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通过R环诱导DNA损伤以杀死癌细胞。

Inducing DNA damage through R-loops to kill cancer cells.

作者信息

Lam Fred C, Kong Yi Wen, Yaffe Michael B

机构信息

Division of Neurosurgery, Hamilton General Hospital, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.

Center for Precision Cancer Medicine at MIT, Cambridge, MA, USA.

出版信息

Mol Cell Oncol. 2020 Nov 20;8(1):1848233. doi: 10.1080/23723556.2020.1848233.

Abstract

R-loops are intermediate structures of transcription that can accumulate when transcriptional elongation is blocked by inhibiting BRD4. In normal cells, R-loop persistence suppresses firing of adjacent replication origins. This control is lost in a subset of cancer cells, where BRD4 inhibition results in R-loop accumulation, leading to transcription-replication collisions and DNA double-strand breaks during S-phase, followed by cell death. This finding sheds new light on the mechanisms by which BRD4 inhibitors function as cancer therapies, and indicates that targeting other cellular events to cause R-loop accumulation may be useful for cancer treatment.

摘要

R环是转录的中间结构,当通过抑制BRD4阻断转录延伸时,R环会积累。在正常细胞中,R环的持续存在会抑制相邻复制起点的激发。在一部分癌细胞中这种控制机制丧失,BRD4抑制导致R环积累,进而在S期引发转录-复制碰撞和DNA双链断裂,随后导致细胞死亡。这一发现为BRD4抑制剂作为癌症治疗药物的作用机制提供了新的线索,并表明靶向其他细胞事件以导致R环积累可能对癌症治疗有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6651/7849686/4d708b156434/KMCO_A_1848233_F0001_OC.jpg

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