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Wogonin and related natural flavones are inhibitors of CDK9 that induce apoptosis in cancer cells by transcriptional suppression of Mcl-1

机译:Wogonin和相关的天然黄酮是CDK9抑制剂,可通过转录抑制Mcl-1诱导癌细胞凋亡

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The wogonin-containing herb Scutellaria baicalensis has successfully been used for curing various diseases in traditional Chinese medicine. Wogonin has been shown to induce apoptosis in different cancer cells and to suppress growth of human cancer xenografts in vivo. However, its direct targets remain unknown. In this study, we demonstrate for the first time that wogonin and structurally related natural flavones, for example, apigenin, chrysin and luteolin, are inhibitors of cyclin-dependent kinase 9 (CDK9) and block phosphorylation of the carboxy-terminal domain of RNA polymerase II at Ser2. This effect leads to reduced RNA synthesis and subsequently rapid downregulation of the short-lived anti-apoptotic protein myeloid cell leukemia 1 (Mcl-1) resulting in apoptosis induction in cancer cells. We show that genetic inhibition of Mcl-1 or CDK9 expression by siRNA is sufficient to mimic flavone-induced apoptosis. Pull-down and in silico docking studies demonstrate that wogonin directly binds to CDK9, presumably to the ATP-binding pocket. In contrast, wogonin does not inhibit CDK2, CDK4 and CDK6 at doses that inhibit CDK9 activity. Furthermore, we show that wogonin preferentially inhibits CDK9 in malignant compared with normal lymphocytes. Thus, our study reveals a new mechanism of anti-cancer action of natural flavones and supports CDK9 as a therapeutic target in oncology.. ? 2011 Macmillan Publishers Limited
机译:含有伍格宁的草药黄cut已成功用于治疗中药中的多种疾病。 Wogonin已显示在体​​内诱导不同癌细胞的凋亡并抑制人类异种移植物的生长。但是,其直接目标仍然未知。在这项研究中,我们首次证明了卵黄素和与结构相关的天然黄酮(例如芹菜素,chrysin和木犀草素)是细胞周期蛋白依赖性激酶9(CDK9)的抑制剂,并阻止RNA聚合酶羧基端结构域的磷酸化II在Ser 2 。这种作用导致减少的RNA合成,并随后迅速下调短暂的抗凋亡蛋白髓样细胞白血病1(Mcl-1),从而导致癌细胞凋亡。我们表明,siRNA对Mcl-1或CDK9表达的遗传抑制足以模拟黄酮诱导的细胞凋亡。下拉和计算机对接研究表明,wogonin直接与CDK9结合,大概与ATP结合袋结合。相反,wogonin在抑制CDK9活性的剂量下不抑制CDK2,CDK4和CDK6。此外,我们显示,与正常淋巴细胞相比,wogonin在恶性肿瘤中优先抑制CDK9。因此,我们的研究揭示了天然黄酮抗癌作用的新机制,并支持CDK9作为肿瘤学中的治疗靶标。 2011 Macmillan Publishers Limited

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