Research Papers:
Identification of potential long non-coding RNA biomarkers associated with the progression of colon cancer
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Abstract
Jingwen Li1,*, Weinan Xue1,*, Junli Lv2,*, Peng Han1, Yanlong Liu1 and Binbin Cui1
1Department of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin 150081, China
2Department of Science, Harbin Medical University Cancer Hospital, Harbin 150081, China
*These authors contributed equally to this work
Correspondence to:
Binbin Cui, email: [email protected]
Yanlong Liu, email: [email protected]
Keywords: biomarkers, colon cancer, disease progression, long non-coding RNA
Received: March 29, 2017 Accepted: May 03, 2017 Published: May 17, 2017
ABSTRACT
Increasing evidence has suggested that dysregulated lncRNA expression played important roles in the development and progression of human cancers. Although prognostic roles of lncRNAs have been recognized for colon cancer (CC) patients, the search for novel lncRNA biomarkers potentially involved in CC progression is an urgent and still largely unmet medical need. In this study, we evaluated the lncRNA expression changes during the progression of CC by analyzing two cohorts of previously published expression profiles of CC patients and identified hundreds of differentially expressed lncRNAs. Then we identified eight lncRNAs that closely associated with the progression of CC patients from a large number of significantly altered lncRNAs using random forest supervised classification algorithm. Finally, an SVM-based lncRNA risk classifier was developed to discriminate high-risk CC patients from persons with early-stage and validated in both the training dataset and testing dataset by survival analysis and five-fold cross-validation strategy. Our pathway enrichment analysis based on protein-coding genes that are co-expressed with lncRNAs, suggested that variation in expression of eight lncRNAs biomarkers might affect critical pathways involved in CC progression. With further validation, these eight lncRNAs might have significant implications for the clinical management of CC patients with early stage and improve our understanding of cancer progression.
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