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Bcl-xL/Bcl-2相关死亡促进因子的下调表明小细胞肺癌患者的预后较差。

The downregulation of Bcl-xL/Bcl-2-associated death promoter indicates worse outcomes in patients with small cell lung carcinoma.

作者信息

Yu Yaoyang, Zhong Zhaokui, Guan Yaowu

机构信息

Department of Thoracic Surgery, Zhumadian Central Hospital Zhumadian 463000, Henan, China.

出版信息

Int J Clin Exp Pathol. 2015 Oct 1;8(10):13075-82. eCollection 2015.

Abstract

It is well known that lung cancer is the 1st leading cause of death worldwide. Many reports have demonstrated that Bad, the Bcl-xL/Bcl-2-associated death promoter plays a crucial role in the intrinsic apoptosis pathway. The aim of this study was to explore the expression of Bad and its clinical significance in small cell lung carcinoma (SCLC) By analyzing the expression of Bad in 147 SCLC patient specimen, we found that Bad expression was remarkably decreased in 55.8% (82/147) cases, compared with the neighboring non-tumor tissues. Further study showed that Bad expression was correlated with adverse clinical characters such as clinical stage (P = 0.001), tumor size (P = 0.036) and tumor recurrence (P = 0.030). Furthermore, the results of Kaplan-Meier analysis showed that low Bad expression was significantly correlated to overall survival (P < 0.0001) and disease-free survival (P = 0.017) of patients with SCLC. Moreover, multivariate analyses revealed that Bad was an independent indicator of overall survival in SCLC (hazard ration = 0.620, 95% confidence interval: 0.389-0.987, P < 0.001). In summary, we can conclude that patients with SCLC represent downregulation of Bad and the latter could be served as a useful biomarker for the outcomes of SCLC.

摘要

众所周知,肺癌是全球首要死因。许多报告表明,Bad,即Bcl-xL/Bcl-2相关死亡促进因子,在细胞内凋亡途径中起关键作用。本研究旨在探讨Bad在小细胞肺癌(SCLC)中的表达及其临床意义。通过分析147例SCLC患者标本中Bad的表达,我们发现与邻近非肿瘤组织相比,55.8%(82/147)的病例中Bad表达显著降低。进一步研究表明,Bad表达与临床分期(P = 0.001)、肿瘤大小(P = 0.036)和肿瘤复发(P = 0.030)等不良临床特征相关。此外,Kaplan-Meier分析结果显示,低Bad表达与SCLC患者的总生存期(P < 0.0001)和无病生存期(P = 0.017)显著相关。而且,多因素分析显示Bad是SCLC总生存期的独立指标(风险比 = 0.620,95%置信区间:0.389 - 0.987,P < 0.001)。总之,我们可以得出结论,SCLC患者存在Bad表达下调,后者可作为SCLC预后的有用生物标志物。

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