作者: Ming Wan , Fu-Min Zhang , Zheng-Long Li , Peng-Cheng Kang , Ping-Ming Jiang
DOI: 10.3892/OR.2016.4934
关键词:
摘要: Abstract Competing endogenous RNAs (ceRNAs) represent a novel layer regulations of long non-coding (lncRNAs) and genes that play important roles in cancer pathogenesis by binding microRNAs (miRNAs). However, the competition mechanism ceRNAs cholangiocarcinoma (CHOL) is not fully understood. In this study, we constructed dysregulated ceRNA competitive network (CCEN) to globally characterize competing difference between CHOL normal tissues. Then, integrated affinity propagation Kaplan‑Meier (K-M) methods identify functional clusters associated with survival. A total 7 key were identified. Further annotation analyses found Cluster23 Cluster32 involved cell based functions, loss relations may contribute CHOL, disturbing biological processes, such as 'Pathway cancer', MAPK Neurotrophin signaling pathway. This study provides further insights into understanding CHOL.