RETRACTED: Testis developmental related gene 1 promotes non-small-cell lung cancer through the microRNA-214-5p/Kruppel-like factor 5 axis (Retracted Article)

被引:7
|
作者
Lu, Xudong [1 ,2 ]
Zhao, Nian [2 ]
Duan, Guangjun [2 ]
Deng, Zhiyong [3 ]
Lu, Yimin [1 ,2 ]
机构
[1] Soochow Univ, Suzhou, Jiangsu, Peoples R China
[2] Jiangsu Univ, Dept Pulm & Crit Care Med, Affiliated Kunshan Hosp, Kunshan, Jiangsu, Peoples R China
[3] Jiangsu Univ, Dept Sci & Technol, Affiliated Kunshan Hosp, Kunshan, Jiangsu, Peoples R China
关键词
TDRG1; miR-214-5p; KLF5; NSCLC; PROGRESSION;
D O I
10.1080/21655979.2021.2012406
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Non-small-cell lung cancer (NSCLC) is a frequent malignancy and has a high global incidence. Long noncoding RNAs (lncRNAs) are implicated in carcinogenesis and tumor progression. LncRNA testis developmental related gene 1 (TDRG1) plays a pivotal role in many cancers. This study researched the biological regulatory mechanisms of TDRG1 in NSCLC. Gene expression was assessed by reverse transcriptase quantitative polymerase chain reaction (RT-qPCR). Changes in the NSCLC cell phenotypes were examined using 5-ethynyl-2'-deoxyuridine (EdU), cell counting kit-8 (CCK-8), wound healing, flow cytometry, and Transwell assays. The binding capacity between TDRG1, microRNA-214-5p (miR-214-5p), and Kruppel-like factor 5 (KLF5) was tested using luciferase reporter and RNA immunoprecipitation (RIP) assays. In this study, we found that TDRG1 was upregulated in NSCLC samples. Functionally, TDRG1 depletion inhibited NSCLC cell growth, migration, and invasion and accelerated apoptosis. In addition, TDRG1 interacted with miR-2145p, and miR-214-5p directly targeted KLF5. The suppressive effect of TDRG1 knockdown on NSCLC cellular processes was abolished by KLF5 overexpression. Overall, TDRG1 exerts carcinogenic effects in NSCLC by regulating the miR-214-5p/KLF5 axis. [GRAPHICS]
引用
收藏
页码:603 / 616
页数:14
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