| Literature DB >> 33507586 |
Tingyu Zong1, Yanyan Yang2, Hui Zhao3, Lin Li4, Meixin Liu1, Xiuxiu Fu1, Guozhang Tang1, Hong Zhou1, Lynn Htet Htet Aung5, Peifeng Li5, Jianxun Wang2, Zhibin Wang1, Tao Yu1,5.
Abstract
tsRNAs are small fragments of RNAs with specific lengths that are generated by particular ribonucleases, such as dicer and angiogenin (ANG), clipping on the rings of transfer RNAs (tRNAs) in specific cells and tissues under specific conditions. Depending on where the splicing site is, tsRNAs can be segmented into two main types, tRNA-derived stress-induced RNAs (tiRNAs) and tRNA-derived fragments (tRFs). Many studies have shown that tsRNAs are functional molecules, not the random degradative products of tRNAs. Notably, due to their regulatory mechanism in regulating mRNA stability, transcription, ribosomal RNA (rRNA) synthesis and RNA reverse transcription, tsRNAs are significantly involved in the cell function, such as cell proliferation, migration, cycle and apoptosis, as well as the occurrence and development of a variety of diseases. In addition, tsRNAs may represent a new generation of clinical biomarkers or therapeutic targets because of their stable structures, high conservation and widely distribution, particularly in the peripheral tissues, bodily fluids and exosomes. In this review, we describe the generation, function and mechanism of tsRNAs and illustrate the current research progress of tsRNAs in various diseases, highlight their potentials as biomarkers and therapeutic targets in clinical application. Although our understanding of tsRNAs is still in infancy, the application prospects shown in this field deserve further exploration.Entities:
Keywords: biomarker; cell proliferation; clinical; tRNA-derived small RNAs; therapeutic target
Year: 2021 PMID: 33507586 DOI: 10.1111/cpr.12977
Source DB: PubMed Journal: Cell Prolif ISSN: 0960-7722 Impact factor: 6.831