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首页> 外文期刊>Oncogene >Poly(ADP-ribose)-dependent regulation of Snail1 protein stability
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Poly(ADP-ribose)-dependent regulation of Snail1 protein stability

机译:聚(ADP-核糖)依赖的Snail1蛋白稳定性调节。

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摘要

Snail1 is a master regulator of the epithelial鈥搈esenchymal transition (EMT) and has been implicated in key tumor biological processes such as invasion and metastasis. It has been previously shown that poly(ADP-ribose) polymerase-1 (PARP-1) knockdown, but not PARP inhibition, downregulates the expression of Snail1. In this study we have characterized a novel regulatory mechanism controlling Snail1 protein expression through poly(ADP-ribosyl)ation. The effect is not only limited to repression of Snail1 transcription but also to downregulated Snail1 protein stability. PARP-1 (but not PARP-2) poly(ADP) ribosylates Snail1, both in vivo and in vitro , and interacts with Snail1, an association that is sensitive to PARP inhibitors. PARP inhibition has also clear effects on EMT phenotype of different tumor cells, including Snail1 downregulation, E-cadherin upregulation, decreased cell elongation and invasiveness. Therefore, this study reveals a new regulatory mechanism of Snail1 activation through poly(ADP-ribosyl)ation with consequences in malignant transformation through EMT.
机译:Snail1是上皮-间充质转化(EMT)的主要调节剂,已参与关键的肿瘤生物学过程,例如侵袭和转移。以前已经表明,聚(ADP-核糖)聚合酶-1(PARP-1)敲低,但不是PARP抑制,下调Snail1的表达。在这项研究中,我们已经表征了一种通过聚(ADP-核糖基)化控制Snail1蛋白表达的新型调控机制。该作用不仅限于Snail1转录的抑制,而且还限于Snail1蛋白稳定性的下调。 PARP-1(而非PARP-2)聚(ADP)核糖基使Snail1体内和体外均与Snail1相互作用,并且与Snail1相互作用(对PARP抑制剂敏感)。 PARP抑制对不同肿瘤细胞的EMT表型也有明显影响,包括Snail1下调,E-钙粘蛋白上调,细胞伸长率降低和侵袭性降低。因此,本研究揭示了通过聚(ADP-核糖基)活化Snail1的新调控机制,并通过EMT导致恶性转化。

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