LINC00665 promotes Ovarian Cancer progression through regulating the miRNA-34a-5p/E2F3 axis

被引:16
|
作者
Xu, Dan [1 ,3 ]
Song, Qingxia [1 ]
Liu, Ying [1 ]
Chen, Wansu [1 ]
Lu, Lijuan [1 ]
Xu, Min [1 ]
Fang, Xiaohui [4 ]
Zhao, Wenjie [1 ]
Zhou, Huifang [2 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Dept Gynaecol, Suzhou TCM Hosp, Suzhou 215009, Peoples R China
[2] Nanjing Univ Chinese Med, Dept Gynaecol, Affiliated Hosp, Nanjing 210029, Peoples R China
[3] Nanjing Univ Chinese Med, Nanjing 210023, Peoples R China
[4] Nanjing Univ Chinese Med, Dept Clin Lab, Suzhou TCM Hosp, Suzhou 215009, Peoples R China
来源
JOURNAL OF CANCER | 2021年 / 12卷 / 06期
关键词
ovarian cancer; LINC00665; miRNA-34a-5p; E2F3;
D O I
10.7150/jca.51457
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To clarify the role of LINC00665 in ovarian cancer (OC) progression and the possible mechanism. Methods: LINC00665 levels in OC tissues and cell lines were detected by qRT-PCR. The correlation between LINC00665 and clinicopathologic characteristics of OC patients was assessed. Biological functions of OC cell phenotypes influenced by LINC00665 were examined by CCK-8, colony formation and Transwell assay. Dual-luciferase reporter assay and RIP assay were conducted to verify the interaction between LINC00665 and its downstream target. Results: LINC00665 was upregulated in OC and linked to poor prognosis. Knockdown of LINC00665 blocked malignant proliferative, migratory and invasive functions of OC cells. By competitively binding miRNA-34a-5p, LINC00665 abolished the inhibitory effect of miR-34a-3p on its downstream gene E2F3, thus promoting OC progression. Conclusion: LINC00665/miRNA-34a-5p/E2F3 axis is involved in OC progression, providing novel insights into the clinical treatment of OC.
引用
收藏
页码:1755 / 1763
页数:9
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