Doxakis Epaminondas
Center of Basic Research, Biomedical Research Foundation, Academy of Athens, 11527, Athens, Greece.
NPJ Parkinsons Dis. 2022 Jan 10;8(1):7. doi: 10.1038/s41531-021-00265-9.
Parkinson's disease (PD) is a complex, age-related, neurodegenerative disease whose etiology, pathology, and clinical manifestations remain incompletely understood. As a result, care focuses primarily on symptoms relief. Circular RNAs (circRNAs) are a large class of mostly noncoding RNAs that accumulate with aging in the brain and are increasingly shown to regulate all aspects of neuronal and glial development and function. They are generated by the spliceosome through the backsplicing of linear RNA. Although their biological role remains largely unknown, they have been shown to regulate transcription and splicing, act as decoys for microRNAs and RNA binding proteins, used as templates for translation, and serve as scaffolding platforms for signaling components. Considering that they are stable, diverse, and detectable in easily accessible biofluids, they are deemed promising biomarkers for diagnosing diseases. CircRNAs are differentially expressed in the brain of patients with PD, and growing evidence suggests that they regulate PD pathogenetic processes. Here, the biogenesis, expression, degradation, and detection of circRNAs, as well as their proposed functions, are reviewed. Thereafter, research linking circRNAs to PD-related processes, including aging, alpha-synuclein dysregulation, neuroinflammation, and oxidative stress is highlighted, followed by recent evidence for their use as prognostic and diagnostic biomarkers for PD.
帕金森病(PD)是一种复杂的、与年龄相关的神经退行性疾病,其病因、病理和临床表现仍未完全明确。因此,治疗主要侧重于缓解症状。环状RNA(circRNA)是一大类主要的非编码RNA,在大脑中会随着年龄增长而积累,并且越来越多地显示出对神经元和神经胶质细胞发育及功能的各个方面具有调节作用。它们由剪接体通过线性RNA的反向剪接产生。尽管它们的生物学作用在很大程度上仍不清楚,但已表明它们可调节转录和剪接,充当微小RNA和RNA结合蛋白的诱饵,用作翻译模板,并作为信号成分的支架平台。鉴于它们稳定且多样,并且在易于获取的生物流体中可检测到,它们被认为是诊断疾病的有前景的生物标志物。circRNA在PD患者的大脑中差异表达,越来越多的证据表明它们调节PD的发病过程。在此,对circRNA的生物合成、表达、降解和检测及其假定功能进行综述。此后,重点介绍了将circRNA与PD相关过程联系起来的研究,包括衰老、α-突触核蛋白失调、神经炎症和氧化应激,随后是它们用作PD预后和诊断生物标志物的最新证据。