Profiles of differentially expressed circRNAs in esophageal and breast cancer
Received 11 March 2018
Accepted for publication 7 May 2018
Published 23 July 2018 Volume 2018:10 Pages 2207—2221
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Editor who approved publication: Professor Lu-Zhe Sun
Peiyi Shi,1,* Jian Sun,2,* Biyu He,1 Huan Song,1 Zhongqi Li,1 Weimin Kong,2 Jianping Wang,3 Jianming Wang,1 Hengchuan Xue3
1Department of Epidemiology, School of Public Health, Nanjing Medical University, Nanjing, People’s Republic of China; 2Department of Thoracic Surgery, The First People’s Hospital of Yancheng City, Yancheng, People’s Republic of China; 3Department of Thoracic Surgery, People’s Hospital of Yangzhong, Yangzhong, People’s Republic of China
*These authors contributed equally to this work
Introduction: Circular RNAs (circRNAs) function as efficient microRNA sponges with gene-regulatory potential and are promising cancer biomarkers. In this study, we used the Arraystar Human circRNA Array to construct a genome-wide circRNA profile of esophageal squamous cell cancer (ESCC) and breast cancer (BC).
Patients and methods: Expression levels between cancer lesions and adjacent normal-appearing tissues were compared. We observed 469 upregulated circRNAs and 275 downregulated circRNAs in ESCC. Hsa_circRNA_103670 was upregulated 20.3-fold, while hsa_circRNA_030162 was downregulated 12.1-fold. For BC, 715 circRNAs were upregulated, and 440 circRNAs were downregulated. Hsa_circRNA_005230 was upregulated 12.2-fold, while hsa_circRNA_406225 was downregulated 12.4-fold.
Results: When we set the criteria as fold change in expression ≥2 between cancer and adjacent normal-appearing tissue with a P-value <0.01, there were 22 common circRNAs (11 upregulated and 11 downregulated) in relation to both ESCC and BC. Gene ontology and the Kyoto encyclopedia of genes and genomes analyses showed that these circRNAs were involved in the tumorigenesis of human cancers.
Conclusion: Our study revealed that circRNAs are promising candidates as valuable biomarkers for ESCC and BC, although relevant research is still in its infancy and the functional role of specific circRNAs in tumorigenesis is just starting to be elucidated.
Keywords: circRNA, noncoding RNA, esophageal squamous cell carcinoma, breast cancer, biomarker
This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.Download Article [PDF] View Full Text [HTML][Machine readable]