Polo-like kinase 1 siRNA-607 induces mitotic arrest and apoptosis in human nasopharyngeal carcinoma cells

被引:0
作者
Zhu, Jiang [1 ]
Lan, Huan [2 ,3 ]
Hong, Suling [1 ]
Hu, Guohua [1 ]
Ai, Qing [2 ,3 ]
Yang, Zhengmei [2 ]
Ke, Xia [1 ]
Song, Fangzhou [2 ,3 ]
Bu, Youquan [2 ,3 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R China
[3] Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
Nasopharyngeal carcinoma; Plk1; RNA silencing; cell cycle; apoptosis; CANCER-CELLS; PLK1; INHIBITION; ACTIVATION; EXPRESSION; INDUCTION; DEPLETION; MITOSIS; GROWTH; (PLK)1;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Polo-like kinase (Plk) 1 is overexpressed in many human malignancies including nasopharyngeal carcinoma, indicating its potential as a therapeutic target. Recently, using a simple cellular morphology-based strategy, we have identified several novel effective siRNAs against Plk1 including Plk1 siRNA-607. In this study, we further investigated the effects of Plk1 siRNA-607 in human nasopharyngeal carcinoma cell line, HNE-1. Real time RT-PCR and Western blot indicated that Plk1 siRNA-607 transfection resulted in a significant inhibition in Plk1 expression in the HNE-1 cells. Furthermore, cell cycle, cell growth and apoptosis analysis clearly indicated that Plk1 siRNA-607 caused a dramatic mitotic cell cycle arrest followed by massive apoptotic cell death, and eventually resulted in a significant decrease in growth and viability of the nasopharyngeal carcinoma cells. Given that Plk1 has been widely accepted as a novel efficient target for cancer therapy, these results suggested that Plk1 siRNA-607 could be further developed for the treatment of human nasopharyngeal carcinoma.
引用
收藏
页码:6809 / 6815
页数:7
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