CircNet 2.0: an updated database for exploring circular RNA regulatory networks in cancers

Yi-Gang Chen(Shenzhen Maternity and Child Healthcare Hospital), Lantian Yao(Chinese University of Hong Kong, Shenzhen), Yun Tang(Chinese University of Hong Kong, Shenzhen), Jhih-Hua Jhong(Chinese University of Hong Kong, Shenzhen), Jingting Wan(Chinese University of Hong Kong, Shenzhen), Jingyue Chang(Chinese University of Hong Kong, Shenzhen), Shidong Cui(Chinese University of Hong Kong, Shenzhen), Yijun Luo(Chinese University of Hong Kong, Shenzhen), Xiaoxuan Cai(Chinese University of Hong Kong, Shenzhen), Wenshuo Li(Chinese University of Hong Kong, Shenzhen), Qi Chen(Chinese University of Hong Kong, Shenzhen), Hsi‐Yuan Huang(Shenzhen Maternity and Child Healthcare Hospital), Zhuo Wang(Chinese University of Hong Kong, Shenzhen), Wei‐Ming Chen(Chinese University of Hong Kong, Shenzhen), Tzu‐Hao Chang(Taipei Medical University), Fengxiang Wei(Jiamusi University), Tzong-Yi Lee(Chinese University of Hong Kong, Shenzhen), Hsien‐Da Huang(Shenzhen Maternity and Child Healthcare Hospital)
Nucleic Acids Research
October 25, 2021
Cited by 76Open Access
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Abstract

Circular RNAs (circRNAs), which are single-stranded RNA molecules that have individually formed into a covalently closed continuous loop, act as sponges of microRNAs to regulate transcription and translation. CircRNAs are important molecules in the field of cancer diagnosis, as growing evidence suggests that they are closely related to pathological cancer features. Therefore, they have high potential for clinical use as novel cancer biomarkers. In this article, we present our updates to CircNet (version 2.0), into which circRNAs from circAtlas and MiOncoCirc, and novel circRNAs from The Cancer Genome Atlas database have been integrated. In total, 2732 samples from 37 types of cancers were integrated into CircNet 2.0 and analyzed using several of the most reliable circRNA detection algorithms. Furthermore, target miRNAs were predicted from the full-length circRNA sequence using three reliable tools (PITA, miRanda and TargetScan). Additionally, 384 897 experimentally verified miRNA-target interactions from miRTarBase were integrated into our database to facilitate the construction of high-quality circRNA-miRNA-gene regulatory networks. These improvements, along with the user-friendly interactive web interface for data presentation, search, and visualization, showcase the updated CircNet database as a powerful, experimentally validated resource, for providing strong data support in the biomedical fields. CircNet 2.0 is currently accessible at https://awi.cuhk.edu.cn/∼CircNet.


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