Institute for RNA Medicine, Department of Pathology, Beth Israel Deaconess Medical Center Cancer Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
Nat Rev Drug Discov. 2017 Mar;16(3):203-222. doi: 10.1038/nrd.2016.246. Epub 2017 Feb 17.
In just over two decades since the discovery of the first microRNA (miRNA), the field of miRNA biology has expanded considerably. Insights into the roles of miRNAs in development and disease, particularly in cancer, have made miRNAs attractive tools and targets for novel therapeutic approaches. Functional studies have confirmed that miRNA dysregulation is causal in many cases of cancer, with miRNAs acting as tumour suppressors or oncogenes (oncomiRs), and miRNA mimics and molecules targeted at miRNAs (antimiRs) have shown promise in preclinical development. Several miRNA-targeted therapeutics have reached clinical development, including a mimic of the tumour suppressor miRNA miR-34, which reached phase I clinical trials for treating cancer, and antimiRs targeted at miR-122, which reached phase II trials for treating hepatitis. In this article, we describe recent advances in our understanding of miRNAs in cancer and in other diseases and provide an overview of current miRNA therapeutics in the clinic. We also discuss the challenge of identifying the most efficacious therapeutic candidates and provide a perspective on achieving safe and targeted delivery of miRNA therapeutics.
自第一个 microRNA(miRNA)被发现以来,仅仅二十多年的时间,miRNA 生物学领域已经得到了极大的扩展。miRNA 在发育和疾病(尤其是癌症)中的作用的深入了解,使得 miRNA 成为新型治疗方法的有吸引力的工具和靶点。功能研究已经证实,miRNA 失调在许多癌症病例中是因果关系,miRNA 可以作为肿瘤抑制因子或癌基因(oncomiRs),miRNA 模拟物和针对 miRNA 的分子(antimiRs)在临床前开发中显示出了希望。几种 miRNA 靶向治疗药物已经进入临床开发阶段,包括肿瘤抑制因子 miRNA miR-34 的模拟物,该模拟物已经进入治疗癌症的 I 期临床试验,以及针对 miR-122 的 antimiRs,已经进入治疗肝炎的 II 期临床试验。在本文中,我们描述了我们对癌症和其他疾病中 miRNA 的理解的最新进展,并对临床中当前的 miRNA 治疗方法进行了概述。我们还讨论了确定最有效的治疗候选物的挑战,并提供了实现 miRNA 治疗剂安全靶向递送的观点。