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首页> 外文期刊>Journal of pharmacological sciences. >Drug Development Targeting the Glycogen Synthase Kinase-3β (GSK-3β)-Mediated Signal Transduction Pathway: Inhibitors of the Wnt/β-Catenin Signaling Pathway as Novel Anticancer Drugs
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Drug Development Targeting the Glycogen Synthase Kinase-3β (GSK-3β)-Mediated Signal Transduction Pathway: Inhibitors of the Wnt/β-Catenin Signaling Pathway as Novel Anticancer Drugs

机译:靶向糖原合酶激酶3β(GSK-3β)介导的信号传导途径的药物开发:Wnt /β-Catenin信号通路的抑制剂作为新型抗癌药物

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References(35) Cited-By(31) Accumulating evidence suggests that the Wnt/β-catenin signaling pathway is often involved in oncogenesis and cancer development. Accordingly, a novel anticancer drug can be developed using inhibitors of this pathway. However, at present, there is no selective inhibitor of this pathway available as a therapeutic agent. Although all the components of the Wnt/β-catenin signaling pathway can be a target for drug development, glycogen synthase kinase-3β (GSK-3β), in particular, may be a good target because GSK-3β is an essential component of the pathway, and activation of this kinase results in the inhibition of the Wnt signaling pathway. We found that the differentiation-inducing factors (DIFs), putative morphogens for Dictyostelium discoideum, inhibit the Wnt/β-catenin signaling pathway via the activation of GSK-3β, resulting in the cell-cycle arrest of human cancer cell lines. In this review, we summarize our recent findings on the antiproliferative effect of DIFs and show the possibility for development of a novel anticancer drug from DIFs and their derivatives.
机译:参考文献(35)Cited-By(31)越来越多的证据表明,Wnt /β-catenin信号通路通常与肿瘤发生和癌症发展有关。因此,可以使用该途径的抑制剂来开发新型抗癌药。但是,目前尚无该途径的选择性抑制剂可作为治疗剂。尽管Wnt /β-catenin信号传导途径的所有成分都可以成为药物开发的靶标,但糖原合酶激酶3β(GSK-3β)尤其可以作为良好的靶标,因为GSK-3β是糖原合成酶必不可少的成分。途径,该激酶的激活导致Wnt信号通路的抑制。我们发现分化诱导因子(DIFs),盘基网柄菌的假定形态发生子,通过激活GSK-3β抑制Wnt /β-catenin信号通路,从而导致人癌细胞株的细胞周期停滞。在这篇综述中,我们总结了我们对DIFs的抗增殖作用的最新发现,并显示了从DIFs及其衍生物开发新型抗癌药物的可能性。

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