Interleukin-6 induces vascular endothelial growth factor expression and promotes angiogenesis through apoptosis signal-regulating kinase 1 in human osteosarcoma

被引:95
作者
Tzeng, Huey-En [1 ,2 ]
Tsai, Chun-Hao [1 ,3 ]
Chang, Zi-Ling [4 ]
Su, Chen-Ming [4 ]
Wang, Shih-Wei [5 ]
Hwang, Wen-Li [2 ]
Tang, Chih-Hsin [4 ,6 ]
机构
[1] China Med Univ, Grad Inst Clin Med Sci, Taichung, Taiwan
[2] Taichung Vet Gen Hosp, Div Hematol Oncol, Taichung, Taiwan
[3] China Med Univ Hosp, Dept Orthopaed Surg, Taichung, Taiwan
[4] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[5] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[6] China Med Univ, Dept Pharmacol, Sch Med, Taichung, Taiwan
关键词
IL-6; VEGF; ASK1; Angiogenesis; Osteosarcoma; IN-VITRO; CELL-LINES; TUMOR ANGIOGENESIS; IL-6; FUNCTIONS; CARCINOMA; ACTIVATION; RECEPTOR; PATHWAY; CANCER; GENE;
D O I
10.1016/j.bcp.2012.11.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Osteosarcoma is characterized by a high malignant and metastatic potential. Angiogenesis is essential for the caner metastasis. Interleukin-6 (IL-6) is a multifunctional cytokine that is associated with the disease status and outcomes of cancers. However, the relationship between IL-6 and vascular endothelial growth factor (VEGF) expression in human osteosarcoma is mostly unknown. Here we found that the IL-6 and VEGF expression was correlated with tumor stage and significantly higher than that in normal bone. Incubation of osteosarcoma cells with IL-6 increased VEGF mRNA and protein expression. Pretreatment of cells with IL-6R antibody reduced IL-6-mediated VEGF production. The apoptosis signal-regulating kinase 1 (ASK1)/p38/AP-1 pathway was activated after IL-6 treatment, and IL-6-induced VEGF expression was abolished by the specific inhibitor and siRNA of ASK1, p38, and AP-1 cascades. Importantly, knockdown IL-6 reduced VEGF expression and abolished osteosarcoma conditional medium-mediated angiogenesis. Taken together, these results indicate that IL-6 occurs through ASK1 and p38, which in turn activates AP-1, resulting in the activations of VEGF expression and contributing the angiogenesis of human osteosarcoma cells. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:531 / 540
页数:10
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