Wang Haicun, Gao Xin, Yu Shaobo, Wang Weina, Liu Guanglin, Jiang Xingming, Sun Dongsheng
General Surgery Department, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, China.
Department of Anesthesiology, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, China.
Front Oncol. 2022 Aug 25;12:947775. doi: 10.3389/fonc.2022.947775. eCollection 2022.
CircRNAs have been the focus of research in recent years. They are differentially expressed in various human tumors and can regulate oncogenes and tumor suppressor genes expression through various mechanisms. The diversity, stability, evolutionary conservatism and cell- or tissue-specific expression patterns of circRNAs also endow them with important regulatory roles in promoting or inhibiting tumor cells malignant biological behaviors progression. More interestingly, emerging studies also found that circRNAs can regulate not only other genes expression, but also their parental gene expression and thus influence tumors development. Apart from some conventional features, circRNAs have a certain specificity in the regulation of parental gene expression, with a higher proportion affecting parental gene transcription and easier translation into protein to regulate parental gene expression. CircRNAs are generally thought to be unable to produce proteins and therefore the protein-coding ability exhibited by circRNAs in regulating parental gene expression is unique and indicates that the regulatory effects of parental gene expression by circRNAs are not only a competitive binding relationship, but also a more complex molecular relationship between circRNAs and parental gene, which deserves further study. This review summarizes the molecular mechanisms of circRNAs regulating parental gene expression and their biological roles in tumorigenesis and development, aiming to provide new ideas for the clinical application of circRNAs in tumor-targeted therapy.
环状RNA(circRNAs)近年来一直是研究的热点。它们在各种人类肿瘤中差异表达,并可通过多种机制调节癌基因和肿瘤抑制基因的表达。circRNAs的多样性、稳定性、进化保守性以及细胞或组织特异性表达模式,也赋予了它们在促进或抑制肿瘤细胞恶性生物学行为进展方面的重要调控作用。更有趣的是,新兴研究还发现circRNAs不仅可以调节其他基因的表达,还可以调节其亲本基因的表达,从而影响肿瘤的发展。除了一些常规特征外,circRNAs在亲本基因表达调控方面具有一定的特异性,影响亲本基因转录的比例较高,且更容易翻译成蛋白质来调控亲本基因表达。一般认为circRNAs不能产生蛋白质,因此circRNAs在调控亲本基因表达时所表现出的蛋白质编码能力是独特的,这表明circRNAs对亲本基因表达的调控作用不仅是一种竞争性结合关系,而且是circRNAs与亲本基因之间更复杂的分子关系,值得进一步研究。本综述总结了circRNAs调控亲本基因表达的分子机制及其在肿瘤发生发展中的生物学作用,旨在为circRNAs在肿瘤靶向治疗中的临床应用提供新思路。