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沉默环状OMA1通过吸附miR-1294调控c-Myc表达来抑制骨肉瘤进展。

Silencing circOMA1 Inhibits Osteosarcoma Progression by Sponging miR-1294 to Regulate c-Myc Expression.

作者信息

Shi Yubo, Tian Yunyun, Sun Xiangran, Qiu Yonglong, Zhao Yingchun

机构信息

Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Front Oncol. 2022 Apr 13;12:889583. doi: 10.3389/fonc.2022.889583. eCollection 2022.

Abstract

BACKGROUND

Several studies have reported that circRNAs have a crucial function in the tumorigenesis of various cancers. However, the expression and function of circOMA1 in osteosarcoma is unknown.

METHODS

circOMA1 was identified through bioinformatics analysis. qRT-PCR was used to assess the expressions of circOMA1, miR-1294, and c-Myc in osteosarcoma tissues. Further, we performed functional experiments to explore the biological function of circOMA1 in osteosarcoma. Moreover, a luciferase reporter assay, RNA immunoprecipitation (RIP), and fluorescence hybridisation (FISH) assay were performed to demonstrate the association between circOMA1 and miR-1294.

RESULTS

circOMA1 exhibited considerable upregulation in osteosarcoma tissues compared with adjacent normal tissues. Silencing circOMA1 suppressed osteosarcoma progression and . Mechanically, circOMA1 functioned as a sponge of miR-1294 to upregulate c-Myc expression.

CONCLUSION

circOMA1 played the role of an oncogene in osteosarcoma and promoted osteosarcoma progression by mediating the miR-1294/c-Myc pathway, which might be a new target for treating osteosarcoma.

摘要

背景

多项研究报道环状RNA(circRNAs)在多种癌症的肿瘤发生过程中具有关键作用。然而,circOMA1在骨肉瘤中的表达及功能尚不清楚。

方法

通过生物信息学分析鉴定circOMA1。采用qRT-PCR检测circOMA1、miR-1294和c-Myc在骨肉瘤组织中的表达。此外,我们进行了功能实验以探究circOMA1在骨肉瘤中的生物学功能。而且,进行了荧光素酶报告基因检测、RNA免疫沉淀(RIP)和荧光原位杂交(FISH)实验以证明circOMA1与miR-1294之间的关联。

结果

与相邻正常组织相比,circOMA1在骨肉瘤组织中显著上调。沉默circOMA1可抑制骨肉瘤进展。机制上,circOMA1作为miR-1294的海绵发挥作用,上调c-Myc表达。

结论

circOMA1在骨肉瘤中发挥癌基因作用,并通过介导miR-1294/c-Myc通路促进骨肉瘤进展,这可能是治疗骨肉瘤的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5be2/9043560/58f80c478d76/fonc-12-889583-g001.jpg

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