Circular RNA and its mechanisms in disease: From the bench to the clinic

被引:667
作者
Han, Bing [1 ]
Chao, Jie [2 ]
Yao, Honghong [1 ,3 ]
机构
[1] Southeast Univ, Sch Med, Dept Pharmacol, Nanjing, Jiangsu, Peoples R China
[2] Southeast Univ, Sch Med, Dept Physiol, Nanjing, Jiangsu, Peoples R China
[3] Southeast Univ, Key Lab Dev Genes & Human Dis, Inst Life Sci, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
circRNAs; Biogenesis; Function; Disease; Biomarker; Therapeutic target; MICROARRAY EXPRESSION PROFILE; PROMOTES CELL-PROLIFERATION; AMYLOID PRECURSOR PROTEIN; LONG NONCODING RNAS; MESSENGER-RNA; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; COLORECTAL-CANCER; REGULATORY ROLE; EMERGING ROLES;
D O I
10.1016/j.pharmthera.2018.01.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The emerging recognition of the functional roles of circular RNAs (circRNAs) has given rise to a new perspective regarding our understanding of cellular physiology and disease pathogenesis. Unlike linear RNAs, circRNAs are covalently closed continuous loops that act as gene regulators in mammals, and their sequence composition determines the mode of circRNA biogenesis. The availability and integrated use of advanced genome analysis platforms have allowed the identification of a large number of these molecules. Their high abundance, stability and evolutionary conservation among species endow circRNAs with numerous potential functions, such as acting as microRNA (miRNA) sponges or binding to RNA-associated proteins to form RNA-protein complexes that regulate gene transcription. Moreover, circRNAs have been shown to be expressed in a tissue-specific manner and in pathological conditions, which has stimulated significant interest in their role in human disease and cancer. In this concise review, we outline the characteristics, functions and mechanisms of action of circRNAs as well as their involvement in different diseases. Although their exact roles and mechanisms of gene regulation remain to be clarified, circRNAs have potential applications as disease biomarkers and novel therapeutic targets. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 44
页数:14
相关论文
共 193 条
[1]   Identification of HuR target circular RNAs uncovers suppression of PABPN1 translation by CircPABPN1 [J].
Abdelmohsen, Kotb ;
Panda, Amaresh C. ;
Munk, Rachel ;
Grammatikakis, Ioannis ;
Dudekula, Dawood B. ;
De, Supriyo ;
Kim, Jiyoung ;
Noh, Ji Heon ;
Kim, Kyoung Mi ;
Martindale, Jennifer L. ;
Gorospe, Myriam .
RNA BIOLOGY, 2017, 14 (03) :361-369
[2]   Rolling Circle Translation of Circular RNA in Living Human Cells [J].
Abe, Naoko ;
Matsumoto, Ken ;
Nishihara, Mizuki ;
Nakano, Yukiko ;
Shibata, Aya ;
Maruyama, Hideto ;
Shuto, Satoshi ;
Matsuda, Akira ;
Yoshida, Minoru ;
Ito, Yoshihiro ;
Abe, Hiroshi .
SCIENTIFIC REPORTS, 2015, 5
[3]   Annotating non-coding regions of the genome [J].
Alexander, Roger P. ;
Fang, Gang ;
Rozowsky, Joel ;
Snyder, Michael ;
Gerstein, Mark B. .
NATURE REVIEWS GENETICS, 2010, 11 (08) :559-571
[4]   miARma-Seq: a comprehensive tool for miRNA, mRNA and circRNA analysis [J].
Andres-Leon, Eduardo ;
Nunez-Torres, Rocio ;
Rojas, Ana M. .
SCIENTIFIC REPORTS, 2016, 6
[5]  
[Anonymous], RNA BIOL
[6]  
[Anonymous], AUTOPHAGY
[7]  
[Anonymous], BIOMED RES INT
[8]   circRNA Biogenesis Competes with Pre-mRNA Splicing [J].
Ashwal-Fluss, Reut ;
Meyer, Markus ;
Pamudurti, Nagarjuna Reddy ;
Ivanov, Andranik ;
Bartok, Osnat ;
Hanan, Mor ;
Evantal, Naveh ;
Memczak, Sebastian ;
Rajewsky, Nikolaus ;
Kadener, Sebastian .
MOLECULAR CELL, 2014, 56 (01) :55-66
[9]   Correlation of circular RNA abundance with proliferation - exemplified with colorectal and ovarian cancer, idiopathic lung fibrosis, and normal human tissues [J].
Bachmayr-Heyda, Anna ;
Reiner, Agnes T. ;
Auer, Katharina ;
Sukhbaatar, Nyamdelger ;
Aust, Stefanie ;
Bachleitner-Hofmann, Thomas ;
Mesteri, Ildiko ;
Grunt, Thomas W. ;
Zeillinger, Robert ;
Pils, Dietmar .
SCIENTIFIC REPORTS, 2015, 5 :8057
[10]   The Landscape of MicroRNA, Piwi-Interacting RNA, and Circular RNA in Human Saliva [J].
Bahn, Jae Hoon ;
Zhang, Qing ;
Li, Feng ;
Chan, Tak-Ming ;
Lin, Xianzhi ;
Kim, Yong ;
Wong, David T. W. ;
Xiao, Xinshu .
CLINICAL CHEMISTRY, 2015, 61 (01) :221-230