| Literature DB >> 27380926 |
Fan Yang1, Ye-Huan Liu1, Si-Yang Dong1, Zhi-Han Yao1, Lin Lv1, Rui-Min Ma1, Xuan-Xuan Dai1, Jiao Wang2, Xiao-Hua Zhang3, Ou-Chen Wang4.
Abstract
Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer with unfavorable outcome. It is urgent to explore novel biomarkers and potential therapeutic targets in this malignancy. Increasing knowledge of long noncoding RNAs (lncRNAs) significantly deepens our understanding of cancer biology. Here, we sequenced eight paired TNBC tumor tissues and non-cancerous tissues, and validated significantly differentially expressed lncRNAs. Gene ontology (GO) and pathway analysis were used to investigate the function of differentially expressed mRNAs. Further, potential core lncRNAs in TNBC were identified by co-expression networks. Kaplan-Meier analysis also indicated that breast cancer patients with lower expression level of rhabdomyosarcoma 2 associated transcript (RMST), one of the potential core lncRNAs, had worse overall survival. To the best of our knowledge, it was the first report that RMST was involved in breast cancer. Our research provided a rich resource to the research community for further investigating lncRNAs functions and identifying lncRNAs with diagnostic and therapeutic potentials in TNBC.Entities:
Keywords: Expression profile; Long non-coding RNA; RMST; Triple-negative breast cancer
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Year: 2016 PMID: 27380926 DOI: 10.1016/j.gene.2016.07.002
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688