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Bcl-2蛋白与可治愈性非小细胞肺癌患者的预后

Bcl-2 protein and prognosis in patients with potentially curable non-small-cell lung cancer.

作者信息

Silvestrini R, Costa A, Lequaglie C, Mochen C, Veneroni S, Leutner M, Ravasi G

机构信息

Oncologia Sperimentale C, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.

出版信息

Virchows Arch. 1998 May;432(5):441-4. doi: 10.1007/s004280050188.

Abstract

The bcl-2 proto-oncogene functions as a cell death suppressor, and its expression prolongs cell survival by blocking apoptosis. Data available on the clinical relevance of bcl-2 protein expression in patients with non-small-cell lung cancer (NSCLC) are controversial. We analysed the role of bcl-2 protein expression on 6-year relapse-free survival in 229 patients with stage I-IIIa NSCLC (101 squamous cell carcinomas and 128 adenocarcinomas) subjected to surgery, with curative intent. Immunohistochemical analysis was performed on archival material by using a monoclonal antibody anti-bcl-2 (clone 124). Bcl-2 protein expression, which was detected in 22% of the cases, was significantly related to stage, histology and grading, and was an indicator of clinical outcome. The probability of relapse-free survival at 6 years was longer for patients with bcl-2-positive tumours (74%) than for those with bcl-2-negative tumours (57%) (P=0.02). This finding was mainly evident for the subgroups of patients with stage IIIa tumours (P=0.05), squamous cell carcinoma (P=0.03) or moderately/poorly differentiated tumours (P=0.02). However, multivariate analysis by Weibull's regression model indicated that bcl-2 protein expression was not an independent prognostic risk factor in patients with curable NSCLC when the information provided by stage was available.

摘要

bcl-2原癌基因起着细胞死亡抑制因子的作用,其表达通过阻断细胞凋亡来延长细胞存活时间。关于非小细胞肺癌(NSCLC)患者中bcl-2蛋白表达的临床相关性的现有数据存在争议。我们分析了bcl-2蛋白表达对229例I-IIIa期NSCLC(101例鳞状细胞癌和128例腺癌)行根治性手术患者6年无复发生存率的作用。使用抗bcl-2单克隆抗体(克隆124)对存档材料进行免疫组织化学分析。在22%的病例中检测到bcl-2蛋白表达,其与分期、组织学和分级显著相关,并且是临床结果的一个指标。bcl-2阳性肿瘤患者6年无复发生存的概率(74%)高于bcl-2阴性肿瘤患者(57%)(P=0.02)。这一发现主要在IIIa期肿瘤患者亚组(P=0.05)、鳞状细胞癌患者亚组(P=0.03)或中/低分化肿瘤患者亚组(P=0.02)中明显。然而,通过威布尔回归模型进行的多变量分析表明,当有分期提供的信息时,bcl-2蛋白表达在可治愈的NSCLC患者中不是一个独立的预后风险因素。

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