LncRNA C7orf13 facilitates cell proliferation and metastasis in nasopharyngeal carcinoma via targeting miR-449c/miR-28-5p-FMNL2 axis

被引:0
|
作者
Xie, Peng [1 ]
Zhang, Yujie [1 ]
Shang, Jin [2 ]
Yu, Hanxu [3 ]
Du, Mingyu [1 ]
Shu, Jian [4 ]
Wei, Qiang [1 ]
Zhu, Zeyu [5 ,6 ]
He, Xia [1 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Jiangsu Inst Canc Res, Jiangsu Canc Hosp, 42 Baiziting Rd, Nanjing, Jiangsu, Peoples R China
[2] Dept Stomatol, Yangzhou, Peoples R China
[3] Nanjing Med Univ, Lianshui Cty Peoples Hosp, Affiliated Kangda Coll, Dept Radiotherapy, Huaian, Peoples R China
[4] Dept Radiotherapy, Sihong, Peoples R China
[5] Huaian Hosp Huaian City, Dept Orthoped, 161 Huailou East Rd, Huaian, Jiangsu, Peoples R China
[6] Huaian Canc Hosp, 161 Huailou East Rd, Huaian, Jiangsu, Peoples R China
来源
PRECISION MEDICAL SCIENCES | 2024年 / 13卷 / 04期
关键词
C7orf13; FMNL2; miR-28-5p; miR-449c; nasopharyngeal carcinoma; NONCODING RNA; CANCER;
D O I
10.1002/prm2.12152
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study was to determine the involvement of long non-coding RNA C7orf13 in nasopharyngeal carcinoma (NPC) and its underlying mechanism. Real-time quantitative PCR results indicated that C7orf13 was overexpressed in NPC and associated with malignant features. C7orf13 knockdown significantly suppressed the proliferation, migration and invasion of NPC cells. Furthermore, we found that C7orf13 sequestered miR-449c and miR-28-5p in NPC cells by dual-luciferase reporter assays and RNA immunoprecipitation analysis. Sequent experiments showed that C7orf13 has a positive relationship with formin-like 2 (FMNL2) in NPC tissues. Moreover, C7orf13 knockdown weakened FMNL2-mediated cell invasion and migration. Finally, functional experiments revealed that the positive effect of C7orf13 on cell migration and invasion was mediated by the miR-449c/miR-28-5p-FMNL2 axis. Generally, our study identifies the biological role of long non-coding RNA C7orf13 in the malignant process of NPC, which may pave a new way for the diagnosis and treatment of NPC.
引用
收藏
页码:204 / 213
页数:10
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