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靶向细胞周期蛋白E1的miR-132抑制骨肉瘤细胞的增殖。

miR-132 targeting cyclin E1 suppresses cell proliferation in osteosarcoma cells.

作者信息

Wang Jin, Xu Guoxing, Shen Feng, Kang Yifan

机构信息

Department of Orthopedics, Changhai Hospital, Second Military Medical University, 168 Changhai Road, Shanghai, 200433, China.

出版信息

Tumour Biol. 2014 May;35(5):4859-65. doi: 10.1007/s13277-014-1637-2. Epub 2014 Jan 22.

Abstract

In this study, we investigated the roles of miR-132 in tumor growth of osteosarcoma. We found that overexpression of miR-132 significantly suppressed in vitro cell proliferation and in vivo tumor growth. In addition, miR-132 overexpression induced G1/S cell cycle arrest of osteosarcoma cells. Further study showed that miR-132 could interact with the 3'-untranslated region of cyclin E1 (CCNE1) gene and repress its expression. Re-expression of CCNE1 (without the 3'UTR) could partially abrogate the miR-132-induced cell proliferation inhibition. Of significance, contrary to CCNE1, expression level of miR-132 was significantly lower in osteosarcoma tissues than in the adjacent normal tissues. Taken together, these results indicate that miR-132 functions as a tumor suppressor in osteosarcoma and that its suppressive effects are mediated chiefly by repressing CCNE1 expression.

摘要

在本研究中,我们调查了miR-132在骨肉瘤肿瘤生长中的作用。我们发现,miR-132的过表达显著抑制体外细胞增殖和体内肿瘤生长。此外,miR-132过表达诱导骨肉瘤细胞的G1/S期细胞周期阻滞。进一步研究表明,miR-132可与细胞周期蛋白E1(CCNE1)基因的3'非翻译区相互作用并抑制其表达。CCNE1(无3'UTR)的重新表达可部分消除miR-132诱导的细胞增殖抑制。重要的是,与CCNE1相反,miR-132在骨肉瘤组织中的表达水平显著低于相邻正常组织。综上所述,这些结果表明miR-132在骨肉瘤中起肿瘤抑制作用,其抑制作用主要通过抑制CCNE1表达来介导。

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