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Long Non-Coding RNA CRNDE Promotes Colorectal Carcinoma Cell Progression and Paclitaxel Resistance by Regulating miR-126-5p/ATAD2 Axis

Authors :
Liu C
Hou J
Shan F
Wang L
Lu H
Ren T
Source :
OncoTargets and Therapy, Vol Volume 13, Pp 4931-4942 (2020)
Publication Year :
2020
Publisher :
Dove Medical Press, 2020.

Abstract

Chang Liu, Jianfeng Hou, Fengxiao Shan, Lijuan Wang, Hanjie Lu, Tiejun Ren Department of Oncology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang 471000, People’s Republic of ChinaCorrespondence: Chang Liu; Tiejun RenDepartment of Oncology, Luoyang Central Hospital Affiliated to Zhengzhou University, No. 288, Zhongzhou Road, Luoyang, Henan 471000, People’s Republic of ChinaEmail iqzxgf@163.com; gfwnhp@163.comBackground: Long non-coding RNA colorectal neoplasia differentially expressed (lncRNA CRNDE) and microRNA-126-5p (miR-126-5p) were reported to be related to the development of colorectal carcinoma (CRC). However, the detailed mechanism of CRNDE and miR-126-5p is not fully understood. The purpose of this research was to explore their roles and molecular mechanism in CRC.Methods: Quantitative real-time polymerase chain reaction was performed to detect the transcription levels of genes. Paclitaxel (PTX) was used to analyze cell drug resistance. 3-(4, 5-Dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay and flow cytometry analysis were employed to assess cell proliferation and apoptosis, respectively. Furthermore, cell migratory and invasive abilities were measured using transwell assay. The interaction between miR-126-5p and CRNDE or ATPase family AAA domain-containing protein 2 (ATAD2) was predicted by online tool starbase and then confirmed using the dual-luciferase reporter assay. Besides, Western blot assay was carried out to detect the levels of proteins.Results: CRNDE and ATAD2 expressions were upregulated and miR-126-5p expression was downregulated in CRC tissues and cells. CRNDE depletion repressed PTX resistance and the growth of CRC cells. Interestingly, we found that miR-126-5p was a target gene of CRNDE, and miR-126-5p directly targeted ATAD2. Furthermore, CRNDE affected CRC cell progression via modulation of miR-126-5p/ATAD2 axis in CRC cells.Conclusion: Our data suggested that CRNDE regulated CRC cell development and PTX resistance by modulating miR-126-5p/ATAD2 axis, providing the theoretical basis for the treatment of CRC patients.Keywords: CRNDE, miR-126-5p, ATAD2, PTX resistance, cell progression, colorectal carcinoma

Details

Language :
English
ISSN :
11786930
Database :
OpenAIRE
Journal :
OncoTargets and Therapy
Accession number :
edsair.doajarticles..df937a61651ddc819d48e293cce7a437