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p53表达在胃癌中的预后影响。

Prognostic influence of p53 expression in gastric cancer.

作者信息

Müller W, Borchard F

机构信息

Department of Pathology, Heinrich-Heine University of Düsseldorf, Germany.

出版信息

J Pathol. 1996 Mar;178(3):255-8. doi: 10.1002/(SICI)1096-9896(199603)178:3<255::AID-PATH468>3.0.CO;2-V.

Abstract

The presence of the nuclear phosphoprotein p53 was investigated in a series of 120 consecutive gastric carcinomas. This immunohistochemical study on formalin-fixed, paraffin-embedded material found p53 expression in 43 per cent (n = 51) of carcinomas using a monoclonal antibody (DO-1), whereas no immunoreactivity for p53 was present in tumour-associated non-neoplastic gastric mucosa or tumour stroma. There was no statistically significant correlation with known prognostic parameters such as extent of tumour growth (pT state), nodal involvement (pN state), or tumour grade. The same applied for association with patient age and sex or pathological parameters such as tumour size, localization, or growth pattern according to histological classification. Kaplan-Meier analysis revealed marginal statistically significant differences in survival times between patients with p53-positive tumours with more than 35 per cent of p53-positive tumour cells and those with less than 35 per cent of p53-positive tumour cells or p53-negative tumours (P = 0.04). However, by multivariate analysis, p53 immunoreactivity did not turn out as an independent prognostic parameter. p53 expression can easily be detected in a variety of human malignancies including gastric cancer by immunohistochemical methods, but its prognostic significance and possible role as an independent marker of poor prognosis still have to be confirmed by further studies.

摘要

对连续的120例胃癌进行了核磷蛋白p53表达情况的研究。这项针对福尔马林固定、石蜡包埋材料的免疫组织化学研究发现,使用单克隆抗体(DO-1)时,43%(n = 51)的癌组织中有p53表达,而在肿瘤相关的非肿瘤性胃黏膜或肿瘤间质中未检测到p53免疫反应性。p53表达与肿瘤生长范围(pT分期)、淋巴结受累情况(pN分期)或肿瘤分级等已知预后参数之间无统计学显著相关性。对于与患者年龄、性别或病理参数(如肿瘤大小、位置或根据组织学分类的生长模式)的相关性,情况也是如此。Kaplan-Meier分析显示,p53阳性肿瘤细胞超过35%的患者与p53阳性肿瘤细胞少于35%或p53阴性肿瘤的患者相比,生存时间存在边缘性统计学显著差异(P = 0.04)。然而,通过多变量分析,p53免疫反应性并未成为独立的预后参数。通过免疫组织化学方法可以很容易地在包括胃癌在内的多种人类恶性肿瘤中检测到p53表达,但其预后意义以及作为预后不良独立标志物的可能作用仍有待进一步研究证实。

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