Hsa_circ_0001480 affects osteosarcoma progression by regulating the miR-363-3p/IBSP pathway

被引:0
|
作者
Bi, Guijuan [1 ]
Zhang, Li [1 ,2 ]
机构
[1] Wuhan Fourth Hosp, Dept Rehabil Med, Wuhan, Hubei, Peoples R China
[2] Wuhan Fourth Hosp, Dept Rehabil Med, 473 Hanzheng St, Wuhan 430000, Hubei, Peoples R China
关键词
circ_0001480; IBSP; miR-363-3p; osteosarcoma; CIRCULAR RNAS; PROLIFERATION; METASTASIS; EPIDEMIOLOGY; SURVIVAL; INVASION;
D O I
10.1002/bab.2571
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
Osteosarcoma (OS) is a malignant bone tumor that commonly affects young individuals. Circular RNAs (circRNAs) are associated with OS progression. In this study, we aimed to determine the role of hsa_circ_0001480 (circ_0001480) in OS development. OS cell invasion, viability, and colony numbers were assessed via transwell, cell counting kit-8, and colony formation assays, respectively. Tumor growth in vivo was also assessed using an OS mouse model. Additionally, targeted associations among the integrin-binding sialoprotein (IBSP), microRNA (miR)-363-3p, and circ_0001480 were evaluated via RNA immunoprecipitation and dual luciferase reporter assays, whereas their expression levels in OS cells and tissues were determined via quantitative reverse transcription-polymerase chain reaction and western blotting. Loss of circ_0001480 or IBSP significantly inhibited the proliferation and invasion of OS cells, but this effect was reversed by miR-363-3p downregulation. Moreover, circ_0001480 knockdown inhibited neoplasm growth in vivo. circ_0001480 directly bound to miR-363-3p, which further modulated IBSP. Both circ_0001480 and IBSP levels were high, whereas miR-363-3p levels were low in OS cells. Furthermore, low miR-363-3p levels attenuated the suppressive effects of circ_0001480 silencing on the proliferation and invasion of OS cells; however, loss of IBSP partially reversed these effects. Overall, our findings revealed circ_0001480 an oncogenic circRNA stimulating OS progression by modulating the miR-363-3p/IBSP pathway, suggesting its potential for OS treatment.
引用
收藏
页码:721 / 732
页数:12
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