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真核生物翻译起始因子3H的抑制可抑制骨肉瘤细胞生长和肿瘤发生。

Eukaryotic translation initiation factor 3H suppression inhibits osteocarcinoma cell growth and tumorigenesis.

作者信息

Hong Song, Liu Yi, Xiong Huazhang, Cai Dongfeng, Fan Qinghong

机构信息

Department of Orthopedics, Affiliated Hospital of Zunyi Medical College, Zunyi, Guizhou 563003, P.R. China.

出版信息

Exp Ther Med. 2018 Jun;15(6):4925-4931. doi: 10.3892/etm.2018.6031. Epub 2018 Apr 3.

Abstract

Eukaryotic translation initiation factor 3H subunit (EIF3H) is a member of the EIF3 family and exhibits a central role in translation initiation in higher eukaryotes. Although EIF3H expression is upregulated in numerous tumour types, its potential role in human osteosarcoma (OS) has not yet been investigated. In the present study, it was demonstrated that mRNA expression was upregulated in the human OS cell lines Saos-2 and U2OS. A recombinant lentivirus harbouring short hairpin RNA targeting was constructed and successfully infected human OS Saos-2 and U2OS cells, resulting in 95% downregulated expression compared with the respective control groups. Knockdown of significantly inhibited the proliferation and colony formation of OS cells , and tumour growth in nude mice . Flow cytometry analysis revealed cell cycle arrest and promotion of apoptosis in OS cells with knocked down. In conclusion, the results strongly suggested that EIF3H is a critical factor mediating the growth of OS cells and may represent a novel therapeutic target.

摘要

真核生物翻译起始因子3H亚基(EIF3H)是EIF3家族的成员,在高等真核生物的翻译起始中发挥核心作用。尽管EIF3H在多种肿瘤类型中表达上调,但其在人类骨肉瘤(OS)中的潜在作用尚未得到研究。在本研究中,结果表明在人骨肉瘤细胞系Saos-2和U2OS中mRNA表达上调。构建了携带靶向短发夹RNA的重组慢病毒,并成功感染了人骨肉瘤Saos-2和U2OS细胞,与各自的对照组相比,导致EIF3H表达下调了95%。敲低EIF3H显著抑制了骨肉瘤细胞的增殖和集落形成,以及裸鼠体内的肿瘤生长。流式细胞术分析显示,敲低EIF3H的骨肉瘤细胞出现细胞周期阻滞并促进凋亡。总之,结果强烈表明EIF3H是介导骨肉瘤细胞生长的关键因子,可能代表一种新的治疗靶点。

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