Wacheck Volker
Abteilung für Experimentelle Onkologie/Molekulare Pharmakologie, Universitätsklinik für Klinische Pharmakologie, Medizinische Universität Wien, Wien, Austria.
Wien Med Wochenschr. 2006 Sep;156(17-18):481-7. doi: 10.1007/s10354-006-0331-4.
Oligonucleotide therapeutics are short, single- or double-stranded DNA or RNA molecules consisting of strands of 10-50 nucleotides. By targeted modulation of gene expression oligonucleotides provide the chance of targeting diseases at their molecular level. Within this novel emerging class of compounds oligonucleotide therapeutics are discriminated by their structure, function and mode of action. While antisense oligonucleotides, ribozymes and siRNAs suppress the expression of a protein by complementary hybridizing with their target mRNA, aptamers bind like antibodies to their target protein and thereby inhibit its function. Immunostimulatory oligonucleotides are due to sequence motifs within their nucleotide sequence able to trigger a therapeutic exploitable immune response. Currently, there are only two oligonucleotide therapeutics approved by the FDA, namely the antisense oligonucleotide Fomivirsen and the aptamer Macugen. In this review the mode of action of the diverse oligonucleotide therapeutics and their current status in clinical development will be discussed.
寡核苷酸疗法是由10至50个核苷酸链组成的短单链或双链DNA或RNA分子。通过对基因表达的靶向调节,寡核苷酸提供了在分子水平上针对疾病的机会。在这类新兴的化合物中,寡核苷酸疗法根据其结构、功能和作用方式进行区分。反义寡核苷酸、核酶和小干扰RNA通过与其靶mRNA互补杂交来抑制蛋白质的表达,而适体则像抗体一样与其靶蛋白结合,从而抑制其功能。免疫刺激寡核苷酸由于其核苷酸序列中的序列基序能够引发可用于治疗的免疫反应。目前,美国食品药品监督管理局(FDA)仅批准了两种寡核苷酸疗法,即反义寡核苷酸福米韦生和适体麦考酚酯。在本综述中,将讨论各种寡核苷酸疗法的作用方式及其在临床开发中的现状。