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胃癌组织中Omi/HtrA2的表达及与预后的关系 被引量:6

Association of Omi/HtrA2 expression and prognosis in patients with gastric carcinoma
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摘要 目的 探讨丝氨酸蛋白酶Omi/HtrA2在胃癌组织中的表达及其与胃癌临床病理特征及预后的关系.方法 采用免疫组化法检测68例胃癌组织、15例癌旁组织及15例正常胃黏膜组织中Omi/HtrA2的表达,并分析其表达与胃癌临床病理特征及预后的关系.结果 Omi/HtrA2在胃癌组织中的阳性表达率为73.5%(50/68),高于癌旁组织(13.3%,2/15)和正常胃黏膜(6.7%,1/15),差异有统计学意义(P<0.05).胃癌组织中Omi/HtrA2的表达与患者的性别、年龄、肿瘤大小及浸润深度无关(P>0.05) 与肿瘤的分化程度、淋巴结转移和临床分期有关(P<0.05).本组胃癌患者5年总体生存率为63.3%,其中Omi/HtrA2表达阳性组和阴性组分别为72.0%和61.1%,两组比较,差异并无统计学意义(P>0.05).结论 Omi/HtrA2在胃癌组织中高表达,其表达与胃癌分化程度、淋巴结转移及TNM分期有关,但并不影响胃癌患者的预后. Objective To explore the expression of serine protease Omi/HtrA2 in gastric carcinoma tissue and its association with clinicopathological features and prognosis. Methods Omi/HtrA2 protein expression levels were detected by immunohistochemistry method in resected gastric carcinomas(n=68), adjacent noncancerous tissues(n=15), and normal tissues(n=15), and its association with clinicopathological features and prognosis were analyzed. Results Omi/HtrA2 expression was positive in 73.5%(50/68) of gastric cancer tissues, which was significantly higher than that in adjacent noncancerous tissues and normal tissues(P〈0.05). There were no significant differences in Omi/HtrA2 expression with respect to sex, age, tumor size, and depth of invasion(all P〉0.05). Omi/HtrA2 expression level was significantly associated with tumor differentiation, extent of lymph node metastasis, and tumor stage(all P〈0.05). Overall 5-year survival rate of patients with gastric carcinoma was 63.3%. Five-year survival rate was higher in Omi/HtrA2 positive cases than Omi/HtrA2 negative cases(72.0% vs. 61.1%), however the difference was not statistically significant. Conclusions Omi/HtrA2 expression is more common in gastric carcinoma. Omi/HtrA2 expression is associated with tumor differentiation, extent of lymph node metastasis, and tumor stage.
出处 《中华胃肠外科杂志》 CAS 北大核心 2010年第10期766-769,共4页 Chinese Journal of Gastrointestinal Surgery
基金 基金项目:广东省科技计划项目(20098030801144)
关键词 胃肿瘤 基因 OMI/HTRA2 细胞凋亡 预后 Stomach neoplasms Gene, Omi/HtrA2 Apoptosis Prognosis
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参考文献9

  • 1Srinivasula SM,Gupta S,Datta P,et al.Inhibitor of apoptosis proteins are substrates for the mitochondrial serine protease Omi/HtrA2.J Biol Chem,2003,278(34):31469-31472.
  • 2Verhagen AM,Silke J,Ekert PG,et al.HtrA2 promotes cell death through its serine protease activity and its ability to antagonize inhibitor of apoptosis proteins.J Biol Chem,2002,277(1):445-454.
  • 3Verhagen AM,Kratina TK,Hawkins CJ,et al.Identification of mammalian mitochondrial proteins that interact with IAPs via N-terminal IAP binding motifs.Cell Death Differ,2007,14(2):348-357.
  • 4Krick S,Shi S,Ju W,et al.Mpv17l protects against mitochondrial oxidative stress and apoptosis by activation of Omi/HtrA2 protease.Proc Natl Acad Sci USA,2008,105(37):14106-14111.
  • 5Hegde R,Srinivasula SM,Zhang Z,et al.Identification of Omi/HtrA2 as a mitochondrial apoptotic serine protease that disrupts inhibitor of apoptosis protein-caspase interaction.J Biol Chem,2002,277(1):432-438.
  • 6Martins LM,Iaccarino I,Tenev T,et al.The serine protease Omi/HtrA2 regulates apoptosis by binding XIAP through a reaper-like motif.J Biol Chem,2002,277(1):439-444.
  • 7Suzuki Y,Takahashi-Niki K,Akagi T,et al.Mitochondrial protease Omi/HtrA2 enhances caspase activation through multiple pathways.Cell Death Differ,2004,11(2):208-216.
  • 8Verhagen AM,Kratina TK,Hawkins CJ,et al.Identification of mammalian mitochondrial proteins that interact with IAPs via N-terminal IAP binding motifs.Cell Death Differ.,2007,14(2):348-357.
  • 9Liu Z,Li H,Derouet M,et al.Oncogenic Ras inhibits anoikis of intestinal epithelial cells by preventing the release of a mitochondrial pro-apoptotic protein Omi/HtrA2 into the cytoplasm.J Biol Chem,2006,281(21):14738-14747.

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