Integrated Analysis of Long Noncoding RNA and mRNA Expression Profile in Advanced Laryngeal Squamous Cell Carcinoma

被引:55
作者
Feng, Ling [1 ,2 ]
Wang, Ru [1 ,2 ]
Lian, Meng [1 ,2 ]
Ma, Hongzhi [1 ,2 ]
He, Ning [1 ,3 ]
Liu, Honggang [4 ]
Wang, Haizhou [1 ,2 ]
Fang, Jugao [1 ,2 ,4 ]
机构
[1] Capital Med Univ, Dept Otorhinolaryngol Head & Neck Surg, Beijing Tongren Hosp, Beijing, Peoples R China
[2] Minist Educ, Key Lab Otorhinolaryngol Head & Neck Surg, Beijing, Peoples R China
[3] Peoples Hosp Guangxi Zhuang Autonomous Reg, Dept Head & Neck Surg, Nanning, Guangxi, Peoples R China
[4] Beijing Key Lab Head & Neck Mol Diagnost Pathol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; GASTRIC-CANCER; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; PROTEIN EXPRESSION; METASTASIS; GENE; PROLIFERATION; PROMOTES; PATHWAY;
D O I
10.1371/journal.pone.0169232
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Long non-coding RNA (IncRNA) plays an important role in tumorigenesis. However, the expression pattern and function of IncRNAs in laryngeal squamous cell carcinoma (LSCC) are still unclear. To investigate the aberrantly expressed IncRNAs and mRNAs in advanced LSCC, we screened IncRNA and mRNA expression profiles in 9 pairs of primary Stage IVA LSCC tissues and adjacent non-neoplastic tissues by IncRNA and mRNA integrated micro-arrays. Gene Ontology and pathway analysis were performed to find out the significant function and pathway of the differentially expressed mRNAs, gene-gene functional interaction network and ceRNA network were constructed to select core mRNAs, and IncRNA-mRNA expression correlation network was built to identify the interactions between IncRNA and mRNA. qRT-PCR was performed to further validate the expressions of selected IncRNAs and mRNAs in advanced LSCC. We found 1459 differentially expressed IncRNAs and 2381 differentially expressed mRNAs, including 846 up-regulated IncRNAs and 613 down-regulated IncRNAs, 1542 up-regulated mRNAs and 839 down-regulated mRNAs. The mRNAs ITGB1, HIFI A, and DDIT4 were selected as core mRNAs, which are mainly involved in biological processes, such as matrix organization, cell cycle, adhesion, and metabolic pathway. LncRNA-mRNA expression correlation network showed LncRNA NR_027340, MIR31HG were positively correlated with ITGB1, HIF1A respectively. LncRNA SOX2-OT was negatively correlated with DDIT4. qRT-PCR further validated the expression of these IncRNAs and mRNAs. The work provides convincing evidence that the identified IncRNAs and mRNAs are potential biomarkers in advanced LSCC for further future studies.
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页数:17
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