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miR-1826表达下调提示骨肉瘤患者预后不良,并调控肿瘤细胞增殖、迁移和侵袭。

Downregulation of miR-1826 Indicates a Poor Prognosis for Osteosarcoma Patients and Regulates Tumor Cell Proliferation, Migration, and Invasion.

作者信息

Li Peng, Wei Lei, Zhu Wenshuai

机构信息

Department of Spine Orthopaedics, Weifang Traditional Chinese Hospital, Weifang, Shandong 261041, China.

Department of Spinal Surgery, Weifang People's Hospital, Weifang, Shandong 261041, China.

出版信息

Int J Genomics. 2020 Feb 11;2020:7968407. doi: 10.1155/2020/7968407. eCollection 2020.

Abstract

BACKGROUND

Osteosarcoma (OS) is the most frequent bone tumor with high metastasis. This study is aimed at assessing the expression and prognostic significance of microRNA-1826 (miR-1826) in OS patients, as well as its biological function in tumor progression.

METHODS

Quantitative Real-Time PCR was employed to measure the expression of miR-1826 in OS tissues and cell lines. Kaplan-Meier survival analysis and Cox regression model were used to evaluate the prognostic value of miR-1826. CCK-8 and Transwell assay were conducted to investigate the effect of miR-1826 on OS cell proliferation, migration, and invasion.

RESULTS

miR-1826 expression was downregulated in OS tissues and cell lines and associated with OS patients' clinical stage and distant metastasis. Low levels of miR-1826 were related with shorter survival time and determined as an independent prognostic indicator for the overall survival of OS patients. The overexpression of miR-1826 in OS cells led to inhibited cell proliferation, migration, and invasion.

CONCLUSION

The decreased expression of miR-1826 predicts a poor prognosis in OS patients, and its overexpression inhibits OS cell proliferation, migration, and invasion. This newly identified miR-1826 provides a novel sight into the pathogenesis of OS and offers a candidate prognostic biomarker and therapeutic target for OS treatment.

摘要

背景

骨肉瘤(OS)是最常见的具有高转移率的骨肿瘤。本研究旨在评估微小RNA-1826(miR-1826)在骨肉瘤患者中的表达及预后意义,以及其在肿瘤进展中的生物学功能。

方法

采用定量实时聚合酶链反应(qRT-PCR)检测骨肉瘤组织和细胞系中miR-1826的表达。采用Kaplan-Meier生存分析和Cox回归模型评估miR-1826的预后价值。进行CCK-8和Transwell实验以研究miR-1826对骨肉瘤细胞增殖、迁移和侵袭的影响。

结果

miR-1826在骨肉瘤组织和细胞系中的表达下调,且与骨肉瘤患者的临床分期和远处转移相关。低水平的miR-1826与较短的生存时间相关,并被确定为骨肉瘤患者总生存的独立预后指标。miR-1826在骨肉瘤细胞中的过表达导致细胞增殖、迁移和侵袭受到抑制。

结论

miR-1826表达降低预示骨肉瘤患者预后不良,其过表达抑制骨肉瘤细胞增殖、迁移和侵袭。新发现的miR-1826为骨肉瘤的发病机制提供了新的视角,并为骨肉瘤治疗提供了一个候选的预后生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f57/7036115/dac91ba5f3e3/IJG2020-7968407.001.jpg

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