Investigating the Long Non-Coding RNA Expression Profiles in the development of esophageal cancer: Insights from genomic Analysis

سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 81

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شناسه ملی سند علمی:

JR_JHGG-6-2_001

تاریخ نمایه سازی: 1 شهریور 1403

چکیده مقاله:

Background: Esophageal carcinoma (ESCA) is one of the most common types of cancer. ESCA accounted for the sixth leading cause of cancer-related deaths globally. Most patients are diagnosed at late stages of ESCA, with distance metastasis or chemoresistance, which leads to a poor prognosis. Previous studies demonstrated lncRNA presentation and roles in ESCA cells and patients' tissue. It has been proposed that lncRNAs can be considered a new prognostic and diagnostic biomarker in ESCA. In this study, we comprehensively explored the interaction of lncRNAs with miRNAs and mRNAs of the TCGA database and proposed a novel promising biomarker with good diagnostic and prognostic values. Methods: The public data of RNA-seq, miR-seq, and related clinical data were downloaded from the TCGA database. Differential expression analysis was conducted by “limma” in R. GO, and KEGG signaling pathways were used for enrichments. STRING database was used for PPI analysis. CE-network was constructed by the STAR database in R. Kaplan-Meier survival analysis (log-rank test), and ROC curve analysis was used to indicate the diagnostic and prognostic values of the biomarkers. Results: Differentially expressed data illustrated that ۴۵.۸% of the total mRNAs in the data related to ESCA patients showed increased expression and ۵۴.۲% decreased expression. The GO and KEGG pathway analysis showed that the differentially expressed mRNAs were enriched in critical biological processes. Important protein-protein interaction hubs were identified. The ceRNA network data demonstrated critical lncRNAs essential in ESCA development, including TMEM۱۶B-AS۱, AC۰۹۳۰۱۰.۳, SNHG۳, and PVT۱. The data revealed that the lncRNA WDFY۳-AS۲, AC۱۰۸۴۴۹.۲, DLEU۲, AC۰۰۷۱۲۸.۱, and AP۰۰۳۳۵۶.۱ are potential diagnostic and prognostic biomarkers in ESCA patients. Conclusion: Altogether, this study demonstrates lncRNA, miRNA, and mRNA interaction and mentions regulatory networks which can be considered as a therapeutic option in ESCA. In addition, we proposed potential diagnostic and prognostic biomarkers for ESCA patients.

نویسندگان

Mehran Gholamin

Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mojtaba Jafarinia

Department of Biology, Marvdasht Branch, Islamic Azad University, Marvdasht, Iran.

Mohammad Kargar

Department of Microbiology, Jahrom Branch, Islamic Azad University, Jahrom, Iran

Samaneh Talebi

Department of Genetics, Marvdasht Branch, Islamic Azad University, Marvdasht, Iran;

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