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免疫组织化学检测到的结直肠癌中bcl-2表达:与肿瘤分期及患者生存率的相关性

Immunohistochemically detectable bcl-2 expression in colorectal carcinoma: correlation with tumour stage and patient survival.

作者信息

Ofner D, Riehemann K, Maier H, Riedmann B, Nehoda H, Tötsch M, Böcker W, Jasani B, Schmid K W

机构信息

Gerhard-Domagk-Institute of Pathology, University of Münster, Münster, Westfalia, Germany.

出版信息

Br J Cancer. 1995 Oct;72(4):981-5. doi: 10.1038/bjc.1995.446.

Abstract

The bcl-2 gene encodes for a mitochondrial membrane proto-oncoprotein, the expression of which is known to suppress programmed cell death (apoptosis). In the present study the prognostic value of bcl-2 proto-oncoprotein was immunohistochemically investigated in a series of 104 colorectal carcinomas. The bcl-2 staining patterns were semiquantitatively assessed and correlated with the pTNM stage, Dukes' classification, lymphocytic infiltration (Jass classification) and tumour grade as well as parameters not associated with prognosis (gender, age, tumour site, histological tumour type). Statistical analysis was carried out using the Kaplan-Meier method, the log-rank test, hazard ratios and their confidence intervals. Fifty-five out of 104 cases completely lacked immunohistochemical bcl-2 expression. Fewer than 5% of bcl-2-positive cells were found in 25, 5-50% in 17 and more than 50% in five cases. The extent of bcl-2 expression by tumour cells decreased significantly with respect to increasing tumour size (P < 0.05), decreasing lymphocytic infiltration (P < 0.05) and chance of poor clinical outcome (P < 0.05), but not with worsening of Dukes stages. In multivariate analysis (Cox regression model) bcl-2 expression remained as an independent prognostic parameter with Dukes' classification as stratification factor (P < 0.001). Although the biological functions of bcl-2 protein are not yet well understood, our results provide further evidence that bcl-2 oncoprotein appears to be associated with favourable clinical outcome. Thus immunohistochemical bcl-2 phenotyping of colorectal carcinoma may contribute in future to the clinical management of these patients.

摘要

bcl-2基因编码一种线粒体膜原癌蛋白,已知其表达可抑制程序性细胞死亡(凋亡)。在本研究中,采用免疫组织化学方法对104例结直肠癌患者的bcl-2原癌蛋白的预后价值进行了研究。对bcl-2染色模式进行半定量评估,并与pTNM分期、Dukes分期、淋巴细胞浸润(Jass分类)、肿瘤分级以及与预后无关的参数(性别、年龄、肿瘤部位、组织学肿瘤类型)进行相关性分析。采用Kaplan-Meier法、对数秩检验、风险比及其置信区间进行统计学分析。104例病例中有55例完全缺乏免疫组化bcl-2表达。25例中bcl-2阳性细胞少于5%,17例中为5%-50%,5例中超过50%。肿瘤细胞中bcl-2表达程度随肿瘤大小增加(P<0.05)、淋巴细胞浸润减少(P<0.05)和临床预后不良几率增加(P<0.05)而显著降低,但与Dukes分期恶化无关。在多因素分析(Cox回归模型)中,以Dukes分期为分层因素时,bcl-2表达仍是一个独立的预后参数(P<0.001)。尽管bcl-2蛋白的生物学功能尚未完全明确,但我们的结果进一步证明bcl-2癌蛋白似乎与良好的临床预后相关。因此,结直肠癌的免疫组化bcl-2表型分析未来可能有助于这些患者的临床管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c742/2034021/65904ccaf3d3/brjcancer00044-0183-a.jpg

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