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顺铂通过上调U-2OS骨肉瘤细胞中的Wrap53诱导细胞凋亡。

Cisplatin induces apoptosis via upregulating Wrap53 in U-2OS osteosarcoma cells.

作者信息

Yuan Jian-Min, Li Xue-Dong, Liu Zhao-Yong, Hou Guo-Qing, Kang Jian-Hui, Huang Dong-Yang, Du Shi-Xin

机构信息

Department of Orthopedics, the First Affiliated Hospital, China.

出版信息

Asian Pac J Cancer Prev. 2011;12(12):3465-9.

Abstract

Wrap531α, a newly identified natural antisense transcript of p53, can regulate p53 expression upon DNA damage. We sought to investigate changes in Wrap53 and p53 levels in an osteosarcoma cell line (U-2OS) exposed to cisplatin and to study apoptosis before and after knockdown of Wrap53. Our RT-PCR analysis showed a dose- dependent 3 to 40-fold increase in Wrap53 mRNA transcript levels in U-2OS exposed to 5 to 20 μM cisplatin. An approximate 2-fold increase was also observed in transcript levels of p53 mRNA. Furthermore, transient knockdown of Wrap53 by siRNAs in U-2OS cells treated with 10 μM cisplatin reduced p53 mRNA transcript levels by up to 50% of those of controls. Immunoblotting analysis showed that in U-2OS cells treated with siRNA against exon 4 of the Wrap53 gene, the protein level of p53 was also markedly reduced. Our findings suggest that cisplatin upregulates the expression of p53 in osteosarcoma cells by upregulating the transcript levels of Wrap53. Finally, measurement of apoptotic cell death by flow cytometry showed that knockdown of Wrap53 reduced apotosis in U-2OS cells induced by cisplatin.

摘要

Wrap53α是一种新发现的p53天然反义转录本,在DNA损伤时可调节p53表达。我们试图研究顺铂处理的骨肉瘤细胞系(U-2OS)中Wrap53和p53水平的变化,并研究Wrap53敲低前后的细胞凋亡情况。我们的逆转录聚合酶链反应(RT-PCR)分析显示,在暴露于5至20μM顺铂的U-2OS细胞中,Wrap53 mRNA转录水平呈剂量依赖性增加3至40倍。p53 mRNA转录水平也观察到约2倍的增加。此外,在用10μM顺铂处理的U-2OS细胞中,通过小干扰RNA(siRNA)瞬时敲低Wrap53可使p53 mRNA转录水平降低至对照的50%以下。免疫印迹分析表明,在用针对Wrap53基因第4外显子的siRNA处理的U-2OS细胞中,p53的蛋白水平也显著降低。我们的研究结果表明,顺铂通过上调Wrap53的转录水平来上调骨肉瘤细胞中p53的表达。最后,通过流式细胞术测量凋亡细胞死亡情况显示,敲低Wrap53可减少顺铂诱导的U-2OS细胞凋亡。

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