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Absence of p53 Enhances Growth Defects and Etoposide Sensitivity of Human Cells Lacking the Bloom Syndrome Helicase BLM

机译:缺少p53会增强缺乏Bloom综合征解旋酶BLM的人细胞的生长缺陷和依托泊苷的敏感性。

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摘要

The Bloom syndrome helicase BLM and the tumor-suppressor protein p53 play important roles in preserving genome integrity. Here, we knock out the genes for BLM and p53 in a human pre-B-cell line, Nalm-6. We show that p53 plays an important role in cell proliferation, but not apoptosis, when BLM is absent. Intriguingly, despite the apoptotic function of p53, BLM−/−TP53−/− cells were more sensitive than either single mutant to etoposide, an anticancer agent that poisons DNA topoisomerase II. Our results suggest a direct, BLM-independent role for p53 in etoposide-induced, topoisomerase II–mediated DNA damage in human cells.
机译:Bloom综合征解旋酶BLM和肿瘤抑制蛋白p53在保持基因组完整性中起重要作用。在这里,我们敲除人类前B细胞系Nalm-6中BLM和p53的基因。我们显示,当BLM缺失时,p53在细胞增殖中起重要作用,但在细胞凋亡中不起作用。有趣的是,尽管p53具有凋亡功能,但BLM-/-TP53-/-细胞对依托泊苷(一种使DNA拓扑异构酶II中毒的抗癌药)比单个突变体更为敏感。我们的结果表明,p53在依托泊苷诱导的拓扑异构酶II介导的人类细胞DNA损伤中具有直接的,不依赖BLM的作用。

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