首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >The Ubiquitin Ligase Siah2 Regulates Tumorigenesis And Metastasis By Hif-dependent And -independent Pathways
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The Ubiquitin Ligase Siah2 Regulates Tumorigenesis And Metastasis By Hif-dependent And -independent Pathways

机译:泛素连接酶Siah2通过Hif依赖性和非依赖性途径调节肿瘤发生和转移

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The ubiquitin ligase Siah2 has been shown to regulate prolyl hydroxylase 3 (PHD3) stability with concomitant effect on HIF-1α availability. Because HIF-1α is implicated in tumorigenesis and metastasis, we used SW1 mouse melanoma cells, which develop primary tumors with a propensity to metastasize, in a syngeneic mouse model to assess a possible role for Siah2 in these processes. Inhibiting Siah2 activity by expressing a peptide designed to outcompete association of Siah2-interacting proteins reduced metastasis through HIF-1α without affecting tumorigenesis. Conversely, inhibiting Siah2 activity by means of a dominant-negative Siah2 RING mutant primarily reduced tumorigenesis through the action of Sprouty 2, a negative regulator of Ras signaling. Consistent with our findings, reduced expression of PHD3 and Sprouty2 was observed in more advanced stages of melanoma tumors. Using complementary approaches, our data establish the role of Siah2 in tumorigenesis and metastasis by HIF-dependent and -independent mechanisms.
机译:泛素连接酶Siah2已被证明可调节脯氨酰羟化酶3(​​PHD3)的稳定性,同时对HIF-1α的可用性产生影响。因为HIF-1α与肿瘤发生和转移有关,所以我们在同系小鼠模型中使用SW1小鼠黑色素瘤细胞(其发展出具有转移倾向的原发性肿瘤)来评估Siah2在这些过程中的可能作用。通过表达一种肽来抑制Siah2活性,该肽设计用于竞争与Siah2相互作用的蛋白的缔合,从而降低了通过HIF-1α的转移而不会影响肿瘤的发生。相反,通过显性阴性Siah2 RING突变体抑制Siah2活性,主要是通过Sprouty 2(Ras信号的负调节剂)的作用减少了肿瘤的发生。与我们的发现一致,在黑色素瘤肿瘤的更晚期阶段观察到PHD3和Sprouty2表达降低。使用补充方法,我们的数据通过HIF依赖性和非依赖性机制确立了Siah2在肿瘤发生和转移中的作用。

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