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miR-541 可作为骨肉瘤的预后生物标志物,通过靶向 TGIF2 调控骨肉瘤细胞的增殖、迁移和侵袭。

miR-541 serves as a prognostic biomarker of osteosarcoma and its regulatory effect on tumor cell proliferation, migration and invasion by targeting TGIF2.

机构信息

Department of Spinal Surgery, Weifang People's Hospital, No. 151 Guangwen Street, Weifang, 261000, Shandong, China.

出版信息

Diagn Pathol. 2020 Jul 24;15(1):96. doi: 10.1186/s13000-020-01008-9.

Abstract

BACKGROUND

Several studies reported the dysregulation of miR-541 in the progression of some human malignancies. Osteosarcoma (OS) is one of the most common primary malignant bone tumors. This study aimed to assess the expression and clinical significance of miR-541 in OS patients and explore the biological function of miR-541 in tumor progression.

METHODS

Expression of miR-541 was detected by quantitative real-time PCR, and its prognostic value was evaluated using Kaplan-Meier survival analysis. The biological function of miR-541 was examined by analyzing its effects on OS cell proliferation, migration and invasion. Additionally, the underlying potential target of miR-541 was predicated and analyzed.

RESULTS

The expression of miR-541 was significantly decreased in OS tissues and cell lines. The deregulated expression of miR-541 in tumor tissues was associated with the overall survival of OS patients and was a potential independent prognostic indicator. In OS cells, the overexpression of miR-541 could inhibit cell proliferation, migration and invasion. The luciferase activity results indicated that TGIF2 was a potential target of miR-541.

CONCLUSION

The results of this study revealed that the decreased miR-541 expression in OS patients may serve as a prognostic biomarker, and that the overexpression of miR-541 in OS cells results in inhibited cell proliferation, migration and invasion, indicating the potential of miR-541 as a therapeutic target in OS treatment.

摘要

背景

多项研究报告称,miR-541 在一些人类恶性肿瘤的进展中失调。骨肉瘤(OS)是最常见的原发性恶性骨肿瘤之一。本研究旨在评估 miR-541 在 OS 患者中的表达及其临床意义,并探讨 miR-541 在肿瘤进展中的生物学功能。

方法

通过定量实时 PCR 检测 miR-541 的表达,并通过 Kaplan-Meier 生存分析评估其预后价值。通过分析 miR-541 对 OS 细胞增殖、迁移和侵袭的影响来研究 miR-541 的生物学功能。此外,还预测并分析了 miR-541 的潜在潜在靶标。

结果

miR-541 的表达在 OS 组织和细胞系中明显降低。肿瘤组织中 miR-541 的失调表达与 OS 患者的总生存期相关,是一个潜在的独立预后指标。在 OS 细胞中,miR-541 的过表达可抑制细胞增殖、迁移和侵袭。荧光素酶活性结果表明,TGIF2 是 miR-541 的潜在靶标。

结论

本研究结果表明,OS 患者中 miR-541 的表达降低可能作为一种预后生物标志物,OS 细胞中 miR-541 的过表达导致细胞增殖、迁移和侵袭受到抑制,表明 miR-541 作为 OS 治疗的潜在治疗靶点的潜力。

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