Tse Archie N, Carvajal Richard, Schwartz Gary K
Authors' Affiliations: Gastrointestinal Oncology Service and Melanoma and Sarcoma Service, Division of Solid Tumor Oncology and Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York.
Clin Cancer Res. 2007 Apr 1;13(7):1955-60. doi: 10.1158/1078-0432.CCR-06-2793.
Progression through the cell cycle is monitored by surveillance mechanisms known as cell cycle checkpoints. Our knowledge of the biochemical nature of checkpoint regulation during an unperturbed cell cycle and following DNA damage has expanded tremendously over the past decade. We now know that dysfunction in cell cycle checkpoints leads to genomic instability and contributes to tumor progression, and most agents used for cancer therapy, such as cytotoxic chemotherapy and ionizing radiation, also activate cell cycle checkpoints. Understanding how checkpoints are regulated is therefore important from the points of view of both tumorigenesis and cancer treatment. In this review, we present an overview of the molecular hierarchy of the checkpoint signaling network and the emerging role of checkpoint targets, especially checkpoint kinase 1, in cancer therapy. Further, we discuss the results of recent clinical trials involving the nonspecific checkpoint kinase 1 inhibitor, UCN-01, and the challenges we face with this new therapeutic approach.
细胞周期进程受称为细胞周期检查点的监测机制调控。在过去十年中,我们对正常细胞周期及DNA损伤后检查点调控的生化本质的认识有了极大扩展。我们现在知道,细胞周期检查点功能失调会导致基因组不稳定并促进肿瘤进展,而且大多数用于癌症治疗的药物,如细胞毒性化疗药物和电离辐射,也会激活细胞周期检查点。因此,从肿瘤发生和癌症治疗的角度来看,了解检查点如何被调控都很重要。在本综述中,我们概述了检查点信号网络的分子层级以及检查点靶点,尤其是检查点激酶1在癌症治疗中的新作用。此外,我们讨论了近期涉及非特异性检查点激酶1抑制剂UCN - 01的临床试验结果以及这种新治疗方法面临的挑战。