Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Domzale, Slovenia.
Cancer J. 2012 May-Jun;18(3):223-31. doi: 10.1097/PPO.0b013e318258b771.
MicroRNAs (miRNAs) are a class of noncoding RNAs (ncRNAs) and posttranscriptional gene regulators shown to be involved in pathogenesis of all types of human cancers. Their aberrant expression as tumor suppressors can lead to cancerogenesis by inhibiting malignant potential, or when acting as oncogenes, by activating malignant potential. Differential expression of miRNA genes in tumorous tissues can occur owing to several factors including positional effects when mapping to cancer-associated genomic regions, epigenetic mechanisms, and malfunctioning of the miRNA processing machinery, all of which can contribute to a complex miRNA-mediated gene network misregulation. They may increase or decrease expression of protein-coding genes, can target 3'-UTR or other genic regions (5'-UTR, promoter, coding sequences), and can function in various subcellular compartments, developmental, and metabolic processes. Because expanding research on miRNA-cancer associations has already produced large amounts of data, our main objective here was to summarize main findings and critically examine the intricate network connecting the miRNAs and coding genes in regulatory mechanisms and their function and phenotypic consequences for cancer. By examining such interactions, we aimed to gain insights for the development of new diagnostic markers as well as identification of potential venues for more selective tumor therapy. To enable efficient examination of the main past and current miRNA discoveries, we developed a Web-based miRNA timeline tool that will be regularly updated (http://www.integratomics-time.com/miRNA_timeline). Further development of this tool will be directed at providing additional analyses to clarify complex network interactions between miRNAs, other classes of ncRNAs, and protein-coding genes and their involvement in development of diseases including cancer. This tool therefore provides curated relevant information about the miRNA basic research and therapeutic application all at hand on one site to help researchers and clinicians in making informed decision about their miRNA cancer-related research or clinical practice.
MicroRNAs (miRNAs) 是一类非编码 RNA (ncRNA),作为转录后基因调控因子,参与所有类型人类癌症的发病机制。它们作为肿瘤抑制因子的异常表达可以通过抑制恶性潜能导致癌变,或者作为癌基因,通过激活恶性潜能导致癌变。由于多种因素,包括在癌症相关基因组区域定位时的位置效应、表观遗传机制以及 miRNA 加工机制的故障,肿瘤组织中 miRNA 基因的差异表达可能发生。它们可以增加或减少蛋白质编码基因的表达,可以靶向 3'-UTR 或其他基因区域(5'-UTR、启动子、编码序列),并且可以在各种亚细胞区室、发育和代谢过程中发挥作用。由于对 miRNA-癌症关联的扩展研究已经产生了大量数据,我们的主要目标是总结主要发现,并批判性地研究连接 miRNA 和编码基因的复杂调控网络及其在癌症中的功能和表型后果。通过研究这些相互作用,我们旨在为开发新的诊断标志物以及确定潜在的更具选择性的肿瘤治疗途径提供见解。为了能够有效地检查过去和当前 miRNA 的主要发现,我们开发了一个基于网络的 miRNA 时间线工具,该工具将定期更新(http://www.integratomics-time.com/miRNA_timeline)。进一步开发该工具将旨在提供额外的分析,以阐明 miRNA 与其他类别的 ncRNA 和蛋白质编码基因之间的复杂网络相互作用及其在包括癌症在内的疾病发展中的参与。因此,该工具在一个网站上提供了有关 miRNA 基础研究和治疗应用的精选相关信息,以帮助研究人员和临床医生在进行 miRNA 癌症相关研究或临床实践时做出明智的决策。