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尿路上皮癌的表观遗传治疗选择

Epigenetic Treatment Options in Urothelial Carcinoma.

作者信息

Pinkerneil Maria, Hoffmann Michèle J, Niegisch Günter

机构信息

Department of Urology, Medical Faculty, Heinrich Heine University Düsseldorf, Gebäude 13.72, Moorenstraße 5, Düsseldorf, Germany.

出版信息

Methods Mol Biol. 2018;1655:289-317. doi: 10.1007/978-1-4939-7234-0_21.

Abstract

Mutations, dysregulation, and dysbalance of epigenetic regulators are especially frequent in urothelial carcinoma (UC) compared to other malignancies. Accordingly, targeting epigenetic regulators may provide a window of opportunity particularly in anticancer therapy of UC. In general, these epigenetic regulators comprise DNA methyltransferases and DNA demethylases (for DNA methylation), histone methyltransferases, and histone demethylases (for histone methylation) as well as acetyl transferases and histone deacetylases (for histone and non-histone acetylation).As epigenetic regulators target a plethora of cellular functions and available inhibitors often inhibit enzymatic activity of more than one isoenzyme or may have further off-target effects, analysis of their functions in UC pathogenesis as well as of the antineoplastic capacity of according inhibitors should follow a multidimensional approach.Here, we present our standard approach for the analysis of the cellular and molecular functions of individual HDAC enzymes, their suitability as treatment targets and for the evaluation of isoenzyme-specific HDAC inhibitors regarding their antineoplastic efficacy. This approach may also serve as prototype for the preclinical evaluation of other epigenetic treatment approaches.

摘要

与其他恶性肿瘤相比,表观遗传调控因子的突变、失调和失衡在尿路上皮癌(UC)中尤为常见。因此,靶向表观遗传调控因子可能提供一个机会之窗,特别是在UC的抗癌治疗中。一般来说,这些表观遗传调控因子包括DNA甲基转移酶和DNA去甲基化酶(用于DNA甲基化)、组蛋白甲基转移酶和组蛋白去甲基化酶(用于组蛋白甲基化)以及乙酰转移酶和组蛋白脱乙酰酶(用于组蛋白和非组蛋白乙酰化)。由于表观遗传调控因子针对大量细胞功能,且现有的抑制剂通常会抑制一种以上同工酶的酶活性,或者可能有其他脱靶效应,因此分析它们在UC发病机制中的功能以及相应抑制剂的抗肿瘤能力应采用多维度方法。在此,我们展示了分析单个HDAC酶的细胞和分子功能的标准方法、它们作为治疗靶点的适用性,以及评估同工酶特异性HDAC抑制剂的抗肿瘤疗效。这种方法也可作为其他表观遗传治疗方法临床前评估的原型。

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