IL-6 promotes ICAM-1 expression and cell motility in human osteosarcoma

被引:59
作者
Lin, Yu-Min [2 ,3 ]
Chang, Zi-Ling [4 ]
Liao, Yuan-Ya [5 ]
Chou, Ming-Chih [2 ]
Tang, Chih-Hsin [1 ,4 ]
机构
[1] China Med Univ, Sch Med, Dept Pharmacol, Taichung, Taiwan
[2] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[3] Taichung Vet Gen Hosp, Dept Orthoped Surg, Taichung, Taiwan
[4] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Surg, Taichung, Taiwan
关键词
IL-6; IL-6R; ILK; Osteosarcoma; Migration; AUTOCRINE GROWTH-FACTOR; BREAST-CANCER CELLS; NF-KAPPA-B; IN-VITRO; GENE-EXPRESSION; SIGNALING PATHWAY; INTERLEUKIN-6; ADHESION; CARCINOMA; INTEGRIN;
D O I
10.1016/j.canlet.2012.08.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is characterized by a high malignant and metastatic potential. Interleukin-6 (IL-6) is a multifunctional cytokine that is associated with the disease status and outcomes of cancers. However, the effect of IL-6 on migration activity in human osteosarcoma cells is mostly unknown. Here we found that IL-6 increased the migration and expression of intercellular adhesion molecule-1 (ICAM-1) in human osteosarcoma cells. Transfection of cells with ICAM-1 siRNA reduced IL-6-mediated cell migration. We also found that expression of IL-6 was significantly greater in human osteosarcoma tissues than in normal bone. The integrin-linked kinase (ILK)/Akt/AP-1 pathway was activated after IL-6 treatment, and IL-6-induced expression of ICAM-1 and migration activity was inhibited by the specific inhibitor and siRNA of ILK, Akt, and AP-1 cascades. In addition, over-expression of IL-6 shRNA inhibited the migratory ability and ICAM-1 expression in osteosarcoma cells. Taken together, these results indicate that IL-6 and IL-6 receptor interaction occurs through ILK and Akt, which in turn activates AP-1, resulting in the activations of ICAM-1 and contributing the migration of human osteosarcoma cells. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:135 / 143
页数:9
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