利用天然化合物靶向表观遗传 "阅读器",拦截癌症。

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2020-12-30 DOI:10.15430/JCP.2020.25.4.189
Elisabetta Damiani, Munevver N Duran, Nivedhitha Mohan, Praveen Rajendran, Roderick H Dashwood
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引用次数: 0

摘要

来自不同来源的天然化合物,包括植物药和常见的食品和饮料,通过在疾病发病过程中影响表观基因组和基因表达的机制,发挥有益健康的作用。通过针对所谓的表观遗传 "阅读者"、"书写者 "和 "擦除者",膳食中的植物化学物质可以逆转癌细胞和肿瘤前期的异常表观基因组特征。因此,这类制剂为通过预防或治疗/治疗策略拦截癌症提供了途径。迄今为止,人们对膳食制剂的关注主要集中在写入剂(如组蛋白乙酰转移酶)和清除剂(如组蛋白去乙酰化酶)上,对表观遗传读取剂(如 BRD 蛋白)的关注较少。药物 JQ1 是作为表观遗传阅读器抑制剂的原型而开发的,它选择性地靶向溴化结构域和外端结构域(BET)家族的成员,如 BRD4。使用 JQ1 作为单药或与标准疗法联用的临床试验显示,该药具有抗肿瘤疗效,但并非没有毒性或耐药性。为了寻找第二代表观遗传读取器抑制剂,人们已将注意力转移到天然来源,包括可能被重新用作 "类 JQ1 "生物活性物质的膳食制剂。本综述总结了以天然化合物作为 BET 和其他表观遗传 "阅读器 "蛋白抑制剂的新兴研究活动的现状,并展望了未来的研究方向和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Targeting Epigenetic 'Readers' with Natural Compounds for Cancer Interception.

Natural compounds from diverse sources, including botanicals and commonly consumed foods and beverages, exert beneficial health effects via mechanisms that impact the epigenome and gene expression during disease pathogenesis. By targeting the so-called epigenetic 'readers', 'writers', and 'erasers', dietary phytochemicals can reverse abnormal epigenome signatures in cancer cells and preneoplastic stages. Thus, such agents provide avenues for cancer interception via prevention or treatment/therapeutic strategies. To date, much of the focus on dietary agents has been directed towards writers (e.g., histone acetyltransferases) and erasers (e.g., histone deacetylases), with less attention given to epigenetic readers (e.g., BRD proteins). The drug JQ1 was developed as a prototype epigenetic reader inhibitor, selectively targeting members of the bromodomain and extraterminal domain (BET) family, such as BRD4. Clinical trials with JQ1 as a single agent, or in combination with standard of care therapy, revealed antitumor efficacy but not without toxicity or resistance. In pursuit of second-generation epigenetic reader inhibitors, attention has shifted to natural sources, including dietary agents that might be repurposed as 'JQ1-like' bioactives. This review summarizes the current status of nascent research activity focused on natural compounds as inhibitors of BET and other epigenetic 'reader' proteins, with a perspective on future directions and opportunities.

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