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撤回:miR-27b靶向HOXB8以抑制骨肉瘤的恶性行为。

RETRACTED: miR-27b Targets HOXB8 to Inhibit Malignant Behaviors of Osteosarcoma.

作者信息

Wu Yingyong, Peng Jinyun

机构信息

Orthopaedic Eight Disease Area, Mindong Hospital, Ningde, People's Republic of China.

Mindong Hospital, Ningde, People's Republic of China.

出版信息

Technol Cancer Res Treat. 2019 Jan-Dec;18:1533033819870791. doi: 10.1177/1533033819870791.

Abstract

MicroRNAs function as either tumor suppressor or oncogene in human cancers. This study aimed to explore the role of miR-27b in osteosarcoma. Expression of miR-27b or homeobox B8 in osteosarcoma cell lines was analyzed by quantitative real-time polymerase chain reaction and Western blot, respectively. Luciferase activity reporter assay and Western blot were conducted to explore the association between miR-27b and homeobox B8. Cell Counting Kit-8, colony formation assay, and wound-healing assay were performed to investigate the role of miR-27b or homeobox B8 on cell proliferation, colony formation, and cell migration. Expression of miR-27b was significantly reduced, while homeobox B8 was increased in osteosarcoma cell lines. In addition, homeobox B8 was validated as a direct target of homeobox B8. Moreover, miR-27b regulates osteosarcoma cell proliferation, colony formation, and migration through targeting homeobox B8. Taken together, our study provides novel insight into the progression of osteosarcoma, and the miR-27b–homeobox B8 axis identified may be developed as therapeutic targets against hepatocellular carcinoma in the future.

摘要

微小RNA在人类癌症中发挥着肿瘤抑制因子或癌基因的作用。本研究旨在探讨miR-27b在骨肉瘤中的作用。分别通过定量实时聚合酶链反应和蛋白质印迹法分析骨肉瘤细胞系中miR-27b或同源盒B8的表达。进行荧光素酶活性报告基因检测和蛋白质印迹法以探究miR-27b与同源盒B8之间的关联。采用细胞计数试剂盒-8、集落形成试验和伤口愈合试验来研究miR-27b或同源盒B8对细胞增殖、集落形成和细胞迁移的作用。在骨肉瘤细胞系中,miR-27b的表达显著降低,而同源盒B8的表达增加。此外,同源盒B8被证实为miR-27b的直接靶点。而且,miR-27b通过靶向同源盒B8来调节骨肉瘤细胞的增殖、集落形成和迁移。综上所述,我们的研究为骨肉瘤的进展提供了新的见解,并且所确定的miR-27b-同源盒B8轴未来可能被开发为针对骨肉瘤的治疗靶点。 (注:原文最后说针对肝癌治疗靶点有误,应是骨肉瘤)

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