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Bioinformatic Analysis Identified Potentially Prognostic Long Noncoding RNAs and MicroRNAs for Gastric Cancer
Jiao Guo1, Yongda Liu1, Ping Zhao1
1Department of Anesthesiology, Shengjing Hospital of China Medical University, No. 36, Sanhao Street, Heping District, Shenyang, 110004 Liaoning Province, China.
Biomed Research International
|December 20, 2021
Summary
This study identifies five long noncoding RNAs (lncRNAs) and two microRNAs (miRNAs) as independent prognostic indicators for gastric cancer (GC). These biomarkers, along with clinical factors, offer potential for improved GC diagnosis and therapy.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Gastric cancer (GC) is a leading global malignancy.
- Identifying novel diagnostic and therapeutic targets is crucial for improving patient outcomes.
Purpose of the Study:
- To identify potential diagnostic and therapeutic long noncoding RNAs (lncRNAs) and microRNAs (miRNAs) for gastric cancer (GC).
- To investigate the prognostic value of differentially expressed lncRNAs (DElncRNAs) and miRNAs (DEmiRNAs) in GC.
Main Methods:
- Utilized The Cancer Genome Atlas (TCGA) database for GC data (187 tumor tissues, 32 non-tumor tissues).
- Employed RStudio/Bioconductor for univariate analysis, LASSO Cox, and multivariate Cox regression.
- Performed Kaplan-Meier survival analysis and pathway enrichment analysis.
Main Results:
- Identified five lncRNAs (AC007785.3, AC079385.3, LINC00392, LINC01729, U95743.1) and two miRNAs (hsa-miR-3174, hsa-miR-605) as independent prognostic indicators for GC.
- AC007785.3, AC079385.3, LINC01729, miR-3174, and miR-605 significantly correlated with overall survival (OS).
- Target genes clustered in MAPK and cGMP-PKG signaling pathways; AC007785.3 associated with metastasis, miR-3174 with primary tumor status.
Conclusions:
- Five lncRNAs and two miRNAs were identified as independent prognostic markers for GC.
- These identified molecules, alongside clinical factors, are related to GC pathogenesis and prognosis.
- The findings provide potential entry points for developing novel prognostic markers for GC.
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