究中,我们评估了参与胃内蛋白质消化的天冬氨酸蛋白酶胃蛋白酶原C在胃癌患者中的表达及临床意义。
采用免疫组化方法检测了95例胃癌组织中胃蛋白酶原C的表达。考虑到传统的预后参数,通过多因素分析对胃蛋白酶原C的预后价值进行了回顾性评估。患者的随访期为21.4个月。
共有25例(26.3%)胃癌组织胃蛋白酶原C染色呈阳性。高分化肿瘤(50%)中胃蛋白酶原C阳性肿瘤的比例高于中分化(19.5%)和低分化(21.9%)肿瘤(P<0.05)。同样,在无淋巴结转移和有淋巴结转移的肿瘤之间,胃蛋白酶原C免疫染色存在显著差异(47.1%对14.7%;P<0.001)。此外,统计分析显示胃蛋白酶原C的表达与胃癌患者的临床结局相关。低胃蛋白酶原C水平预示着胃癌患者总体生存期较短(P<0.001),在71例可切除癌患者中也是如此(P<0.005)。根据Cox模型进行的多因素分析表明,胃蛋白酶原C免疫染色是总体胃癌患者和可切除胃癌患者预后的独立预测因子(两者均P<0.05)。
胃蛋白酶原C在胃癌中的表达可能是一种有用的生物学标志物,能够识别具有不同临床结局的患者亚组。