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Ets-1 蛋白的水平受聚(ADP-核糖)聚合酶-1(PARP-1)在癌细胞中的调控,以防止 DNA 损伤。

The level of Ets-1 protein is regulated by poly(ADP-ribose) polymerase-1 (PARP-1) in cancer cells to prevent DNA damage.

机构信息

CNRS USR 3078, Institut de Recherche Interdisciplinaire, Campus CNRS de la Haute Borne, Université Lille Nord de France, IFR 147, BP 70478, Villeneuve d'Ascq, France.

出版信息

PLoS One. 2013;8(2):e55883. doi: 10.1371/journal.pone.0055883. Epub 2013 Feb 6.

Abstract

Ets-1 is a transcription factor that regulates many genes involved in cancer progression and in tumour invasion. It is a poor prognostic marker for breast, lung, colorectal and ovary carcinomas. Here, we identified poly(ADP-ribose) polymerase-1 (PARP-1) as a novel interaction partner of Ets-1. We show that Ets-1 activates, by direct interaction, the catalytic activity of PARP-1 and is then poly(ADP-ribosyl)ated in a DNA-independent manner. The catalytic inhibition of PARP-1 enhanced Ets-1 transcriptional activity and caused its massive accumulation in cell nuclei. Ets-1 expression was correlated with an increase in DNA damage when PARP-1 was inhibited, leading to cancer cell death. Moreover, PARP-1 inhibitors caused only Ets-1-expressing cells to accumulate DNA damage. These results provide new insight into Ets-1 regulation in cancer cells and its link with DNA repair proteins. Furthermore, our findings suggest that PARP-1 inhibitors would be useful in a new therapeutic strategy that specifically targets Ets-1-expressing tumours.

摘要

Ets-1 是一种转录因子,可调节许多参与癌症进展和肿瘤侵袭的基因。它是乳腺癌、肺癌、结直肠癌和卵巢癌的预后不良标志物。在这里,我们确定多聚(ADP-核糖)聚合酶 1(PARP-1)是 Ets-1 的一种新型相互作用伙伴。我们表明,Ets-1 通过直接相互作用激活 PARP-1 的催化活性,然后以非依赖于 DNA 的方式进行多聚(ADP-核糖)化。PARP-1 的催化抑制增强了 Ets-1 的转录活性,并导致其大量积累在细胞核中。当抑制 PARP-1 时,Ets-1 的表达与 DNA 损伤的增加相关,导致癌细胞死亡。此外,PARP-1 抑制剂仅使表达 Ets-1 的细胞积累 DNA 损伤。这些结果为癌细胞中 Ets-1 的调节及其与 DNA 修复蛋白的联系提供了新的见解。此外,我们的研究结果表明,PARP-1 抑制剂将在一种新的治疗策略中非常有用,该策略专门针对表达 Ets-1 的肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fb2/3566071/a103d40fe2e8/pone.0055883.g001.jpg

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