"Integrative Analysis Reveals Clinical Phenotypes and Oncogenic Potenti" by Ze-Lin Wang, Bin Li et al.
 

Keywords

lncRNA, expression profile, prognostification, somatic copy number alteration

Abstract

Long non-coding RNAs (lncRNAs) have been shown to contribute to tumorigenesis. However, surprisingly little is known about the comprehensive clinical and genomic characterization of lncRNAs across human cancer. In this study, we conducted comprehensive analyses for the expression profile, clinical outcomes, somatic copy number alterations (SCNAs) profile of lncRNAs in ~7000 clinical samples from 15 different cancer types. We identified significantly differentially expressed lncRNAs between tumor and normal tissues from each cancer. Notably, we characterized 47 lncRNAs which were extensively dysregulated in at least 10 cancer types, suggesting a conserved function in cancer development. We also analyzed the associations between lncRNA expressions and patient survival, and identified sets of lncRNAs that possessed significant prognostic values in specific cancer types. Our combined analysis of SCNA data and expression data uncovered 116 dysregulated lncRNAs are strikingly genomic altered across 15 cancer types, indicating their oncogenic potentials. Our study may lay the groundwork for future functional studies of lncRNAs and help facilitate the discovery of novel clinical biomarkers.

Original Publication Citation

Wang ZL, Li B, Piccolo SR, Zhang XQ, Li JH, Zhou H, Yang JH, Qu LH. Integrative analysis reveals clinical phenotypes and oncogenic potentials of long non-coding RNAs across 15 cancer types Oncotarget, 2016 Jun 7;7(23):35044-55. doi:10.18632/oncotarget.9037.

Document Type

Peer-Reviewed Article

Publication Date

2016-04-27

Publisher

Impact Journals

Language

English

College

Life Sciences

Department

Biology

University Standing at Time of Publication

Associate Professor

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