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English: DNA replicative stress can be induced by various factors including ROS, insufficient dNTP, oncogene activation or the loss/inactivation of tumor suppressors, etc. At the low to mild level, the replicative stress predominantly induces genomic instability, therefore facilitates tumorigenesis and cancer progression. However, when the replicative stress is enhanced to a high level through further loss of checkpoints, cancer cells may enter the mitotic phase with incomplete or uncorrected DNA replication, which eventually leads to cell death through mitotic catastrophe. Therefore, enhancing replicative stress can be a novel approach to kill cancer cells. TSG: Tumor suppressing gene.[1]
Date
Source https://doi.org/10.3390/genes7080051
Author Jun Zhang, Qun Dai, Dongkyoo Park, and Xingming Deng

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Rationale for enhancing replication stress to kill cancer cells

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19 August 2016

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current22:36, 24 May 2020Thumbnail for version as of 22:36, 24 May 20202,200 × 1,100 (648 KB)Rob HurtUploaded a work by Jun Zhang, Qun Dai, Dongkyoo Park, and Xingming Deng from https://doi.org/10.3390/genes7080051 with UploadWizard

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