Analysis of differentially expressed circular RNAs for the identification of a coexpression RNA network and signature in colorectal cancer.
Adult
Aged
Biomarkers, Tumor
/ genetics
Colorectal Neoplasms
/ genetics
Computational Biology
Female
Follow-Up Studies
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Gene Regulatory Networks
Humans
Lymphatic Metastasis
Male
MicroRNAs
/ genetics
Middle Aged
RNA, Circular
/ genetics
RNA, Messenger
/ genetics
RNA sequencing (RNA-seq)
circular RNA (circRNA)
circular RNA-messenger RNA (circRNA-mRNA) network
colorectal cancer (CRC)
Journal
Journal of cellular biochemistry
ISSN: 1097-4644
Titre abrégé: J Cell Biochem
Pays: United States
ID NLM: 8205768
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
10
09
2018
accepted:
27
09
2018
pubmed:
16
10
2018
medline:
10
7
2020
entrez:
16
10
2018
Statut:
ppublish
Résumé
Circular RNAs (circRNAs) play an important regulatory role in tumorigenesis. The aim of the present study was to analyze the circRNA expression network and elucidate its potential implications in colorectal cancer (CRC). The circRNA expression profile was analyzed in CRC tissues by RNA sequencing, and the functions of differentially expressed genes were analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. The circRNA network was predicted with bioinformatics. On the basis of the results, we identified 23 differentially expressed circRNAs in CRC; GO and KEGG analyses demonstrated that the changes in circRNAs were mainly associated with regulation of biological and metabolic processes through binding to other molecules. In addition, based on the predicted coexpression network, we identified a hub circRNA, hsa_circ_0009022. Subsequently, the results of sequencing were confirmed by reverse transcription-quantitative polymerase chain reaction, and hsa_circ_0000826 was found to be downregulated in CRC. Taken together, these findings indicate a set of differentially expressed circRNAs that may serve as a candidate diagnostic biomarker and a promising therapeutic target in CRC.
Substances chimiques
Biomarkers, Tumor
0
MicroRNAs
0
RNA, Circular
0
RNA, Messenger
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
6409-6419Informations de copyright
© 2018 Wiley Periodicals, Inc.