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细胞周期蛋白依赖性激酶抑制剂改变在人类癌症中的预后意义。

The prognostic significance of altered cyclin-dependent kinase inhibitors in human cancer.

作者信息

Tsihlias J, Kapusta L, Slingerland J

机构信息

Department of Urology, Sunnybrook Health Science Centre, University of Toronto, Ontario, Canada.

出版信息

Annu Rev Med. 1999;50:401-23. doi: 10.1146/annurev.med.50.1.401.

Abstract

Progression through the cell cycle is governed by cyclin-dependent kinases (cdks), whose activity is inhibited by the cdk inhibitors. Cyclins, cdks, and cdk inhibitors are frequently deregulated in cancers. This chapter reviews the prognostic significance of alterations in cdk inhibitors. Loss of p27 protein provides independent prognostic information in breast, prostate, colon, and gastric carcinomas, and immunohistochemical (IHC) staining for p27 may eventually become part of routine histopathologic processing of cancers. Loss of IHC staining for p21 may be prognostic in certain cancers but conflicting results are reported in breast cancer. Reports on homozygous deletion of p16 and p15 genes suggest the value of larger, prospective studies with standardized treatment protocols to definitively establish the prognostic utility of p15/p16 deletions in acute leukemias. Larger trials and the development of a consensus on methods for deletion analysis, IHC staining, and tumor scoring will be needed to move these molecular assays from bench to bedside.

摘要

细胞周期的进程受细胞周期蛋白依赖性激酶(cdks)调控,其活性受到cdk抑制剂的抑制。细胞周期蛋白、cdks和cdk抑制剂在癌症中经常失调。本章综述了cdk抑制剂改变的预后意义。p27蛋白的缺失在乳腺癌、前列腺癌、结肠癌和胃癌中提供独立的预后信息,p27的免疫组织化学(IHC)染色最终可能成为癌症常规组织病理学处理的一部分。p21的IHC染色缺失在某些癌症中可能具有预后意义,但乳腺癌的报道结果相互矛盾。关于p16和p15基因纯合缺失的报告表明,需要开展更大规模的、采用标准化治疗方案的前瞻性研究,以明确确定p15/p16缺失在急性白血病中的预后效用。需要进行更大规模的试验,并就缺失分析、IHC染色和肿瘤评分方法达成共识,以便将这些分子检测从实验室应用到临床。

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