Institute of Biosciences and BioResources-UOS Naples CNR, via P. Castellino, 111-80131, Naples, Italy.
IRCCS Neuromed, Pozzilli, IS, Italy.
J Exp Clin Cancer Res. 2021 Dec 4;40(1):383. doi: 10.1186/s13046-021-02193-1.
Short or small interfering RNAs (siRNAs) and microRNA (miRNAs) are molecules similar in size and function able to inhibit gene expression based on their complementarity with mRNA sequences, inducing the degradation of the transcript or the inhibition of their translation.siRNAs bind specifically to a single gene location by sequence complementarity and regulate gene expression by specifically targeting transcription units via posttranscriptional gene silencing. miRNAs can regulate the expression of different gene targets through their imperfect base pairing.This process - known as RNA interference (RNAi) - modulates transcription in order to maintain a correct physiological environment, playing a role in almost the totality of the cellular pathways.siRNAs have been evolutionary evolved for the protection of genome integrity in response to exogenous and invasive nucleic acids such as transgenes or transposons. Artificial siRNAs are widely used in molecular biology for transient silencing of genes of interest. This strategy allows to inhibit the expression of any target protein of known sequence and is currently used for the treatment of different human diseases including cancer.Modifications and rearrangements in gene regions encoding for miRNAs have been found in cancer cells, and specific miRNA expression profiles characterize the developmental lineage and the differentiation state of the tumor. miRNAs with different expression patterns in tumors have been reported as oncogenes (oncomirs) or tumor-suppressors (anti-oncomirs). RNA modulation has become important in cancer research not only for development of early and easy diagnosis tools but also as a promising novel therapeutic approach.Despite the emerging discoveries supporting the role of miRNAs in carcinogenesis and their and siRNAs possible use in therapy, a series of concerns regarding their development, delivery and side effects have arisen.In this review we report the biology of miRNAs and siRNAs in relation to cancer summarizing the recent methods described to use them as novel therapeutic drugs and methods to specifically deliver them to cancer cells and overcome the limitations in the use of these molecules.
短链或小干扰 RNA(siRNA)和 microRNA(miRNA)是大小和功能相似的分子,能够基于与 mRNA 序列的互补性抑制基因表达,诱导转录本降解或翻译抑制。siRNA 通过序列互补特异性结合到单个基因位置,并通过转录后基因沉默特异性靶向转录单元来调节基因表达。miRNA 可以通过不完全碱基配对调节不同基因靶标的表达。这种过程 - 称为 RNA 干扰(RNAi)- 调节转录以维持正确的生理环境,在几乎所有细胞途径中都发挥作用。siRNA 是为了保护基因组完整性而进化的,以应对外源和入侵的核酸,如转基因或转座子。人工 siRNA 在分子生物学中被广泛用于瞬时沉默感兴趣的基因。这种策略允许抑制任何已知序列的靶蛋白的表达,目前用于治疗包括癌症在内的不同人类疾病。在癌细胞中发现了编码 miRNA 的基因区域的修饰和重排,并且特定的 miRNA 表达谱特征化了肿瘤的发育谱系和分化状态。在肿瘤中具有不同表达模式的 miRNAs 被报道为癌基因(oncomirs)或肿瘤抑制因子(anti-oncomirs)。RNA 调节在癌症研究中变得重要,不仅是为了开发早期和易于诊断的工具,而且还作为一种有前途的新型治疗方法。尽管新兴的发现支持 miRNA 在致癌作用中的作用及其在治疗中的可能用途,但对它们的开发、递送和副作用的一系列担忧已经出现。在这篇综述中,我们报告了 miRNA 和 siRNA 在癌症中的生物学,总结了最近描述的将它们用作新型治疗药物的方法以及将它们特异性递送到癌细胞的方法,并克服了这些分子使用中的局限性。