Abstract

BackgroundRadioresistance is one of the main obstacle limiting the therapeutic efficacy and prognosis of patients, the molecular mechanisms of radioresistance is still unclear. The purpose of this study was to identify the key genes and miRNAs and to explore their potential molecular mechanisms in radioresistant nasopharyngeal carcinoma.MethodsIn this study, we analysis the differentially expressed genes and microRNA based on the database of GSE48501 and GSE48502, and then employed bioinformatics to analyze the pathways and GO terms in which DEGs and DEMS target genes are involved. Moreover, Construction of protein-protein interaction network and identification of hub genes. Finally, analyzed the biological networks for validated target gene of hub miRNAs.ResultsA total of 373 differentially expressed genes (DEGs) and 14 differentially expressed microRNAs (DEMs) were screened out. The up-regulated gene JUN was overlap both in DEGs and publicly available studies, which was potentially targeted by three miRNAs, including hsa-miR-203, hsa-miR-24 and hsa-miR-31. Moreover, Pathway analysis showed that both up-regulated gene and DEMs target genes were enriched in TGF-beta signaling pathway, Hepatitis B, Pathways in cancer and p53 signaling pathway. Finally, we further constructed protein-protein interaction network (PPI) of DEGs and analyzed the biological networks for above mentioned common miRNAs, the result indicated that JUN was a core hub gene in PPI network, hsa-miR-24 and its target gene were significantly enriched in P53 signaling pathway.ConclusionsThese results might provide new clues to improve the radiosensitivity of Nasopharyngeal Carcinoma.

Highlights

  • Radioresistance is one of the main obstacle limiting the therapeutic efficacy and prognosis of patients, the molecular mechanisms of radioresistance is still unclear

  • These results might provide new clues to improve the radiosensitivity of Nasopharyngeal Carcinoma

  • differentially expressed genes (DEGs) and differentially expressed microRNAs (DEMs) in radioresistant nasopharyngeal carcinoma (NPC) cells compared with radioresistant NPC cells GEO2R analyzed result shown that a total of 373 DEGs were identified in radioresistant NPC cells, including 291 mRNAs were up-regulated and 82 mRNAs were down-regulated (Table 1)

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Summary

Introduction

Radioresistance is one of the main obstacle limiting the therapeutic efficacy and prognosis of patients, the molecular mechanisms of radioresistance is still unclear. The purpose of this study was to identify the key genes and miRNAs and to explore their potential molecular mechanisms in radioresistant nasopharyngeal carcinoma. Identifying potential biomarkers and studying the molecular mechanisms associated with radioresistant nasopharyngeal carcinoma has become a hot topic both in basic and clinical research. We analysis the differentially expressed genes and microRNA between radioresistant NPC CNE2-R cells and radiosensitive CNE2 cells based on the database of GSE48501 and GSE48502, and employed bioinformatics to analyze the pathways and GO terms in which DEGs and DEMS target genes are involved. Analyzed the biological networks for validated target gene of hub miRNAs. Our data may provide an important contribution to identified biological markers and clarify the mechanisms of NPC radioresistance

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