Heidenreich O, Kang S H, Xu X, Nerenberg M
Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037, USA.
Mol Med Today. 1995 Jun;1(3):128-33. doi: 10.1016/s1357-4310(95)80090-5.
Antisense oligonucleotides inhibit gene expression by binding in a sequence-specific manner to an RNA target. Modern nucleotide chemistry has enabled the synthesis of chemically modified oligonucleotides that are highly resistant to nuclease degradation. Among other applications, these agents are currently being evaluated as potential antiviral and anticancer drugs. However, several unsolved problems remain. Poor efficiency of delivery to cells, tissue toxicity and antisense-independent biological effects of oligonucleotides currently limit the widespread application of antisense oligonucleotides to human disease. This article reviews some of the applications of antisense oligonucleotides and discusses problems associated with these applications.
反义寡核苷酸通过以序列特异性方式与RNA靶标结合来抑制基因表达。现代核苷酸化学技术已能够合成对核酸酶降解具有高度抗性的化学修饰寡核苷酸。在其他应用中,这些药物目前正在作为潜在的抗病毒和抗癌药物进行评估。然而,仍存在一些未解决的问题。目前,寡核苷酸向细胞的递送效率低下、组织毒性以及与反义无关的生物学效应限制了反义寡核苷酸在人类疾病中的广泛应用。本文综述了反义寡核苷酸的一些应用,并讨论了与这些应用相关的问题。