5′-nitro-indirubinoxime induces G2/M cell cycle arrest and apoptosis in human KB oral carcinoma cells

被引:26
作者
Kim, Soo-A [2 ]
Kim, Si-Wouk [3 ]
Chang, Sunghoe [4 ]
Yoon, Jung-Hoon [1 ]
Ahn, Sang-Gun [1 ]
机构
[1] Chosun Univ, Coll Dent, Dept Pathol, Kwangju 501759, South Korea
[2] Dongguk Univ, Coll Oriental Med, Dept Biochem, Gyeongju 780714, South Korea
[3] Chosun Univ, Coll Engn, Dept Environm Engn, Kwangju 501759, South Korea
[4] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 501759, South Korea
关键词
Indirubin; 5 '-nitro-indirubinoxime; Cell cycle; PLK1; Apoptosis; INDIRUBIN DERIVATIVES; KINASE; PHOSPHORYLATION; INHIBITION; ACTIVATION; MECHANISMS; MEDICINE; PROPHASE; PROTEIN; MITOSIS;
D O I
10.1016/j.canlet.2008.08.033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
our previous study demonstrated that the novel indirubin derivative, 5'-nitro-indirubinoxime (5'-NIO), effectively at-rested the tumor growth through the inhibition of cell proliferation and the induction of apoptosis. However, the precise molecular mechanisms underlying 5'-NIO-induced antitumor activity remain unclear. Here, we report that 5'-NIO inhibits the proliferation of human KB oral carcinoma cells via the cell cycle arrest in G2/M phase. 5'-NIO reduced the activity of Cdc2/cyclin B complex through the inhibition of the PLK1 expression. Partially, 5'-NIO also arrested cell cycle in G1/S phase via the reduction of CDK4 and cyclin D1/D3 levels by p16 and induction of the level of p21(waf1). Using flow cytometry analysis, we showed that 5'-NIO-induced cell cycle arrest is followed by apoptosis. We determined further that 5'-NIO-induced apoptosis is accomplished by the mitochondira-dependent activation of the caspase cascade. Overall, these observations suggest the potential value of 5'-NIO as a candidate for a therapeutic modality for the treatment of oral cancer. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:72 / 77
页数:6
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