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Inhibitors of emerging epigenetic targets for cancer therapy: a patent review (2010-2014)

机译:新兴的表观遗传学靶点抑制剂用于癌症治疗:一项专利审查(2010-2014年)

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摘要

Gene regulatory pathways comprise an emerging and active area of chemical probe discovery and investigational drug development. Emerging insights from cancer genome sequencing and chromatin biology have identified leveraged opportunities for development of chromatin-directed small molecules as cancer therapies. At present, only six agents in two epigenetic target classes have been approved by the US FDA, limited to treatment of hematological malignancies. Recently, new classes of epigenetic inhibitors have appeared in literatures. First-in-class compounds have successfully transitioned to clinical investigation, importantly also in solid tumors and pediatric malignancies. This review considers patent applications for small-molecule inhibitors of selected epigenetic targets from 2010 to 2014. Included are exemplary classes of chromatin-associated epigenomic writers (DOT1L and EZH2), erasers (LSD1) and readers (BRD4).
机译:基因调控途径包括化学探针发现和研究药物开发的新兴和活跃领域。癌症基因组测序和染色质生物学的新兴见解已经确定了利用染色质定向小分子开发癌症的杠杆机会。目前,美国FDA仅批准了两种表观遗传学目标类别中的六种药物,仅限于血液系统恶性肿瘤的治疗。最近,文献中出现了新型的表观遗传抑制剂。一流的化合物已成功过渡到临床研究,重要的是还用于实体瘤和小儿恶性肿瘤。这篇综述考虑了从2010年到2014年选定表观遗传学目标的小分子抑制剂的专利申请。其中包括与染色质相关的表观基因组作者(DOT1L和EZH2),橡皮擦(LSD1)和阅读器(BRD4)的示例类别。

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