Research Papers:
Transcriptional profiling analysis and functional prediction of long noncoding RNAs in cancer
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Abstract
Jiao Yuan1,2,3,*, Haiyan Yue1,2,3,*, Meiying Zhang4, Jianjun Luo1,2, Lihui Liu1,2,3, Wei Wu1,2,3, Tengfei Xiao1,2, Xiaowei Chen1,2, Xiaomin Chen1,2, Dongdong Zhang1,2, Rui Xing5, Xin Tong6, Nan Wu5, Jian Zhao6,7, Youyong Lu5, Mingzhou Guo4, Runsheng Chen1,2
1Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China
2Beijing Key Laboratory of Noncoding RNA, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China
3University of Chinese Academy of Sciences, Beijing 100049, China
4Department of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing 100853, China
5Laboratory of Molecular Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China
6PLA General Hospital Cancer Center Key Laboratory, Medical School of Chinese PLA, Beijing 100853, China
7International Joint Cancer Institute, the Second Military Medical University, Shanghai 200433, China
*These authors have contributed equally to this work
Correspondence to:
Runsheng Chen, e-mail: [email protected]
Mingzhou Guo, e-mail: [email protected]
Youyong Lu, e-mail: [email protected]
Jian Zhao, e-mail: [email protected]
Keywords: IncRNA, expression, biomarker, gastric cancer, colon cancer
Received: August 10, 2015 Accepted: January 01, 2016 Published: January 23, 2016
ABSTRACT
Long noncoding RNAs (lncRNAs), which are noncoding RNAs (ncRNAs) with length more than 200 nucleotides (nt), have been demonstrated to be involved in various types of cancer. Consequently, it has been frequently discussed that lncRNAs with aberrant expression in cancer serve as potential diagnostic biomarkers and therapeutic targets. However, one major challenge of developing cancer biomarkers is tumor heterogeneity which means that tumor cells show different cellular morphology, metastatic potential as well as gene expression. In this study, a custom designed microarray platform covering both mRNAs and lncRNAs was applied to tumor tissues of gastric, colon, liver and lung. 316 and 157 differentially expressed (DE-) protein coding genes and lncRNAs common to these four types of cancer were identified respectively. Besides, the functional roles of common DE-lncRNAs were inferred based on their expression and genomic position correlation with mRNAs. Moreover, mRNAs and lncRNAs with tissue specificity were also identified, suggesting their particular roles with regard to specific biogenesis and functions of different organs. Based on the large-scale survey of mRNAs and lncRNAs in four types of cancer, this study may offer new biomarkers common or specific for various types of cancer.
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