Sioud M
Institute for Cancer Research, Department of Immunology, The Norwegian Radium Hospital, Montebello, Oslo.
Curr Mol Med. 2001 Nov;1(5):575-88. doi: 10.2174/1566524013363366.
Recent molecular and cellular studies have highlighted the important role of some gene products in the cause and/or perpetuation of human pathological conditions including cancer and autoimmune diseases. The identification of such gene products has led to the development of new candidate therapies. The discovery of catalytic nucleic acid enzymes has provided researchers with a potentially important tool to block the expression of abnormal genes, provided that their sequences are known. The cleavage specificity of these compounds is determined by their hybridizing antisense arms, which anneal with the target mRNA in a complementary fashion. Nucleic acid enzymes can be delivered to cells either endogenously as gene encoding RNA enzymes (ribozymes) or exogenously as in vitro made agents. Given the progress reported during the last years, a wide range of molecular designs and chemical modifications can be introduced into these compounds, in particular the hammerhead type ribozyme. Here, we review the design, stability and the therapeutic application of these agents with the goals of illustrating relevant gene targets and signal pathways for molecular medicine. Relevant in vivo problems of the technology, mRNA repair by group I intron ribozymes and gene regulation by endogenous RNA will also be discussed.
最近的分子和细胞研究突出了某些基因产物在包括癌症和自身免疫性疾病在内的人类病理状况的起因和/或持续存在过程中的重要作用。此类基因产物的鉴定推动了新候选疗法的开发。催化核酸酶的发现为研究人员提供了一种潜在的重要工具,用于阻断异常基因的表达,前提是其序列已知。这些化合物的切割特异性由其杂交反义臂决定,反义臂以互补方式与靶mRNA退火。核酸酶可以作为编码RNA酶的基因(核酶)内源性地递送至细胞,也可以作为体外制备的试剂外源性地递送至细胞。鉴于过去几年所报道的进展,可以将多种分子设计和化学修饰引入这些化合物,尤其是锤头型核酶。在此,我们综述这些试剂的设计、稳定性及治疗应用,目的是阐明分子医学相关的基因靶点和信号通路。还将讨论该技术在体内的相关问题以及I组内含子核酶对mRNA的修复和内源性RNA对基因的调控。