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癌症基因表达的拓扑异构酶调控

Topoisomerase Regulation of Cancer Gene Expression.

作者信息

Baranello Laura, Kouzine Fedor, Levens David

机构信息

Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden; email:

Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland, USA; emails:

出版信息

Annu Rev Biochem. 2025 Jun;94(1):333-359. doi: 10.1146/annurev-biochem-091724-010717. Epub 2025 Mar 18.

Abstract

Under hyperproliferative conditions, escalation of genomic activity provokes high levels of DNA mechanical stress. Cancer cells cope with this stress through topoisomerase activity. Topoisomerases support genome-wide programs, including those driven by oncogenes and tumor suppressors, by adjusting the supercoiling and by interacting with the regulatory complexes involved in transcription, replication, and chromatin transactions. Topoisomerases also manage DNA conformational alterations that control gene activity. However, when the topological stress from oncogene-driven processes exceeds topoisomerase capacity, aberrant structures associated with DNA damage arise. These abnormalities include R-loop formation during transcription and replication. Excessive supercoiling also creates transcription-replication conflicts triggering DNA damage. Topoisomerase catalytic failure elicits topological dysregulation and DNA damage. This damage contributes further to tumorigenesis and tumor progression. The roles of topoisomerases in various genetic processes have been widely described, but the cancer-specific functions of topoisomerases are incompletely understood. Here, we summarize the crucial roles played by topoisomerases in cancer.

摘要

在细胞过度增殖的情况下,基因组活性的增强会引发高水平的DNA机械应力。癌细胞通过拓扑异构酶活性来应对这种应力。拓扑异构酶通过调节超螺旋以及与参与转录、复制和染色质交易的调控复合物相互作用,支持全基因组程序,包括那些由癌基因和肿瘤抑制因子驱动的程序。拓扑异构酶还能处理控制基因活性的DNA构象改变。然而,当癌基因驱动过程产生的拓扑应力超过拓扑异构酶的能力时,就会出现与DNA损伤相关的异常结构。这些异常包括转录和复制过程中的R环形成。过度超螺旋还会引发转录-复制冲突,从而导致DNA损伤。拓扑异构酶催化失败会引发拓扑失调和DNA损伤。这种损伤会进一步促进肿瘤发生和肿瘤进展。拓扑异构酶在各种遗传过程中的作用已被广泛描述,但拓扑异构酶在癌症中的特异性功能尚未完全了解。在此,我们总结了拓扑异构酶在癌症中所起的关键作用。

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