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细胞周期检查点机制:处于癌症发生与药物研发的交叉点

Mechanisms of cell-cycle checkpoints: at the crossroads of carcinogenesis and drug discovery.

作者信息

Flatt P M, Pietenpol J A

机构信息

Department of Biochemistry, Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

Drug Metab Rev. 2000 Aug-Nov;32(3-4):283-305. doi: 10.1081/dmr-100102335.

Abstract

Human tumors arise from multiple genetic changes that gradually transform growth-limited cells into highly invasive cells that are unresponsive to growth controls. The genetic evolution of normal cells into cancer cells is largely determined by the fidelity of DNA replication, repair, and division. Cell-cycle arrest in response to stress is integral to the maintenance of genomic integrity. The control mechanisms that restrain cell-cycle transition or induce apoptotic signaling pathways after cell stress are known as cell-cycle checkpoints. This review will focus on the mechanisms of cell-cycle checkpoint pathways and how different components of these pathways are frequently altered in the genesis of human tumors. As our knowledge of cell-cycle regulation and checkpoints increases, so will our understanding of how xenobiotic agents can affect these processes to either initiate or inhibit tumorigenesis.

摘要

人类肿瘤源于多种基因变化,这些变化逐渐将生长受限的细胞转变为对生长控制无反应的高度侵袭性细胞。正常细胞向癌细胞的基因进化在很大程度上取决于DNA复制、修复和分裂的保真度。对应激作出反应的细胞周期停滞对于维持基因组完整性至关重要。在细胞应激后抑制细胞周期过渡或诱导凋亡信号通路的控制机制被称为细胞周期检查点。本综述将聚焦于细胞周期检查点通路的机制,以及这些通路的不同组成部分在人类肿瘤发生过程中是如何频繁发生改变的。随着我们对细胞周期调控和检查点的了解不断增加,我们对异源生物制剂如何影响这些过程以启动或抑制肿瘤发生的理解也会随之加深。

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