首页> 美国卫生研究院文献>British Journal of Cancer >Immunohistochemically detectable bcl-2 expression in colorectal carcinoma: correlation with tumour stage and patient survival.
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Immunohistochemically detectable bcl-2 expression in colorectal carcinoma: correlation with tumour stage and patient survival.

机译:免疫组织化学检测到的bcl-2在结直肠癌中的表达:与肿瘤分期和患者生存率的相关性。

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摘要

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.
机译:bcl-2基因编码线粒体膜原癌蛋白,已知其表达可抑制程序性细胞死亡(细胞凋亡)。在本研究中,对bcl-2原癌蛋白的预后价值进行了免疫组织化学研究,以检测104例大肠癌。 bcl-2染色模式进行了半定量评估,并与pTNM分期,Dukes分类,淋巴细胞浸润(Jass分类)和肿瘤等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)相关。使用Kaplan-Meier方法,对数秩检验,危险比及其置信区间进行统计分析。 104例病例中有55例完全缺乏免疫组织化学bcl-2表达。在25例中发现少于5%的bcl-2阳性细胞,在17例中发现5-50%,五例中超过50%。肿瘤细胞的bcl-2表达程度相对于肿瘤大小增加(P <0.05),淋巴细胞浸润减少(P <0.05)和较差的临床结果发生率(P <0.05)显着降低,但杜克斯病恶化却没有阶段。在多变量分析(Cox回归模型)中,bcl-2表达仍作为独立的预后参数,以Dukes分类作为分层因子(P <0.001)。尽管尚不清楚bcl-2蛋白的生物学功能,但我们的结果提供了进一步的证据,表明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表型可能会在将来为这些患者的临床治疗做出贡献。

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