Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma

The clinical significance and potential targets of miR-150-5p have not been elucidated in nasopharyngeal carcinoma (NPC). The pooled analysis based on 539 NPC samples and 75 non-NPC nasopharyngeal samples demonstrated that the expression of miR-150-5p was down-regulated in NPC, with the area under t...

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Main Authors: Jia-Ying Wen, Gang Chen, Jian-Di Li, Jia-Yuan Luo, Juan He, Ren-Sheng Wang, Li-Ting Qin
Format: Article
Language:English
Published: Hindawi - Cambridge University Press 2022-01-01
Series:Genetics Research
Online Access:http://dx.doi.org/10.1155/2022/2485055
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author Jia-Ying Wen
Gang Chen
Jian-Di Li
Jia-Yuan Luo
Juan He
Ren-Sheng Wang
Li-Ting Qin
author_facet Jia-Ying Wen
Gang Chen
Jian-Di Li
Jia-Yuan Luo
Juan He
Ren-Sheng Wang
Li-Ting Qin
author_sort Jia-Ying Wen
collection DOAJ
description The clinical significance and potential targets of miR-150-5p have not been elucidated in nasopharyngeal carcinoma (NPC). The pooled analysis based on 539 NPC samples and 75 non-NPC nasopharyngeal samples demonstrated that the expression of miR-150-5p was down-regulated in NPC, with the area under the curve being 0.89 and the standardized mean difference being −0.66. Subsequently, we further screened the differentially expressed genes (DEGs) of 14 datasets, including 312 NPC samples and 70 non-NPC nasopharyngeal samples. After the DEGs were narrowed down with the predicted targets from the miRWalk database, 1316 prospective target genes of miR-150-5p were identified. The enrichment analysis suggested that “pathways in cancer” was the most significant pathway. Finally, six hub genes of “pathways in cancer”, including EGFR, TP53, HRAS, CCND1, CDH1, and FGF2, were screened out through the STRING database. In conclusion, the down-regulation of miR-150-5p modulates the tumorigenesis and progression of NPC.
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spelling doaj.art-6a878c6aedb94e61bec510ea5b125d632022-12-22T04:30:45ZengHindawi - Cambridge University PressGenetics Research1469-50732022-01-01202210.1155/2022/2485055Downregulated miR-150-5p in the Tissue of Nasopharyngeal CarcinomaJia-Ying Wen0Gang Chen1Jian-Di Li2Jia-Yuan Luo3Juan He4Ren-Sheng Wang5Li-Ting Qin6Department of RadiotherapyDepartment of PathologyDepartment of PathologyDepartment of PathologyDepartment of PathologyDepartment of RadiotherapyDepartment of PathologyThe clinical significance and potential targets of miR-150-5p have not been elucidated in nasopharyngeal carcinoma (NPC). The pooled analysis based on 539 NPC samples and 75 non-NPC nasopharyngeal samples demonstrated that the expression of miR-150-5p was down-regulated in NPC, with the area under the curve being 0.89 and the standardized mean difference being −0.66. Subsequently, we further screened the differentially expressed genes (DEGs) of 14 datasets, including 312 NPC samples and 70 non-NPC nasopharyngeal samples. After the DEGs were narrowed down with the predicted targets from the miRWalk database, 1316 prospective target genes of miR-150-5p were identified. The enrichment analysis suggested that “pathways in cancer” was the most significant pathway. Finally, six hub genes of “pathways in cancer”, including EGFR, TP53, HRAS, CCND1, CDH1, and FGF2, were screened out through the STRING database. In conclusion, the down-regulation of miR-150-5p modulates the tumorigenesis and progression of NPC.http://dx.doi.org/10.1155/2022/2485055
spellingShingle Jia-Ying Wen
Gang Chen
Jian-Di Li
Jia-Yuan Luo
Juan He
Ren-Sheng Wang
Li-Ting Qin
Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
Genetics Research
title Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
title_full Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
title_fullStr Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
title_full_unstemmed Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
title_short Downregulated miR-150-5p in the Tissue of Nasopharyngeal Carcinoma
title_sort downregulated mir 150 5p in the tissue of nasopharyngeal carcinoma
url http://dx.doi.org/10.1155/2022/2485055
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