Inhibition of cyclooxygenase-2-dependent survivin mediates decursin-induced apoptosis in human KBM-5 myeloid leukemia cells

被引:32
作者
Ahn, Quein [1 ]
Jeong, Soo-Jin [1 ]
Lee, Hyo-Jung [1 ]
Kwon, Hee-Young [1 ]
Han, Ihn [1 ]
Kim, Hyun Seok [2 ]
Lee, Hyo-Jeong [1 ]
Lee, Eun-Ok [1 ]
Ahn, Kwang Seok [1 ]
Jung, Min-Hyung [3 ]
Zhu, Shudong [4 ]
Chen, Chang-Yan [4 ]
Kim, Sung-Hoon [1 ]
机构
[1] Kyung Hee Univ, Coll Oriental Med, Seoul 130701, South Korea
[2] Yonsei Univ, Sch Med, Seoul 120752, South Korea
[3] Kyung Hee Univ, Sch Med, Seoul 130701, South Korea
[4] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
Decursin; Apoptosis; COX; 2; Survivin; KBM; 5; ANGELICA-GIGAS; TARGETING SURVIVIN; PROSTATE-CANCER; THERAPY; EXPRESSION; COX-2; ERYTHROLEUKEMIA; RESISTANCE; CARCINOMA; CASCADE;
D O I
10.1016/j.canlet.2010.07.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We demonstrate that decursin induces apoptosis via regulation of cyclooxygenase-2 (COX-2) and survivin in leukemic KBM-5 cells By activating an apoptotic machinery decursin is cytotoxic to KBM-5 cells In this apoptotic process decursin can activate caspase family members and triggers PARP cleavage At the same time the expression of COX-2 and survivin in the cells is downregulated Furthermore decursin is in synergy with COX-2 inhibitor celecoxib or NS398 for the induction of apoptosis Overall these results suggest that decursin via inhibiting COX-2 and survivin sensitizes human leukemia cells to apoptosis and is a potential chemotherapeutic agent to treat this disease (C) 2010 Elsevier Ireland Ltd All rights reserved
引用
收藏
页码:212 / 221
页数:10
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