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p27kip1在乳腺癌中的表达及其预后意义。

Expression of p27kip1 in breast cancer and its prognostic significance.

作者信息

Barnes A, Pinder S E, Bell J A, Paish E C, Wencyk P M, Robertson J F R, Elston C W, Ellis I O

机构信息

Department of Histopathology, Nottingham City Hospital Breast Unit, Nottingham, UK.

出版信息

J Pathol. 2003 Nov;201(3):451-9. doi: 10.1002/path.1464.

Abstract

p27kip1 is a member of the KIP/CIP family of cyclin-dependent kinase inhibitors and is a negative cell-cycle regulator that is thought to play a role in tumour suppression. Reduced levels of this protein have been observed in a number of human cancers. However, evidence is conflicting as to whether p27kip1 has a role to play in breast cancer, including predicting behaviour and prognosis. The present investigation aimed to provide a definitive study of 830 breast cancer cases with median patient follow-up of 104 months to determine the true prognostic significance, if any. Immunohistochemical analysis of tissue microarrays and three scoring methods were used to assess p27kip1 expression. Univariate analysis showed a significant relationship between reduced p27kip1 expression and increasing tumour grade, nuclear pleomorphism, mitosis, and decreasing tubule formation (all p<0.001). Significant associations between reduced p27, negative oestrogen receptor status, and ductal/no special type tumours were also observed. Survival analysis demonstrated that patients with tumours with high p27kip1 levels had an improved survival compared with those with cancers with low expression. On multivariate analysis, when compared with existing factors, p27kip1 was not, however, an independent prognostic factor. It is concluded that the inverse relationship between p27kip1 levels and histological grade and individual grade components suggests a role for p27kip1 in both cell proliferation and differentiation, but is not clinically useful.

摘要

p27kip1是细胞周期蛋白依赖性激酶抑制剂KIP/CIP家族的成员,是一种负性细胞周期调节因子,被认为在肿瘤抑制中发挥作用。在许多人类癌症中都观察到这种蛋白水平降低。然而,关于p27kip1在乳腺癌中是否发挥作用,包括预测其行为和预后,证据存在矛盾。本研究旨在对830例乳腺癌病例进行确定性研究,患者中位随访时间为104个月,以确定其真正的预后意义(如果有的话)。使用组织微阵列的免疫组织化学分析和三种评分方法来评估p27kip1的表达。单变量分析显示,p27kip1表达降低与肿瘤分级增加、核多形性、有丝分裂增加以及小管形成减少之间存在显著相关性(所有p<0.001)。还观察到p27降低、雌激素受体阴性状态与导管/非特殊类型肿瘤之间存在显著关联。生存分析表明,p27kip1水平高的肿瘤患者与低表达癌症患者相比,生存率有所提高。然而,在多变量分析中,与现有因素相比,p27kip1并不是一个独立的预后因素。结论是,p27kip1水平与组织学分级及各个分级成分之间的负相关关系表明p27kip1在细胞增殖和分化中均起作用,但在临床上并无用处。

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