RNA sequencing and bioinformatics analysis of the long noncoding RNA-mRNA network in colorectal cancer

被引:19
作者
Zhang, Zheying [1 ]
Jia, Huijie [1 ]
Gu, Tengteng [1 ]
Hu, Qing [1 ]
Yu, Jian [2 ]
Zang, Dan [2 ]
Song, Na [3 ]
Wang, Haijun [1 ,2 ]
机构
[1] Xinxiang Med Univ, Sch Basic Med Sci, Dept Pathol, Jinsui Rd 601, Xinxiang 453003, Peoples R China
[2] Xinxiang Med Univ, Dept Pathol, Affiliated Hosp 1, Xinxiang, Peoples R China
[3] Xinxiang Med Univ, Sch Basic Med Sci, Dept Mol Biol & Biochem, Jinsui Rd 601, Xinxiang 453003, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; long noncoding RNA; long noncoding RNA-messenger RNA network; RNA sequencing; EXPRESSION ANALYSIS; METASTASIS; STRINGTIE; GROWTH; GENE;
D O I
10.1002/jcb.27319
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Long noncoding RNA (lncRNA) plays an important regulatory role in tumorigenesis. This study aims to analyze the lncRNA-messenger RNA (mRNA) expression network and potential roles in colorectal cancer (CRC). The LncRNA expression profile was analyzed in CRC tissue by RNA sequencing and the functions of differentially expressed genes were analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). The lncRNA-mRNA network was predicted with bioinformatics. From the result, we identified 485 differential expression lncRNAs and 2383 mRNAs in CRC, GO, and KEGG analyses showed that the changes in lncRNAs were mainly associated with metabolism and transcription regulation that were different from mRNA function. Additionally, based on the predicted coexpression network, we identified that NONHSAT074176.2, downregulated in CRC tissue and cell lines, was a hub lncRNA in the development of CRC. Our results describe the lncRNA-mRNA network in detail and indicate that lncRNA NONHSAT074176.2 may be useful as a candidate diagnostic biomarker and may be a promising therapeutic target for CRC.
引用
收藏
页码:9957 / 9966
页数:10
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