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Epigenetic modification in the expression of p73 p73 - epigenetic target for anticancer therapy

机译:表观遗传学修饰p73 p73-表观遗传靶标用于抗癌治疗

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摘要

A p73 is a new member of p53 family of transcription factor, having two types. First is TAp73, transcriptionally active and expressed via upstream promoter as a tumor suppressor and vital apoptotic inductor, it also has a key role in cell cycle arrest/differentiation and Second is ΔNp73 that is transcriptionally inactive and expressed via downstream regulator as oncogenes. Both types are expressed in various isoforms, which originate from alternative splicing events at the C-terminus. Upon DNA damage, posttranslational modifications cause conformational changes in various amino acid residues via induction or inhibition of various proteins, which are present in the structural domains of p73. These modifications may cause up- or down-regulation of p73 expression levels, as well as alters the transcriptional activity and/or stability of the protein. In this review, we have made an effort to assemble all existing data regarding the role of p73, its modification and after effects in cancer.
机译:p73是转录因子p53家族的新成员,具有两种类型。首先是TAp73,转录激活并通过上游启动子表达为肿瘤抑制因子和重要的凋亡诱导剂,它在细胞周期阻滞/分化中也起关键作用,其次是ΔNp73,它在转录上无活性并通过下游调节剂表达为癌基因。两种类型均以各种同工型表达,这些同工型源自C末端的可变剪接事件。 DNA受损后,翻译后修饰会通过诱导或抑制p73结构域中存在的各种蛋白质,导致各种氨基酸残基的构象变化。这些修饰可能导致p73表达水平的上调或下调,以及改变蛋白质的转录活性和/或稳定性。在这项审查中,我们已努力收集有关p73的作用,其修饰和在癌症中的后效应的所有现有数据。

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