Suppr超能文献

p53、bax、Bcl-2和Bcl-xL免疫组化表达在非小细胞肺癌切除标本中的预后价值

Prognostic value of immunohistochemical expression of p53, bax, Bcl-2 and Bcl-xL in resected non-small-cell lung cancers.

作者信息

Groeger A M, Esposito V, De Luca A, Cassandro R, Tonini G, Ambrogi V, Baldi F, Goldfarb R, Mineo T C, Baldi A, Wolner E

机构信息

Department of Cardio-Thoracic Surgery, University of Vienna, Vienna, Austria.

出版信息

Histopathology. 2004 Jan;44(1):54-63. doi: 10.1111/j.1365-2559.2004.01750.x.

Abstract

AIMS

Some experimental evidence suggests that in lung cancer, development, progression and an increased proliferation rate can be linked to apoptosis-related factors. In this study we evaluated the possible role of p53 and Bcl-2 gene family members as prognostic factors for non-small-cell lung cancer.

METHODS AND RESULTS

We investigated the immunohistochemical expression of p53 and Bcl-2 gene family members (bax, Bcl-2 and Bcl-xL) in 94 non-small-cell lung cancer specimens to establish the role of these genes in lung cancer pathogenesis, and to evaluate their prognostic importance. The expression of Bcl-2 was correlated with a shorter patient survival time and with the nodal status of the neoplasm. We also found frequent over-expression of bax and Bcl-xL to be of no prognostic significance. Finally, we found no correlation between frequent detection of aberrant p53 protein and expression of either Bcl-2, bax or Bcl-xL or with patient survival time.

CONCLUSIONS

This study confirms a relevant role for apoptosis-regulatory proteins in the pathogenesis of lung cancer, and highlights the possible role of Bcl-2 as a prognostic factor for this tumour.

摘要

目的

一些实验证据表明,在肺癌中,其发生、发展及增殖率增加可能与凋亡相关因子有关。在本研究中,我们评估了p53和Bcl-2基因家族成员作为非小细胞肺癌预后因素的可能作用。

方法与结果

我们研究了94例非小细胞肺癌标本中p53和Bcl-2基因家族成员(bax、Bcl-2和Bcl-xL)的免疫组化表达,以确定这些基因在肺癌发病机制中的作用,并评估其预后重要性。Bcl-2的表达与患者较短的生存时间及肿瘤的淋巴结状态相关。我们还发现bax和Bcl-xL的频繁过表达无预后意义。最后,我们发现异常p53蛋白的频繁检测与Bcl-2、bax或Bcl-xL的表达以及患者生存时间之间均无相关性。

结论

本研究证实了凋亡调节蛋白在肺癌发病机制中的相关作用,并突出了Bcl-2作为该肿瘤预后因素的可能作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验