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CircRNA CDR1as/miR-7 signals promote tumor growth of osteosarcoma with a potential therapeutic and diagnostic value 期刊论文

编号：

2f3fd124-3e71-485a-a4cb-2544da7a143c
作者：

Xu, Bo#^[1]Yang, Tieyi^[1];Wang, Zhi#^[1]Zhang, Yan^[1];Liu, Shuyi^[1];Shen, Mingquan*^[2]
语种：

英文
期刊：

CANCER MANAGEMENT AND RESEARCH ISSN：1179-1322 2018 年 10 卷 (4871 - 4880)
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关键词：

CDR1as miR-7 osteosarcoma apoptosis EMT
摘要：

Background: The circular RNA (circRNA) antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as)/micro RNA-7(miR-7) signal axis has been investigated in many diseases via regulation of the target genes of miR-7, which participates in the carcinogenesis and metastasis. However, the clinical role and function of CDR1as/miR-7 pathway in osteosarcoma (OS) remain to be identified.
Materials and methods: Noncancerous bone tissues (n=18) and OS tissues (n=38) were used to determine the expressions and roles of CDR1as and miR-7. We knocked down the expression of CDR1as via siRNAs in OS cell lines to analyze its function in vitro and in vivo.
Results: CDR1as was upregulated in OS tissues with significant diagnostic value (cutoff value: 1.613). OS patients with high tumor size, Enneking stage, and distant metastasis have high CDR1as levels, but the miR-7 as tumor suppressor negatively correlated with CDR1as. Inhibition of CDR1as in OS cell lines U2OS and MG63 with high CDR1as levels, leading to derepressed miR-7 levels, impaired cell vitality and increased apoptosis and G1/S arrest in parallel with reduced ability of cell migration, which, however, could be restored by miR-7 inhibitor. Mechanistically, knockdown of CDR1as could restore the availability of miR-7 and inhibit the target genes of miR-7 including EGFR, CCNE1, PI3KCD, and RAF1. Moreover, CDR1as also upregulated N-cadherin and inhibited E-cadherin to promote the epithelial-mesenchymal transition via miR-7 for cell migration. CDR1as inhibition in vivo also induced tumor regression with decreased PCNA levels, and miR-7 inhibitor could reverse these effects via upregulation of EGFR, CCNE1, PI3KCD, and RAF1. The expressions of these genes were confirmed to be higher in CDR1as-high OS samples than in CDR1as-low OS samples.
Conclusion: These findings suggested that the CDR1as/miR-7 signal axis could be the molecular target for the treatment of OS.
推荐引用方式
GB/T 7714：

Xu Bo,Yang Tieyi,Wang Zhi, et al. CircRNA CDR1as/miR-7 signals promote tumor growth of osteosarcoma with a potential therapeutic and diagnostic value [J].CANCER MANAGEMENT AND RESEARCH,2018,10:4871-4880.
APA：

Xu Bo,Yang Tieyi,Wang Zhi,Zhang Yan,&Shen Mingquan.(2018).CircRNA CDR1as/miR-7 signals promote tumor growth of osteosarcoma with a potential therapeutic and diagnostic value .CANCER MANAGEMENT AND RESEARCH,10:4871-4880.
MLA：

Xu Bo, et al. "CircRNA CDR1as/miR-7 signals promote tumor growth of osteosarcoma with a potential therapeutic and diagnostic value" .CANCER MANAGEMENT AND RESEARCH 10(2018):4871-4880.
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