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

被引:3
|
作者
Wen, Jia-Ying [1 ]
Chen, Gang [2 ]
Li, Jian-Di [2 ]
Luo, Jia-Yuan [2 ]
He, Juan [2 ]
Wang, Ren-Sheng [1 ]
Qin, Li-Ting [2 ]
机构
[1] Guangxi Med Univ, Dept Radiotherapy, Affiliated Hosp 1, 6 Shuangyong Rd, Nanning 530021, Guangxi Zhuang, Peoples R China
[2] Guangxi Med Univ, Dept Pathol, Affiliated Hosp 1, 6 Shuangyong Rd, Nanning 530021, Guangxi Zhuang, Peoples R China
关键词
CELL-PROLIFERATION; TREATMENT OUTCOMES; CCND1; EXPRESSION; CANCER; METASTASIS; RECEPTOR; PROMOTES;
D O I
10.1155/2022/2485055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页数:13
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