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靶向生存素基因的小干扰RNA抑制人肿瘤细胞生长。

Small interfering RNA targeting of the survivin gene inhibits human tumor cell growth .

作者信息

Zhang Zhaoxia, Wang Tianyou, Liu Ziqin, Tang Suoqin, Yue Mei, Feng Shunqiao, Hu Mengze, Xuan Litian, Chen Yanfei

机构信息

Department of Hematology and Oncology, Capital Institute of Pediatrics, Beijing 100020, P.R. China.

Department of Hematology and Oncology, Beijing Children's Hospital, Capital Medical University, Beijing 100045, P.R. China.

出版信息

Exp Ther Med. 2017 Jul;14(1):35-42. doi: 10.3892/etm.2017.4501. Epub 2017 May 23.

Abstract

The present study aimed to evaluate the impact of small interfering RNA (siRNA) targeting of the survivin gene in human tumor cells and the effect of decreased survivin expression on the proliferation and apoptosis of tumor cells. Human tumor cell lines (MSA-MB-231, SGC-7901, HeLa, A549, SK-OV-3 and Raji, PC-3) were cultured and divided into three groups: survivin siRNA-treated, scrambled negative control siRNA-treated and an untreated control group. The level of survivin mRNA and protein expression was subsequently determined by reverse transcription-quantitative polymerase chain reaction and western blot analysis, respectively. Cell proliferation was also examined by an MTT assay following transfection and the apoptotic rate of cells was detected by Hoechst and Annexin V/propidium iodide staining. It was observed that relative to the control group, expression of survivin mRNA and protein in the survivin siRNA-treated group was significantly downregulated. Furthermore, siRNA targeting of survivin lead to the inhibition of tumor cell proliferation, as well as an increase in their apoptotic rate . These data suggest that survivin may be a potential tumor biomarker and a novel target for the treatment of cancer.

摘要

本研究旨在评估靶向生存素基因的小干扰RNA(siRNA)对人肿瘤细胞的影响,以及生存素表达降低对肿瘤细胞增殖和凋亡的作用。培养人肿瘤细胞系(MSA-MB-231、SGC-7901、HeLa、A549、SK-OV-3和Raji、PC-3)并分为三组:生存素siRNA处理组、乱序阴性对照siRNA处理组和未处理对照组。随后分别通过逆转录定量聚合酶链反应和蛋白质印迹分析确定生存素mRNA和蛋白表达水平。转染后通过MTT法检测细胞增殖情况,并通过Hoechst和膜联蛋白V/碘化丙啶染色检测细胞凋亡率。结果观察到,相对于对照组,生存素siRNA处理组中生存素mRNA和蛋白的表达显著下调。此外,靶向生存素的siRNA导致肿瘤细胞增殖受到抑制,同时凋亡率增加。这些数据表明,生存素可能是一种潜在的肿瘤生物标志物,也是癌症治疗的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b9c/5488478/73ff8c292f23/etm-14-01-0035-g00.jpg

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