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微小RNA-26b通过靶向结缔组织生长因子(CTGF)和Smad1抑制骨肉瘤转移。

MicroRNA-26b inhibits metastasis of osteosarcoma via targeting CTGF and Smad1.

作者信息

Duan Guoqing, Ren Chunfeng, Zhang Yuanmin, Feng Shiqing

机构信息

Department of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.

出版信息

Tumour Biol. 2015 Aug;36(8):6201-9. doi: 10.1007/s13277-015-3305-6. Epub 2015 Mar 12.

Abstract

Downregulation of miR-26b has been found in various cancers, but it has never been investigated in osteosarcoma. In this study, we demonstrated downregulation of miR-26b in osteosarcoma tissues, negatively correlated with the expression of connective tissue growth factor (CTGF) and Smad1. Luciferase reporter assay confirmed the interaction of miR-26b with the 3' untranslated regions (UTRs) of CTGF and Smad1. Transfection of miR-26b in osteosarcoma cells suppressed the expression of CTGF and Smad1, suggesting CTGF and Smad1 as direct targets of miR-26b. Overexpression of miR-26b inhibited the migration of osteosarcoma cells, which was reversed by overexpression of CTGF or Smad1. Knockdown of CTGF by small interfering RNA (siRNA) interference blocked the activation of Smad1, ERK1/2, and MMP2, which was opposite to the overexpression of CTGF. Differently, Smad1 did not significantly affect CTGF level, but mediated ERK1/2 phosphorylation and MMP2 activation. Furthermore, miR-26b inhibited lung metastasis of osteosarcoma in vivo. Our data indicated that downregulation of miR-26b in osteosarcoma elevated the levels of CTGF and Smad1, facilitating osteosarcoma metastasis.

摘要

在多种癌症中均发现miR-26b表达下调,但在骨肉瘤中尚未有相关研究。在本研究中,我们证实了骨肉瘤组织中miR-26b表达下调,且与结缔组织生长因子(CTGF)和Smad1的表达呈负相关。荧光素酶报告基因检测证实了miR-26b与CTGF和Smad1的3'非翻译区(UTR)相互作用。在骨肉瘤细胞中转染miR-26b可抑制CTGF和Smad1的表达,提示CTGF和Smad1是miR-26b的直接靶点。miR-26b过表达抑制了骨肉瘤细胞的迁移,而CTGF或Smad1过表达可逆转这一作用。通过小干扰RNA(siRNA)干扰敲低CTGF可阻断Smad1、ERK1/2和MMP2的激活,这与CTGF过表达的作用相反。不同的是,Smad1对CTGF水平无显著影响,但可介导ERK1/2磷酸化和MMP2激活。此外,miR-26b在体内可抑制骨肉瘤的肺转移。我们的数据表明,骨肉瘤中miR-26b表达下调会升高CTGF和Smad1水平,促进骨肉瘤转移。

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