Inter-institutional Grad Program in Bioinformatics, University of Sao Paulo, Sao Paulo, SP, Brazil.
Inter-institutional Grad Program in Bioinformatics, University of Sao Paulo, Sao Paulo, SP, Brazil.
Comput Biol Chem. 2022 Oct;100:107729. doi: 10.1016/j.compbiolchem.2022.107729. Epub 2022 Jul 12.
MicroRNAs (miRNAs) are non-coding RNAs containing 19-26 nucleotides, and they directly regulate the translation of mRNAs by binding to them. MiRNAs participate in various physiological processes and are associated with the development of diseases, such as cancer. Therefore, understanding miRNAs regulation on targets is crucial for understanding the mechanisms of diseases and for obtaining a more suitable treatment. In animals, the base complementarity between miRNAs and the mRNA is imperfect, hindering the prediction of these targets. Thus, over the past 15 years, several computational tools have emerged for the prediction of miRNA targets in animals, generally with a focus on human expression data. Taking into account the wide range of prediction tools, a systematic review is presented here to analyze and classify these methods and features to enable the most appropriate choice according to the needs of each researcher. In this study, only articles whose methods met the inclusion and exclusion criteria established in the protocol were considered. The search was performed in November 2020, in two search engines PubMed and VHL Regional Portal. Among the initial 5315 journals found in the two searches, 78 articles were accepted, comprising 49 different tools analyzed and grouped by features and method similarities. As we limited our criteria to animals, all tools found in our search were suitable for human studies. The results demonstrated the evolution of prediction tools, including the most used features, such as alignment and thermodynamics, the methods used, as well as performance issues. It is possible to conclude that the currently available miRNA target prediction tools and methods can be aggregated with new features or other methods to improve accuracy.
微小 RNA(miRNAs)是含有 19-26 个核苷酸的非编码 RNA,通过与它们结合直接调节 mRNAs 的翻译。miRNAs 参与各种生理过程,并与疾病的发展有关,如癌症。因此,了解 miRNAs 对靶标的调控对于理解疾病的机制和获得更合适的治疗方法至关重要。在动物中,miRNAs 和 mRNA 之间的碱基互补不完全,这阻碍了这些靶标的预测。因此,在过去的 15 年中,已经出现了几种用于预测动物中 miRNA 靶标的计算工具,通常侧重于人类表达数据。考虑到广泛的预测工具,本文进行了系统综述,以分析和分类这些方法和特征,以便根据每个研究人员的需求进行最合适的选择。在这项研究中,仅考虑了其方法符合方案中建立的纳入和排除标准的文章。搜索于 2020 年 11 月在两个搜索引擎 PubMed 和 VHL Regional Portal 中进行。在两次搜索中最初找到的 5315 种期刊中,有 78 篇文章被接受,其中包括 49 种不同的工具,根据特征和方法的相似性进行了分析和分组。由于我们将标准限于动物,因此我们在搜索中发现的所有工具都适用于人类研究。结果表明了预测工具的发展,包括最常用的特征,如比对和热力学,以及使用的方法和性能问题。可以得出结论,目前可用的 miRNA 靶标预测工具和方法可以与新的特征或其他方法结合使用,以提高准确性。