SP1-induced AFAP1-AS1 contributes to proliferation and invasion by regulating miR-497-5p/CELF1 pathway in nasopharyngeal carcinoma

被引:9
作者
Jin, Hui [1 ]
Liang, Gengtian [1 ]
Yang, Liping [1 ]
Liu, Li [1 ]
Wang, Binru [1 ]
Yan, Fengqin [2 ,3 ]
机构
[1] Wuhan Third Hosp, Dept Otolaryngol, Wuhan 430000, Hubei, Peoples R China
[2] Univ Chinese Acad Sci, Dept Head & Neck Radiat Therapy, Zhejiang Canc Hosp, Canc Hosp, 1 Banshan Rd, Hangzhou 310021, Zhejiang, Peoples R China
[3] Chinese Acad Sci, Inst Canc & Basic Med IBMC, Hangzhou 310021, Zhejiang, Peoples R China
关键词
Nasopharyngeal carcinoma; AFAP1-AS1; SP1; miR-497-5p; LONG NONCODING RNAS; CELL-PROLIFERATION; TUMOR-GROWTH; METASTASIS; CANCER; PROGRESSION; EXPRESSION;
D O I
10.1007/s13577-020-00475-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nasopharyngeal carcinoma is a type of otolaryngological malignancy with high incidence. Long non-coding RNAs (lncRNAs) are closely related to nasopharyngeal carcinoma. LncRNA AFAP1-AS1 (AFAP1-AS1) has been found to play important roles in nasopharyngeal carcinoma progression and poor prognosis. However, the mechanism underlying AFAP1-AS1 in regulating nasopharyngeal carcinoma is still unclear. In current study, AFAP1-AS1 was found to be up-regulated in nasopharyngeal carcinoma tissues and cells. AFAP1-AS1 overexpression and knockdown were conducted in nasopharyngeal carcinoma cells. The results proved that AFAP1-AS1 promoted the survival and migration of nasopharyngeal carcinoma cells. Additionally, specificity protein 1 (SP1) was enhanced in nasopharyngeal carcinoma tissues and cells, and induced AFAP1-AS1 expression. The interaction between AFAP1-AS1 and miR-497-5p was confirmed. AFAP1-AS1 was demonstrated to regulate CELF1, a target gene of miR-497-5p. Further functional analysis revealed that AFAP1-AS1 knockdown attenuated SP1-induced nasopharyngeal carcinoma progression. These results indicate that SP1-induced AFAP1-AS1 facilitates nasopharyngeal carcinoma progression by regulating miR-497-5p/CELF1 pathway, which provides a new target for nasopharyngeal carcinoma treatment.
引用
收藏
页码:491 / 501
页数:11
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