Rad Seyed Mohammad Ali Hosseini, Langroudi Lida, Kouhkan Fatemeh, Yazdani Laleh, Koupaee Alireza Nouri, Asgharpour Sara, Shojaei Zahra, Bamdad Taravat, Arefian Ehsan
Department of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, 1997775555, Tehran, Iran,
Tumour Biol. 2015 Jul;36(7):4871-81. doi: 10.1007/s13277-015-3344-z. Epub 2015 Apr 4.
Gene therapy as a therapeutic approach has been the dream for many scientists around the globe. Many strategies have been proposed and applied for this purpose, yet the void for a functional safe method is still apparent. Since most of the diseases are caused by undesirable upregulation (oncogenes) or downregulation (tumor suppressor genes) of genes, major gene therapy's techniques affect gene expression. Most of the methods are used in post-transcriptional level such as RNA inhibitory (RNAi) and splice-switching oligonucleotides (SSOs). RNAi blocks messenger RNA (mRNA) translation by mRNA degradation or interruption between attachments of mRNA with ribosomes' subunits. However, one of the novel methods is the usage of transcription factor targeted decoys. DNA decoys are the new generation of functional gene downregulatory oligonucleotides which compete with specific binding sites of transcription factors. Considering the exponential growth of this technique in both in vitro and in vivo studies, in this paper, we aim to line out the description, design, and application of decoys in research and therapy.
基因治疗作为一种治疗方法,一直是全球众多科学家的梦想。为此人们提出并应用了许多策略,但仍明显缺乏一种有效的安全方法。由于大多数疾病是由基因的不良上调(癌基因)或下调(肿瘤抑制基因)引起的,主要的基因治疗技术会影响基因表达。大多数方法用于转录后水平,如RNA干扰(RNAi)和剪接转换寡核苷酸(SSO)。RNAi通过mRNA降解或mRNA与核糖体亚基结合之间的中断来阻断信使RNA(mRNA)翻译。然而,一种新方法是使用靶向转录因子的诱饵。DNA诱饵是新一代功能性基因下调寡核苷酸,可与转录因子的特定结合位点竞争。鉴于该技术在体外和体内研究中的指数增长,在本文中,我们旨在阐述诱饵在研究和治疗中的描述、设计及应用。