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环状 RNA circ_0000337 通过 miR-4458/BACH1 通路促进骨肉瘤的发生。

Circular RNA circ_0000337 contributes to osteosarcoma via the miR-4458/BACH1 pathway.

机构信息

Department of Orthopaedics, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Department of Research and Teaching Department, Hanzhong Central Hospital, Hanzhong, Shaanxi, China.

出版信息

Cancer Biomark. 2020;28(4):411-419. doi: 10.3233/CBM-190647.

Abstract

BACKGROUND

As the most prevalent primary bone malignancy in children and adolescents, osteosarcoma (OS) has attracted increasing attention. The role of circRNAs in OS has been elucidated in some reports, but many circRNAs remain unexplored. Circ_0000337 has only been revealed as an oncogenic circRNA in esophageal squamous cell carcinoma. Yet whether circ_0000337 exerts any specific function in OS has not been unmasked.

METHODS

RT-qPCR was used for measurement of circ_0000337, miR-4458 and BACH1 mRNA levels. Western blot was conducted to detect BACH1 protein. CCK-8 assay, Casepase-3 activity assay and transwell assay were utilized to assess changes on cellular processes. Cytoplasmic/nuclear fractionation assay was conducted for circ_0000337 localization in OS cells. Luciferase reporter assay and RIP assay were performed to validate the interaction between miR-4458 and circ_0000337 or BACH1.

RESULTS

Circ_0000337 expression was upregulated in OS cell lines and it silence hindered OS cell proliferation and migration. MiR-4458 was downregulated in OS cells and miR-4458 upregulation suppressed OS cell growth and migration. Importantly, circ_0000337 sponged miR-4458 to elevate BACH1 expression, thus facilitating OS development.

CONCLUSIONS

This research for the first time documented that circ_0000337 promoted OS progression via sponging miR-4458 and thus elevating BACH1 expression, offering rational therapeutic target for OS.

摘要

背景

骨肉瘤(OS)作为儿童和青少年中最常见的原发性骨恶性肿瘤,引起了越来越多的关注。CircRNAs 在 OS 中的作用在一些报道中已经阐明,但许多 CircRNAs 仍未被探索。Circ_0000337 仅在食管鳞状细胞癌中被揭示为致癌 CircRNA。然而,Circ_0000337 是否在 OS 中发挥任何特定功能尚未被揭示。

方法

使用 RT-qPCR 测量 circ_0000337、miR-4458 和 BACH1 mRNA 水平。Western blot 用于检测 BACH1 蛋白。CCK-8 测定、Caspase-3 活性测定和 Transwell 测定用于评估细胞过程的变化。细胞质/核分馏测定用于 OS 细胞中 circ_0000337 的定位。荧光素酶报告基因测定和 RIP 测定用于验证 miR-4458 与 circ_0000337 或 BACH1 之间的相互作用。

结果

Circ_0000337 在 OS 细胞系中表达上调,其沉默抑制 OS 细胞增殖和迁移。MiR-4458 在 OS 细胞中下调,miR-4458 的上调抑制 OS 细胞的生长和迁移。重要的是,circ_0000337 通过海绵吸附 miR-4458 来升高 BACH1 表达,从而促进 OS 的发展。

结论

这项研究首次记录了 circ_0000337 通过海绵吸附 miR-4458 来促进 OS 进展,从而升高 BACH1 表达,为 OS 提供了合理的治疗靶点。

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