Cargando…

Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network

BACKGROUND: Long noncoding RNAs (lncRNAs) can play vital roles in tumor initiation, progression, invasion, and metastasis. However, the functional role of the lncRNA-based competing endogenous RNA (ceRNA) networks in gastric cancer (GC) is still unclear. We aimed to identify novel lncRNAs and their...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Min, Li, Jing, Huang, Zhengkai, Li, Yuejun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798172/
https://www.ncbi.nlm.nih.gov/pubmed/35117756
http://dx.doi.org/10.21037/tcr-19-2977
_version_ 1784641736369242112
author Liu, Min
Li, Jing
Huang, Zhengkai
Li, Yuejun
author_facet Liu, Min
Li, Jing
Huang, Zhengkai
Li, Yuejun
author_sort Liu, Min
collection PubMed
description BACKGROUND: Long noncoding RNAs (lncRNAs) can play vital roles in tumor initiation, progression, invasion, and metastasis. However, the functional role of the lncRNA-based competing endogenous RNA (ceRNA) networks in gastric cancer (GC) is still unclear. We aimed to identify novel lncRNAs and their association with GC prognosis. METHODS: The lncRNA, miRNA, and mRNA expression profiles of GC patients data were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed genes (DEGs) were identified using the edge-R package. Then, the relationship among lncRNAs-miRNAs-mRNAs was integrated into a constructed ceRNA network with Cytoscape software. Using Cox regression analysis, a risk score system based on DEGs associated with patient prognosis in GC was established. Finally, a nomogram was founded to predict the prognosis of GC patients. RESULTS: A total of 971 differentially expressed lncRNAs (DElncRNAs), 144 differentially expressed miRNAs (DEmiRNAs) and 2,789 differentially expressed mRNAs (DEmRNAs) were identified and found to be associated with GC risk. Using the bioinformatics method, a ceRNA network involving 62 DElncRNAs, 21 DEmiRNAs and 59 DEmRNAs was constructed. Based on the results of the Cox regression analysis, a risk-scoring system involving 3 lncRNAs (i.e., ADAMTS9-AS1, C15orf54, and AL391152.1) was set up for the survival analysis of GC patients. The area under the receiver operating characteristic (ROC) curve for the risk-scoring system was 0.674, with a C-index of 0.64 [95% confidence interval (CI): 0.59–0.69, P=2.806485e−08]. Univariate and multivariate Cox regression analyses demonstrated that the risk-scoring system was an independent prognostic factor for GC. The risk-scoring system is positively associated with advanced tumor grade. The expression of these 3 lncRNAs were validated in GEPIA database. A nomogram based on these 3 lncRNAs was created to predict the prognosis of GC patients. CONCLUSIONS: Our study established a novel lncRNA-expression-based ceRNA network and an ADAMTS9-AS1-C15orf54-AL391152.1-based risk-scoring system, which can be used to predict the prognosis of GC patients.
format Online
Article
Text
id pubmed-8798172
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-87981722022-02-02 Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network Liu, Min Li, Jing Huang, Zhengkai Li, Yuejun Transl Cancer Res Original Article BACKGROUND: Long noncoding RNAs (lncRNAs) can play vital roles in tumor initiation, progression, invasion, and metastasis. However, the functional role of the lncRNA-based competing endogenous RNA (ceRNA) networks in gastric cancer (GC) is still unclear. We aimed to identify novel lncRNAs and their association with GC prognosis. METHODS: The lncRNA, miRNA, and mRNA expression profiles of GC patients data were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed genes (DEGs) were identified using the edge-R package. Then, the relationship among lncRNAs-miRNAs-mRNAs was integrated into a constructed ceRNA network with Cytoscape software. Using Cox regression analysis, a risk score system based on DEGs associated with patient prognosis in GC was established. Finally, a nomogram was founded to predict the prognosis of GC patients. RESULTS: A total of 971 differentially expressed lncRNAs (DElncRNAs), 144 differentially expressed miRNAs (DEmiRNAs) and 2,789 differentially expressed mRNAs (DEmRNAs) were identified and found to be associated with GC risk. Using the bioinformatics method, a ceRNA network involving 62 DElncRNAs, 21 DEmiRNAs and 59 DEmRNAs was constructed. Based on the results of the Cox regression analysis, a risk-scoring system involving 3 lncRNAs (i.e., ADAMTS9-AS1, C15orf54, and AL391152.1) was set up for the survival analysis of GC patients. The area under the receiver operating characteristic (ROC) curve for the risk-scoring system was 0.674, with a C-index of 0.64 [95% confidence interval (CI): 0.59–0.69, P=2.806485e−08]. Univariate and multivariate Cox regression analyses demonstrated that the risk-scoring system was an independent prognostic factor for GC. The risk-scoring system is positively associated with advanced tumor grade. The expression of these 3 lncRNAs were validated in GEPIA database. A nomogram based on these 3 lncRNAs was created to predict the prognosis of GC patients. CONCLUSIONS: Our study established a novel lncRNA-expression-based ceRNA network and an ADAMTS9-AS1-C15orf54-AL391152.1-based risk-scoring system, which can be used to predict the prognosis of GC patients. AME Publishing Company 2020-06 /pmc/articles/PMC8798172/ /pubmed/35117756 http://dx.doi.org/10.21037/tcr-19-2977 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Liu, Min
Li, Jing
Huang, Zhengkai
Li, Yuejun
Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title_full Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title_fullStr Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title_full_unstemmed Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title_short Gastric cancer risk-scoring system based on analysis of a competing endogenous RNA network
title_sort gastric cancer risk-scoring system based on analysis of a competing endogenous rna network
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798172/
https://www.ncbi.nlm.nih.gov/pubmed/35117756
http://dx.doi.org/10.21037/tcr-19-2977
work_keys_str_mv AT liumin gastriccancerriskscoringsystembasedonanalysisofacompetingendogenousrnanetwork
AT lijing gastriccancerriskscoringsystembasedonanalysisofacompetingendogenousrnanetwork
AT huangzhengkai gastriccancerriskscoringsystembasedonanalysisofacompetingendogenousrnanetwork
AT liyuejun gastriccancerriskscoringsystembasedonanalysisofacompetingendogenousrnanetwork