Upregulation of circ_0000142 promotes multiple myeloma progression by adsorbing miR-610 and upregulating AKT3 expression

被引:26
|
作者
Liu, Fang [1 ]
Wang, Yan-Li [1 ]
Wei, Jie-Mei [1 ]
Huang, Zhao-Dong [2 ]
机构
[1] Linyi Cent Hosp, Dept Hematol, 17 Hlth Rd, Linyi 276400, Shandong, Peoples R China
[2] Linyi Cent Hosp, Dept Intervent, 17 Hlth Rd, Linyi 276400, Shandong, Peoples R China
关键词
AKT3; ceRNA; circ_0000142; miR-610; MM; PROLIFERATION; BIOMARKER; CANCER; RNA;
D O I
10.1093/jb/mvaa106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular RNAs (circRNAs) play an important regulatory role in a variety of malignancies. Nevertheless, the role of circ_0000142 in multiple myeloma (MM) and its regulatory mechanism remains largely unknown. Real-time polymerase chain reaction was employed to detect the expressions of circ_0000142 and miR-610 in MM tissues and cell lines. The expression of AKT3 and apoptosis-related proteins (Bcl2, Bax) in MM cells was detected by western blot. The correlation between the expression level of circ_0000142 and the clinicopathological parameters of MM patients was analysed. Cell proliferation, apoptosis, migration and invasion were monitored by Cell Counting Kit 8 assay, flow cytometry analysis and Transwell assay, respectively. The dual-luciferase reporter gene assay and RNA immunoprecipitation assay were employed to verify the targeting relationship between circ_0000142 and miR-610. In this study, it was demonstrated that, circ_0000142 was highly expressed in MM patients, and its high expression level was significantly associated with increased International Staging System and Durk- Salmon stage. Overexpression of circ_0000142 enhanced MM cell proliferation, migration, invasion and suppressed cell apoptosis, while knocking down circ_0000142 had the opposite effects. Mechanistically, circ_0000142 functioned as a competitive endogenous RNA, directly targeting miR-610 and positively regulating AKT3 expression. In brief, circ_0000142 enhances the proliferation and metastasis of MM cells by modulating the miR-610/AKT3 axis.
引用
收藏
页码:327 / 336
页数:10
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