Analysis of the Cancer Genome Atlas Data Reveals Novel Putative ncRNAs Targets in Hepatocellular Carcinoma

被引:18
作者
Falcon, Tiago [1 ]
Freitas, Martiela [1 ,2 ]
Mello, Ana Carolina [1 ,3 ]
Coutinho, Laura [1 ,3 ]
Alvares-da-Silva, Mario R. [4 ,5 ]
Matte, Ursula [1 ,2 ,6 ]
机构
[1] Hosp Clin Porto Alegre, Gene Therapy Ctr, Expt Res Ctr, BR-90035903 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Postgrad Program Genet & Mol Biol, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Grad Program Biotechnol Bioinformat, BR-91501970 Porto Alegre, RS, Brazil
[4] Hosp Clin Porto Alegre, Gastroenterol & Hepatol Div, Porto Alegre, RS, Brazil
[5] Univ Fed Rio Grande do Sul, Dept Internal Med, Grad Program Gastroenterol & Hepatol, Porto Alegre, RS, Brazil
[6] Univ Fed Rio Grande do Sul, Dept Genet, BR-91501970 Porto Alegre, RS, Brazil
关键词
INFLAMMASOME ACTIVATION; EXPRESSION PATTERNS; CELL-PROLIFERATION; PROSTATE-CANCER; AQUAPORIN; 9; MICRORNAS; RNA; INVASION; PYROPTOSIS; CYTOSCAPE;
D O I
10.1155/2018/2864120
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hepatocellular carcinoma (HCC) is the prevalent type of primary liver malignancy. Different noncoding RNAs (ncRNAs) that negatively regulate gene expression, such as the micro RNAs and the long ncRNAs (IncRNAs), have been associated with cell invasiveness and cell dissemination, tumor recurrence, and metastasis in HCC. To evaluate which regulatory ncRNAs might be good candidates to disrupt HCC proliferation pathways, we performed both unsupervised and supervised analyses of HCC expression data, comparing samples of solid tumor tissue (TP) and adjacent tissue (NT) of a set of patients, focusing on ncRNAs and searching for common mechanisms that may shed light in future therapeutic options. All analyses were performed using the R software. Differential expression (total RNA and miRNA) and enrichment analyses (Gene Ontology + Pathways) were performed using the package TCGABiolinks. As a result, we improved the set of lncRNAs that could be the target of future studies in HCC, highlighting the potential of FAM170B-AS1 and TTN-AS1.
引用
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页数:9
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