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人类疾病发病机制与治疗中的拓扑异构酶I

Topoisomerase I in Human Disease Pathogenesis and Treatments.

作者信息

Li Min, Liu Yilun

机构信息

Department of Cancer Genetics and Epigenetics, Beckman Research Institute, City of Hope, Duarte, CA 91010-3000, USA.

Department of Cancer Genetics and Epigenetics, Beckman Research Institute, City of Hope, Duarte, CA 91010-3000, USA.

出版信息

Genomics Proteomics Bioinformatics. 2016 Jun;14(3):166-171. doi: 10.1016/j.gpb.2016.02.004. Epub 2016 May 12.

Abstract

Mammalian topoisomerase 1 (TOP1) is an essential enzyme for normal development. TOP1 relaxes supercoiled DNA to remove helical constraints that can otherwise hinder DNA replication and transcription and thus block cell growth. Unfortunately, this exact activity can covalently trap TOP1 on the DNA that could lead to cell death or mutagenesis, a precursor for tumorigenesis. It is therefore important for cells to find a proper balance between the utilization of the TOP1 catalytic activity to maintain DNA topology and the risk of accumulating the toxic DNA damages due to TOP1 trapping that prevents normal cell growth. In an apparent contradiction to the negative attribute of the TOP1 activity to genome stability, the detrimental effect of the TOP1-induced DNA lesions on cell survival has made this enzyme a prime target for cancer therapies to kill fast-growing cancer cells. In addition, cumulative evidence supports a direct role of TOP1 in promoting transcriptional progression independent of its topoisomerase activity. The involvement of TOP1 in transcriptional regulation has recently become a focus in developing potential new treatments for a subtype of autism spectrum disorders. Clearly, the impact of TOP1 on human health is multifold. In this review, we will summarize our current understandings on how TOP1 contributes to human diseases and how its activity is targeted for disease treatments.

摘要

哺乳动物拓扑异构酶1(TOP1)是正常发育所必需的酶。TOP1使超螺旋DNA松弛,以消除否则可能阻碍DNA复制和转录从而阻断细胞生长的螺旋限制。不幸的是,正是这种确切的活性可使TOP1共价捕获在DNA上,这可能导致细胞死亡或诱变,而诱变是肿瘤发生的前兆。因此,对于细胞而言,在利用TOP1催化活性维持DNA拓扑结构与因TOP1捕获而积累有毒DNA损伤从而阻止正常细胞生长的风险之间找到适当平衡非常重要。与TOP1活性对基因组稳定性的负面属性明显矛盾的是,TOP1诱导的DNA损伤对细胞存活的有害影响使该酶成为杀死快速生长癌细胞的癌症治疗的主要靶点。此外,越来越多的证据支持TOP1在促进转录进程中发挥直接作用,而与其拓扑异构酶活性无关。TOP1参与转录调控最近已成为开发针对自闭症谱系障碍一种亚型的潜在新疗法的焦点。显然,TOP1对人类健康的影响是多方面的。在本综述中,我们将总结我们目前对TOP1如何导致人类疾病以及其活性如何成为疾病治疗靶点的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f567/4936607/51c62dcb1dce/gr1.jpg

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