Keio Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Innovation Center of NanoMedicine, Kawasaki Institute of Industrial Promotion, Kawasaki, Japan.
Cancer Sci. 2022 Sep;113(9):2952-2961. doi: 10.1111/cas.15461. Epub 2022 Jul 11.
Oligonucleotide therapeutics, drugs consisting of 10-50 nucleotide-long single- or double-stranded DNA or RNA molecules that can bind to specific DNA or RNA sequences or proteins, include antisense oligonucleotides (ASOs), small interfering RNAs (siRNAs), microRNAs (miRNAs), aptamers, and decoys. These oligonucleotide therapeutics could potentially become the third pillar of drug development. In particular, ASOs and siRNAs are advanced tools that are widely used to silence gene expression. They are used in clinical trials, as they have high specificity for target mRNAs and non-coding RNAs and limited toxicity. However, their clinical application remains challenging. Although chemotherapy has benefits, it has severe adverse effects in many patients. Therefore, new modalities for targeted molecular therapy against tumors, including oligonucleotide therapeutics, are required, and they should be compatible with diagnosis using next-generation sequencing. This review provides an overview of the therapeutic uses of ASOs, siRNAs, and miRNAs in clinical studies on malignant tumors. Understanding previous research and development will help in developing novel oligonucleotide therapeutics against malignant tumors.
寡核苷酸疗法是一种由 10-50 个核苷酸组成的单链或双链 DNA 或 RNA 分子药物,能够与特定的 DNA 或 RNA 序列或蛋白质结合,包括反义寡核苷酸(ASO)、小干扰 RNA(siRNA)、微小 RNA(miRNA)、适体和诱饵。这些寡核苷酸疗法有可能成为药物开发的第三大支柱。特别是 ASO 和 siRNA 是广泛用于沉默基因表达的先进工具。它们被用于临床试验,因为它们对靶 mRNA 和非编码 RNA 具有高度特异性,并且毒性有限。然而,它们的临床应用仍然具有挑战性。虽然化疗有好处,但它在许多患者中会产生严重的不良反应。因此,需要针对肿瘤的靶向分子治疗的新方法,包括寡核苷酸疗法,并且它们应该与使用下一代测序进行的诊断兼容。本综述概述了 ASO、siRNA 和 miRNA 在恶性肿瘤临床研究中的治疗用途。了解以前的研究和开发将有助于开发针对恶性肿瘤的新型寡核苷酸疗法。