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5-氮杂胞苷/氮杂胞苷

5-Azacytidine/Azacitidine.

作者信息

Müller Antonia, Florek Mareike

机构信息

Division of Blood and Marrow Transplantation, Stanford University, School of Medicine, 269, West Campus Drive CCSR, Stanford, CA 94305, USA.

出版信息

Recent Results Cancer Res. 2010;184:159-70. doi: 10.1007/978-3-642-01222-8_11.

Abstract

5-Azacytidine is a pyrimidine nucleoside analog that has been discovered more than 40 years ago. Despite remarkable responses in the treatment of acute myeloid leukemias in the 1970s no earlier than 2004 has this agent been approved by the US FDA for the treatment of all subtypes of myelodysplatic syndromes (MDS). For the first time a drug was proven to alter the natural course of MDS, as demonstrated in three clinical trials conducted by the CALG B. Complete remission rates ranged between 10-17%, and more recently, a significant survival benefit for MDS patients treated with 5-Azacytidine could be established. The antineoplastic activity is due to incorporation into RNA with disruption of RNA metabolism, and inhibition of DNA methylation.Strategies of combining epigenetic manipulation with other 'new' drugs aim at increasing the efficacy of the hypomethylating agents. Particularly histone deacetylase inhibitors have been deemed useful therapeutic partners, and preliminary results are promising.

摘要

5-氮杂胞苷是一种嘧啶核苷类似物,40多年前就已被发现。尽管在20世纪70年代治疗急性髓系白血病时取得了显著疗效,但直到2004年该药物才被美国食品药品监督管理局批准用于治疗所有亚型的骨髓增生异常综合征(MDS)。首次有药物被证明能改变MDS的自然病程,这在CALGB进行的三项临床试验中得到了证实。完全缓解率在10%至17%之间,最近,使用5-氮杂胞苷治疗的MDS患者有显著的生存获益得以确立。其抗肿瘤活性是由于掺入RNA并破坏RNA代谢以及抑制DNA甲基化。将表观遗传调控与其他“新型”药物联合使用的策略旨在提高去甲基化药物的疗效。特别是组蛋白去乙酰化酶抑制剂已被认为是有用的治疗搭档,初步结果很有前景。

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