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细胞周期调节蛋白细胞周期蛋白D1、细胞周期蛋白E及其抑制剂p21 WAF1/CIP1在胃癌中的表达

Expression of cell-cycle regulatory proteins cyclin D1, cyclin E, and their inhibitor p21 WAF1/CIP1 in gastric cancer.

作者信息

Müller W, Noguchi T, Wirtz H C, Hommel G, Gabbert H E

机构信息

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

出版信息

J Pathol. 1999 Oct;189(2):186-93. doi: 10.1002/(SICI)1096-9896(199910)189:2<186::AID-PATH418>3.0.CO;2-L.

Abstract

The expression and prognostic role of cyclin D1, cyclin E, and p21 (WAF1/CIP1) were immunohistochemically investigated in 413 curatively resected gastric carcinomas. p21 was expressed in 65.4 per cent (n=270), cyclin D1 in 23.7 per cent (n=98), and cyclin E in 13.6 per cent ( n=56) of the tumours. The expression of p21, cyclin D1, and cyclin E was positively associated with the papillary or tubular type of the WHO classification, as well as with the intestinal type according to the Lauren classification. No significant correlation could be found between the expression of p21, cyclin D1 and cyclin E and the parameters pT category, lymph node involvement, and blood vessel and lymphatic vessel invasion. Concerning survival, no prognostic impact of p21, cyclin D1, and cyclin E expression could be verified, even when different subgroups of patients were analysed separately according to the pT and pN category as well as to the Lauren classification. The present data suggest that neither cyclin D1, cyclin E nor their inhibitor p21 can predict the survival of gastric cancer patients, nor is their immunohistochemical detection a suitable tool for identifying subgroups of patients who may be at higher risk.

摘要

我们采用免疫组织化学方法研究了413例接受根治性切除的胃癌组织中细胞周期蛋白D1、细胞周期蛋白E和p21(WAF1/CIP1)的表达情况及其预后作用。结果显示,p21在65.4%(n=270)的肿瘤组织中表达,细胞周期蛋白D1在23.7%(n=98)的肿瘤组织中表达,细胞周期蛋白E在13.6%(n=56)的肿瘤组织中表达。p21、细胞周期蛋白D1和细胞周期蛋白E的表达与WHO分类中的乳头状或管状类型以及Lauren分类中的肠型呈正相关。p21、细胞周期蛋白D1和细胞周期蛋白E的表达与pT分期、淋巴结转移、血管及淋巴管侵犯等参数之间未发现显著相关性。关于生存情况,即使根据pT和pN分期以及Lauren分类对不同亚组患者进行单独分析,也未证实p21、细胞周期蛋白D1和细胞周期蛋白E的表达对预后有影响。目前的数据表明,细胞周期蛋白D1、细胞周期蛋白E及其抑制剂p21均不能预测胃癌患者的生存情况,其免疫组织化学检测也不是识别可能处于较高风险亚组患者合适的工具。

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