TY - JOUR
T1 - Insights Into the Role of CircRNAs
T2 - Biogenesis, Characterization, Functional, and Clinical Impact in Human Malignancies
AU - Nisar, Sabah
AU - Bhat, Ajaz A.
AU - Singh, Mayank
AU - Karedath, Thasni
AU - Rizwan, Arshi
AU - Hashem, Sheema
AU - Bagga, Puneet
AU - Reddy, Ravinder
AU - Jamal, Farrukh
AU - Uddin, Shahab
AU - Chand, Gyan
AU - Bedognetti, Davide
AU - El-Rifai, Wael
AU - Frenneaux, Michael P.
AU - Macha, Muzafar A.
AU - Ahmed, Ikhlak
AU - Haris, Mohammad
N1 - Publisher Copyright:
© Copyright © 2021 Nisar, Bhat, Singh, Karedath, Rizwan, Hashem, Bagga, Reddy, Jamal, Uddin, Chand, Bedognetti, El-Rifai, Frenneaux, Macha, Ahmed and Haris.
PY - 2021/2/5
Y1 - 2021/2/5
N2 - Circular RNAs (circRNAs) are an evolutionarily conserved novel class of non-coding endogenous RNAs (ncRNAs) found in the eukaryotic transcriptome, originally believed to be aberrant RNA splicing by-products with decreased functionality. However, recent advances in high-throughput genomic technology have allowed circRNAs to be characterized in detail and revealed their role in controlling various biological and molecular processes, the most essential being gene regulation. Because of the structural stability, high expression, availability of microRNA (miRNA) binding sites and tissue-specific expression, circRNAs have become hot topic of research in RNA biology. Compared to the linear RNA, circRNAs are produced differentially by backsplicing exons or lariat introns from a pre-messenger RNA (mRNA) forming a covalently closed loop structure missing 3′ poly-(A) tail or 5′ cap, rendering them immune to exonuclease-mediated degradation. Emerging research has identified multifaceted roles of circRNAs as miRNA and RNA binding protein (RBP) sponges and transcription, translation, and splicing event regulators. CircRNAs have been involved in many human illnesses, including cancer and neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease, due to their aberrant expression in different pathological conditions. The functional versatility exhibited by circRNAs enables them to serve as potential diagnostic or predictive biomarkers for various diseases. This review discusses the properties, characterization, profiling, and the diverse molecular mechanisms of circRNAs and their use as potential therapeutic targets in different human malignancies.
AB - Circular RNAs (circRNAs) are an evolutionarily conserved novel class of non-coding endogenous RNAs (ncRNAs) found in the eukaryotic transcriptome, originally believed to be aberrant RNA splicing by-products with decreased functionality. However, recent advances in high-throughput genomic technology have allowed circRNAs to be characterized in detail and revealed their role in controlling various biological and molecular processes, the most essential being gene regulation. Because of the structural stability, high expression, availability of microRNA (miRNA) binding sites and tissue-specific expression, circRNAs have become hot topic of research in RNA biology. Compared to the linear RNA, circRNAs are produced differentially by backsplicing exons or lariat introns from a pre-messenger RNA (mRNA) forming a covalently closed loop structure missing 3′ poly-(A) tail or 5′ cap, rendering them immune to exonuclease-mediated degradation. Emerging research has identified multifaceted roles of circRNAs as miRNA and RNA binding protein (RBP) sponges and transcription, translation, and splicing event regulators. CircRNAs have been involved in many human illnesses, including cancer and neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease, due to their aberrant expression in different pathological conditions. The functional versatility exhibited by circRNAs enables them to serve as potential diagnostic or predictive biomarkers for various diseases. This review discusses the properties, characterization, profiling, and the diverse molecular mechanisms of circRNAs and their use as potential therapeutic targets in different human malignancies.
KW - RNA binding protein
KW - circRNA
KW - drug resistance
KW - miRNA sponges
KW - signaling pathways
KW - tumor
UR - http://www.scopus.com/inward/record.url?scp=85101209265&partnerID=8YFLogxK
U2 - 10.3389/fcell.2021.617281
DO - 10.3389/fcell.2021.617281
M3 - Review article
AN - SCOPUS:85101209265
SN - 2296-634X
VL - 9
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 617281
ER -