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Epigenetic treatment of solid tumours: a review of clinical trials

机译:表观遗传治疗实体瘤:临床试验综述

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Epigenetic treatment has been approved by regulatory agencies for haematological malignancies. The success observed in cutaneous lymphomas represents a proof of principle that similar results may be obtained in solid tumours. Several agents that interfere with DNA methylation-demethylation and histones acetylation/deacetylation have been studied, and some (such as azacytidine, decitabine, valproic acid and vorinostat) are already in clinical use.The aim of this review is to provide a brief overview of the molecular events underlying the antitumour effects of epigenetic treatments and to summarise data available on clinical trials that tested the use of epigenetic agents against solid tumours. We not only list results but also try to indicate how the proper evaluation of this treatment might result in a better selection of effective agents and in a more rapid development.We divided compounds in demethylating agents and HDAC inhibitors. For each class, we report the antitumour activity and the toxic side effects. When available, we describe plasma pharmacokinetics and pharmacodynamic evaluation in tumours and in surrogate tissues (generally white blood cells).Epigenetic treatment is a reality in haematological malignancies and deserves adequate attention in solid tumours. A careful consideration of available clinical data however is required for faster drug development and possibly to re-evaluate some molecules that were perhaps discarded too early.
机译:表观遗传学治疗已被监管机构批准用于血液系统恶性肿瘤。在皮肤淋巴瘤中观察到的成功代表原理的证明,即在实体瘤中可以获得类似的结果。已经研究了几种干扰DNA甲基化-脱甲基化和组蛋白乙酰化/脱乙酰化的药物,其中一些已经在临床上使用(例如氮杂胞苷,地西他滨,丙戊酸和伏立诺他),本文的目的是简要概述表观遗传治疗的抗肿瘤作用的分子事件,并总结可用于测试表观遗传药物对抗实体瘤的临床试验的可用数据。我们不仅列出结果,而且尝试指出对这种治疗方法的正确评估可能如何导致更好地选择有效药物和更快地发展。我们将化合物分为去甲基化剂和HDAC抑制剂。对于每个类别,我们报告其抗肿瘤活性和毒性副作用。如果可以的话,我们描述了在肿瘤和替代组织(通常是白细胞)中的血浆药代动力学和药效学评价。表观遗传治疗在血液系统恶性肿瘤中是一种现实,在实体瘤中应引起足够的重视。但是,需要仔细考虑可用的临床数据,以加快药物开发的速度,并可能需要重新评估一些可能为时过早丢弃的分子。

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