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ERCC1在胃癌中的表达及预后意义 被引量:7

Expression and prognostic significance of ERCC1 protein in gastric cancer
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摘要 目的:探讨核苷酸切除修复交叉互补组1(ERCC1)在胃癌中的表达水平及其对于生存的预后意义。方法:对85例完全切除的I~III期胃癌患者进行临床病理回顾性分析和随访,免疫组化分析采用PV-9000二步法。结果:(1)ERCC1蛋白在不同性别(P=0.364)、年龄(P=0.296)、PS评分(P=0.279)、病理组织分化程度(P=0.229)和TNM分期(P=0.154)患者中的表达均无差异。(2)ERCC1蛋白表达阴性组中位生存期(31个月)明显高于阳性组(23个月),差异具有统计学意义(P=0.048)。(3)ERCC1蛋白表达阴性患者中化疗组中位生存期(35个月)高于未化疗组(25个月),差异具有统计学意义(P=0.044)。(4)COX多因素分析显示ERCC1蛋白表达水平(P=0.041)、TNM分期(P=0.000)为胃癌术后患者生存期的独立影响因素。结论:ERCC1蛋白可预测胃癌术后患者对铂类为主辅助化疗的敏感性;ERCC1蛋白表达水平是胃癌术后患者独立的生存预后因素。 Objective:To investigate the value of excision repair cross complementing group 1(ERCC1) protein expression for judgment of prognosis in gastric cancer.Methods:Eighty-five patients with stageⅠ-Ⅲ gastric cancer who underwent complete surgical resection were included in the study.They were retrospectively reviewed with immunohistochemical study.Result:(1) No differences of ERCC1 protein were found among patients with different genders,ages,performance statues,degrees of differentiation and pathological TNM stages(P=0.364,0.296,0.279,0.229 and 0.154).(2)The survival curve of positive ERCC1 expression was significantly lower than that of negative expression,with median OS(overall survival) 23months and 31 months respectively(P=0.048).(3)Among the patients with negative ERCC1 protein expression,the survival curve of the non-chemotherapy group was significantly lower than that of chemotherapy group,with median OS 25 months and 35 months respectively(P=0.044).(4)COX multivariate regression analysis showed that the expression of ERCC1 protein(P=0.041) and pathological TNM stage(P=0.000) were independent prognostic factors of gastric cancer patients.Conclusion:ERCC1 may play an important role in predicting the sensitivity to platinum-based adjuvant chemotherapy,and it is also an independent prognostic factor of resectable gastric cancer patients.
出处 《交通医学》 2010年第4期375-377,380,共4页 Medical Journal of Communications
关键词 胃癌 核苷酸切除修复交叉互补组1 免疫组织化学法 gastric cancer prognosis excision repair cross complemting group1 immenohistochemical method
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