非小细胞肺癌XIAP和Smac的表达与临床病理特征及预后的关系

Expression of XIAP and Smac in human non-small-cell lung carcinoma(NSCLC)and the relationship with clinical significance and prognosis

  • 摘要:
      目的   探讨XIAP(X-linked inhibitor of apoptosis protein,XIAP)和Smac(second mitochondria-derived activator of caspase,Smac)在非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中的表达与临床病理特征及预后的关系。
      方法   采用免疫组织化学法检测70例非小细胞肺癌组织及70例对应癌旁肺组织中XIAP、Smac的表达。
      结果   XIAP在70例NSCLC组织中有59例阳性表达,其中高表达16例;对应70例癌旁肺组织中有52例表达,其中高表达5例,两组XIAP表达强度比较差异有统计学意义(Z=-4.049,P < 0.001);Smac在70例肺癌组织中有63例阳性表达,其中高(强阳性)表达32例;对应70例癌旁肺组织有53例表达,其中高(强阳性)表达5例,两组Smac表达强度比较差异有统计学意义(Z=-5.484,P < 0.001)。NSCLC组织中XIAP、Smac的表达与患者的性别、年龄、肿瘤大小、组织类型、分化程度、吸烟与否等无明显关系(P <0.05);但二者的表达均与临床分期、淋巴结转移与否有关系(P < 0.05)。通过Kaplan-Meier法分析得出,XIAP和Smac在NSCLC中的表达与患者的预后均无明显关系(P <0.05)。
      结论   1)XIAP和Smac在非小细胞肺癌组织及其对应癌旁肺组织中均有表达,但存在表达量的差异。2)XIAP和Smac在非小细胞肺癌中的表达与患者的预后均无显著关系。

     

    Abstract:
      Objective   To investigate the expression of XIAP and Smac in human non-small-cell lung carcinoma (NSCLC) and the relationship with clinical significance and prognosis.
      Methods   Immunohistochemical staining was performed to determine the expression of X-linked inhibitor of apoptosis protein (XIAP) and second mitochondria-derived activator of caspase (Smac) in 70 cases of NSCLC and 70 cases of non-cancerous adjacent lung tissues.
      Results   XIAP is mostly present (59/70) in tumor tissues with 16 high expressions, whereas only five high expressions in non-cancerous adjacent lung tissues are observed (52/70). The statistical difference of these two sets of data is significant (Z=-5.484, P < 0.001). Comparatively, Smac is present (63/70) in tumor tissues, which is significantly (Z=-5.484, P < 0.001) higher than in the non-cancerous adjacent lung tissues (53/70). The expression levels of XIAP and Smac in NSCLC tissues are closely related to the lymph node metastasis at the TNM stages (P < 0.05) and not associated to gender, age, size of tumor, and differentiation grades (P <0.05). The Kaplan-Meier analysis results show that survival by XIAP and Smac protein in NSCLC has no significant effect (P <0.05).
      Conclusion   XIAP and Smac are expressed in NSCLC and noncancerous adjacent lung tissues, and the differences in their expression levels is significant. The deterioration of NSCLC results in apoptosis/anti-apoptotic synchronized with tumor cell proliferation. The expression levels of XIAP and Smac in NSCLC are not related with the prognosis.

     

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