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靶向E2F-1基因的短发夹RNA在体外抑制胃癌进展

Short interfering RNA directed against the E2F-1 gene suppressing gastric cancer progression in vitro.

作者信息

Xie Yubo, Yin Yongshuo, Li Lei, Ma Yulin, Xiao Qiang

机构信息

Department of Surgery, The First Affiliated Hospital, Guangxi Medical University, Guangxi 530021, PR China.

出版信息

Oncol Rep. 2009 May;21(5):1345-53. doi: 10.3892/or_00000360.

Abstract

Gastric cancer is the third most common cancer in China. The sustained overexpression of E2F-1 is a characteristic feature of gastric cancer. RNA interference (RNAi), which has been proven to be a powerful tool for suppressing gene expression, may provide a promising way forward in gastric cancer therapy. In this study, we constructed the recombinant Psilencer 4.1- E2F-1 siRNA plasmids and transfected them into gastric cancer MGC-803 cells in vitro. Our data demonstrated that E2F-1 siRNA led to inhibition of endogenous E2F-1 mRNA and protein expression as determined by real-time quantitative RT-PCR and Western blotting. Furthermore, simultaneous silencing of E2F-1 resulted in a reduction of tumor cell proliferation activity and a higher percentage of apoptotic cells. The inhibition of migration and invasion potential of tumor cells was investigated in vitro. In summary, siRNA targeting of E2F-1 can effectively inhibit gastric cancer progression and may be used as a potent therapy.

摘要

胃癌是中国第三大常见癌症。E2F-1的持续过表达是胃癌的一个特征。RNA干扰(RNAi)已被证明是抑制基因表达的有力工具,可能为胃癌治疗提供一条有前景的途径。在本研究中,我们构建了重组Psilencer 4.1-E2F-1 siRNA质粒,并在体外将其转染到胃癌MGC-803细胞中。我们的数据表明,通过实时定量RT-PCR和蛋白质免疫印迹法测定,E2F-1 siRNA导致内源性E2F-1 mRNA和蛋白质表达受到抑制。此外,同时沉默E2F-1导致肿瘤细胞增殖活性降低和凋亡细胞百分比升高。在体外研究了对肿瘤细胞迁移和侵袭潜能的抑制作用。总之,靶向E2F-1的siRNA可有效抑制胃癌进展,可能用作一种有效的治疗方法。

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