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解读组蛋白去乙酰化酶抑制剂的临床检测。

Interpreting clinical assays for histone deacetylase inhibitors.

机构信息

Laboratory of Bioactive Molecules, Institute of Chemistry, University of Nice - Sophia Antipolis, Parc Valrose, Nice, France;

出版信息

Cancer Manag Res. 2011;3:117-41. doi: 10.2147/CMR.S9661. Epub 2011 May 9.

Abstract

As opposed to genetics, dealing with gene expressions by direct DNA sequence modifications, the term epigenetics applies to all the external influences that target the chromatin structure of cells with impact on gene expression unrelated to the sequence coding of DNA itself. In normal cells, epigenetics modulates gene expression through all development steps. When "imprinted" early by the environment, epigenetic changes influence the organism at an early stage and can be transmitted to the progeny. Together with DNA sequence alterations, DNA aberrant cytosine methylation and microRNA deregulation, epigenetic modifications participate in the malignant transformation of cells. Their reversible nature has led to the emergence of the promising field of epigenetic therapy. The efforts made to inhibit in particular the epigenetic enzyme family called histone deacetylases (HDACs) are described. HDAC inhibitors (HDACi) have been proposed as a viable clinical therapeutic approach for the treatment of leukemia and solid tumors, but also to a lesser degree for noncancerous diseases. Three epigenetic drugs are already arriving at the patient's bedside, and more than 100 clinical assays for HDACi are registered on the National Cancer Institute website. They explore the eventual additive benefits of combined therapies. In the context of the pleiotropic effects of HDAC isoforms, more specific HDACi and more informative screening tests are being developed for the benefit of the patients.

摘要

与直接通过 DNA 序列修饰来处理基因表达的遗传学不同,表观遗传学适用于所有针对细胞染色质结构的外部影响,这些影响会影响基因表达,而与 DNA 自身的编码序列无关。在正常细胞中,表观遗传学通过所有发育步骤来调节基因表达。当早期受到环境的“印记”时,表观遗传变化会在早期影响生物体,并可以传递给后代。与 DNA 序列改变、DNA 异常胞嘧啶甲基化和 microRNA 失调一起,表观遗传修饰参与了细胞的恶性转化。它们的可逆性质导致了有前途的表观遗传治疗领域的出现。描述了抑制特别是称为组蛋白去乙酰化酶 (HDAC) 的表观遗传酶家族的努力。HDAC 抑制剂 (HDACi) 已被提议作为治疗白血病和实体瘤的可行临床治疗方法,但在治疗非癌症疾病方面的效果也较小。三种表观遗传药物已经到达患者床边,并且在国立癌症研究所网站上注册了超过 100 种用于 HDACi 的临床检测。它们探索了联合治疗的潜在附加益处。在 HDAC 同工型的多效性效应的背景下,正在为患者的利益开发更特异的 HDACi 和更具信息量的筛选试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/580e2504a3c7/cmr-3-117f1.jpg

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