Goleij Pouya, Babamohamadi Mehregan, Rezaee Aryan, Sanaye Pantea Majma, Tabari Mohammad Amin Khazeei, Sadreddini Sarvin, Arefnezhad Reza, Motedayyen Hossein
Department of Genetics, Sana Institute of Higher Education, Sari, Iran; USERN Office, Kermanshah University of Medical Sciences, Kermanshah, Iran.
USERN Office, Kermanshah University of Medical Sciences, Kermanshah, Iran; Department of Biology, School of Natural Sciences, University of Tabriz, Tabriz, Iran; Stem Cell and Regenerative Medicine Innovation Center, Tehran University of Medical Sciences, Tehran, Iran.
Prog Mol Biol Transl Sci. 2024;203:41-63. doi: 10.1016/bs.pmbts.2023.12.022. Epub 2024 Jan 25.
RNA therapy is one of the new treatments using small RNA molecules to target and regulate gene expression. It involves the application of synthetic or modified RNA molecules to inhibit the expression of disease-causing genes specifically. In other words, it silences genes and suppresses the transcription process. The main theory behind RNA therapy is that RNA molecules can prevent the translation into proteins by binding to specific messenger RNA (mRNA) molecules. By targeting disease-related mRNA molecules, RNA therapy can effectively silence or reduce the development of harmful proteins. There are different types of RNA molecules used in therapy, including small interfering RNAs (siRNAs), microRNAs (miRNAs), aptamer, ribozyme, and antisense oligonucleotides (ASOs). These molecules are designed to complement specific mRNA sequences, allowing them to bind and degrade the targeted mRNA or prevent its translation into protein. Nanotechnology is also highlighted to increase the efficacy of RNA-based drugs. In this chapter, while examining various methods of RNA therapy, we discuss the advantages and challenges of each.
RNA疗法是一种利用小RNA分子靶向和调节基因表达的新型治疗方法。它涉及应用合成或修饰的RNA分子来特异性抑制致病基因的表达。换句话说,它使基因沉默并抑制转录过程。RNA疗法背后的主要理论是RNA分子可以通过与特定的信使RNA(mRNA)分子结合来阻止其翻译成蛋白质。通过靶向与疾病相关的mRNA分子,RNA疗法可以有效地使有害蛋白质沉默或减少其产生。治疗中使用的RNA分子有不同类型,包括小干扰RNA(siRNA)、微小RNA(miRNA)、适体、核酶和反义寡核苷酸(ASO)。这些分子被设计成与特定的mRNA序列互补,使其能够结合并降解靶向的mRNA或阻止其翻译成蛋白质。纳米技术也被强调用于提高基于RNA的药物的疗效。在本章中,在研究RNA疗法的各种方法时,我们将讨论每种方法的优点和挑战。