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pmid:30714675

Long noncoding RNAs predict the survival of patients with colorectal cancer as revealed by constructing an endogenous RNA network using bioinformation analysis.

Hui Zhang · Zhuo Wang · Jianzhong Wu · Rong Ma · Jifeng Feng

Cancer medicine · 2019 doi:10.1002/cam4.1813

Paper

complete

Experiment

complete

Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:30714675
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2026-11-01T15:40:41Z
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2026-11-01T22:43:46Z
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paper object · 10 fields
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title
Long noncoding RNAs predict the survival of patients with colorectal cancer as revealed by constructing an endogenous RNA network using bioinformation analysis.
doi
10.1002/cam4.1813
pmid
30714675
authors array · 5 items
[0]
Hui Zhang
[1]
Zhuo Wang
[2]
Jianzhong Wu
[3]
Rong Ma
[4]
Jifeng Feng
journal
Cancer medicine
year
2019
abstract
Long noncoding RNAs (lncRNAs) are aberrantly expressed in various cancers types and can function as competing endogenous RNAs (ceRNAs), which promote and maintain tumor initiation and progression. In this study, we explored the functional roles and regulatory mechanisms of lncRNAs as ceRNAs in colorectal cancer and their clinical potential as biomarkers. The RNA sequencing profiles of patients with colorectal cancer were downloaded from TCGA database, and 62 lncRNAs, 30miRNAs, and 59 mRNAs were identified to comprise the ceRNA network (fold change > 2, P < 0.01). Functional enrichment analysis suggested that the target genes of the ceRNA network may be involved in the pathways related to cancer, including the signaling pathway that regulates the pluripotency of stem cells, wnt signaling pathway, hippo signaling pathway, basal cell carcinoma, and colorectal cancer. Univariate and multivariate Cox's proportional hazard regression model revealed that five (H19, MIR31HG, HOTAIR, WT1-AS, and LINC00488) out of 62 lncRNAs were closely related to the overall survival (OS) (P < 0.05). Furthermore, the five-lncRNA model could be an independent prognostic model in colorectal cancer. We computed for the risk function and constructed a risk score based on the five lncRNAs. Results showed that patients with high-risk scores have poor survival rates. Additionally, combing the risk score and other clinicopathological features, we can better predict the patient's survival probabilities. Furthermore, we validate our model in the GSE38832 dataset. Collectively, our study has provided a deeper understanding of the lncRNA-related ceRNA regulatory mechanism in CRC and identified five-lncRNA model, which could be considered as candidate prognostic biomarkers and therapeutic targets.
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The RNA‐Seq data and clinical information of CRC patients were completely downloaded from The Cancer Genome Atlas (TCGA) database (https://cancergenome.nih.gov/).
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The RNA‐Seq data and clinical information of CRC patients were completely downloaded from The Cancer Genome Atlas (TCGA) database (https://cancergenome.nih.gov/).
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NFAT transcriptional activity is associated with metastatic capacity in colon cancer
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Building a predictive model for prognosis and survival
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Combining risk score with clinical significance prognostic prediction for CRC
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The correlations between the five‐lncRNA model and clinical features
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Combining risk score with clinical significance prognostic prediction for CRC
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The correlations between the five‐lncRNA model and clinical features
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The DERNA (DElncRNAs, DEmRNAs, and DEmiRNAs) data between tumor and normal samples were analyzed using “edgeR” package in R.
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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fdr_bh
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capability object · 4 fields
tier
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capability:computational_analysis
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data object · 6 fields
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The RNA‐Seq data and clinical information of CRC patients were completely downloaded from The Cancer Genome Atlas (TCGA) database (https://cancergenome.nih.gov/).
basis
The paper names GSE38832 in Gene Expression Omnibus (GEO) Datasets of NCBI and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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normalise_counts
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fdr_bh
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their clinical potential as biomarkers. The RNA sequencing profiles of patients with colorectal cancer
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Complete file
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In this study, we explored the functional roles and regulatory mechanisms of lncRNAs as ceRNAs in colorectal cancer and their clinical potential as biomarkers. The RNA sequencing profiles of patients with colorectal cancer were downloaded from TCGA database, and 62 lncRNAs, 30miRNAs, and 59 mRNAs were identified to comprise the ceRNA network (fold change > 2, P < 0.01). Functional enrichment analysis suggested that the target genes of the ceRNA network may be involved in the pathways related to cancer, including the signaling pathway that regulates the pluripotency of stem cells, wnt signaling pathway, hippo signaling pathway, basal cell carcinoma, and colorectal cancer. Univariate and multivariate Cox's proportional hazard regression model revealed that five (H19, MIR31HG, HOTAIR, WT1-AS, and LINC00488) out of 62 lncRNAs were closely related to the overall survival (OS) (P < 0.05). Furthermore, the five-lncRNA model could be an independent prognostic model in colorectal cancer. We computed for the risk function and constructed a risk score based on the five lncRNAs. Results showed that patients with high-risk scores have poor survival rates. Additionally, combing the risk score and other clinicopathological features, we can better predict the patient's survival probabilities. Furthermore, we validate our model in the GSE38832 dataset. 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