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首页> 外文期刊>Oncogene >The tumor suppressor gene rap1GAP is silenced by miR-101-mediated EZH2 overexpression in invasive squamous cell carcinoma
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The tumor suppressor gene rap1GAP is silenced by miR-101-mediated EZH2 overexpression in invasive squamous cell carcinoma

机译:在侵袭性鳞状细胞癌中,miR-101介导的EZH2过表达使肿瘤抑制基因rap1GAP沉默

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摘要

Rap1GAP is a critical tumor suppressor gene that is downregulated in multiple aggressive cancers, such as head and neck squamous cell carcinoma, melanoma and pancreatic cancer. However, the mechanistic basis of rap1GAP downregulation in cancers is poorly understood. By employing an integrative approach, we demonstrate polycomb-mediated repression of rap1GAP that involves Enhancer of Zeste Homolog 2 (EZH2), a histone methyltransferase in head and neck cancers. We further demonstrate that the loss of miR-101 expression correlates with EZH2 upregulation, and the concomitant downregulation of rap1GAP in head and neck cancers. EZH2 represses rap1GAP by facilitating the trimethylation of histone 3 at lysine 27, a mark of gene repression, and also hypermethylation of rap1GAP promoter. These results provide a conceptual framework involving a microRNA鈥搊ncogene鈥搕umor suppressor axis to understand head and neck cancer progression.
机译:Rap1GAP是一个关键的肿瘤抑制基因,在多种侵袭性癌症中被下调,例如头颈部鳞状细胞癌,黑素瘤和胰腺癌。然而,人们对rap1GAP下调在癌症中的机制基础了解甚少。通过采用整合的方法,我们证明了涉及Zeste同源2(EZH2)增强子的多梳介导的rap1GAP抑制,这是头颈癌中的组蛋白甲基转移酶。我们进一步证明,miR-101表达的丧失与EZH2上调以及rap1GAP在头颈癌中的下调相关。 EZH2通过促进赖氨酸27处组蛋白3的三甲基化(基因抑制的标志)和rap1GAP启动子的高甲基化来抑制rap1GAP。这些结果提供了涉及microRNA“癌基因”抑癌轴的概念框架,以了解头颈癌的进展。

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