Hepatocellular carcinoma-related lncRNAs in different human races in the TCGA database: Screening and prediction of their functions
10.16571/j.cnki.1008-8199.2019.10.006
- VernacularTitle: TCGA数据库中不同种族肝细胞癌相关lncRNAs的筛选及功能预测
- Author:
Jia-kang MA
1
;
Kai-kai REN
1
;
Yu-meng LI
1
;
Nan LI
1
;
Ling ZHANG
;
Jian WANG
1
;
Jin-qi SUN
2
;
Bo ZHOU
3
;
Jun MA
3
Author Information
1. Department of Oncology, 2
2. Institute of Digestive Diseases, Zhengzhou University, Zhengzhou 450014, Henan,China
3. Hepatobiliary Pancreatic Surgery, Henan Cancer Hospital, Zhengzhou 450008,Henan,China
- Publication Type:Journal Article
- Keywords:
hepatocellular carcinoma;
long non-coding RNAs (lncRNAs);
TCGA;
ceRNA;
overall survival;
race
- From:
Journal of Medical Postgraduates
2019;32(10):1037-1042
- CountryChina
- Language:Chinese
-
Abstract:
Objective Differentially-expressed lncRNAs in hepatocellular carcinoma (HCC) among different races remain unclarified at present time. This study aimed to analyze the shared and specific differential expression profiles of lncRNAs in HCC patients of the yellow, white and black races in the TCGA database and predict their functions and regulatory mechanisms. Methods We screened differentially expressed lncRNAs in the cancer and paracancer tissues of the HCC patients of the yellow, white and black races, compared differential expression profiles of lncRNAs and identified the common differentially expressed lncRNAs among the three races. We performed COX regression survival analysis on the differentially expressed lncRNAs, constructed a ceRNA network, and predicted the target genes and their regulatory mechanisms by GO and KEGG enrichment analyses and prediction of the transcription factors. Results Totally 49 HCC-related lncRNAs were found in all the three races, with 21.5% overlapped in the white and black races, 7.8% in the white and yellow and 5.8% in the black and Asians. GO enrichment analysis showed that the target genes of LINC01224 in the all three races were related to DNA replication and transposition, gene expression regulation, epigenetics, silencing of miRNAs, and gene silencing after RNA transcription, while KEGG analysis revealed a correlation of LINC01224 with the cell cycle and DNA replication. Target genes were not predicted in the 11 survival-related lncRNAs in the patients of the white race. Of the 6 survival-related lncRNAs in the yellow patients, the target gene of AC093609.1 was shown to be involved in the activity of the ionic channel, regulation of cardiomyopathy- and cardiomyocyte adrenalin-related signaling pathways, various metabolic functions, fat degradation, ABC protein transportation, and amino acid metabolism. Conclusion HCC-related expression profiles of lncRNAs have a great similarity between the white and black races, but a high differentiality between the yellow and the white or black. LINC01224 may be involved in the relation of tumor growth in all the three races, while AC093609.1 and AC126118.1 specific of the yellow race play an important role in tumor metabolism.
