Amphiregulin enhances intercellular adhesion molecule-1 expression and promotes tumor metastasis in human osteosarcoma

被引:25
|
作者
Liu, Ju-Fang [1 ]
Tsao, Ya-Ting [2 ]
Hou, Chun-Han [2 ]
机构
[1] Shin Kong Wu Ho Su Mem Hosp, Cent Lab, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Orthoped Surg, Taipei, Taiwan
关键词
amphiregulin; osteosarcoma metastasis; cell migration; ICAM-1; EGFR; EPIDERMAL-GROWTH-FACTOR; CANCER CELL-MIGRATION; REGULATING KINASE 1; ALPHA TGF-ALPHA; ICAM-1; EXPRESSION; FACTOR RECEPTOR; AUTOCRINE GROWTH; DUCTAL MORPHOGENESIS; INTEGRIN EXPRESSION; SIGNALING PATHWAY;
D O I
10.18632/oncotarget.5679
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is a common, high malignant, and metastatic bone cancer. Amphiregulin (AREG) has been associated with cancer cellular activities. However, the effect of AREG on metastasis activity in human osteosarcoma cells has yet to be determined. We determined that AREG increases the expression of intercellular adhesion molecule-1 (ICAM-1) through PI3K/Akt signaling pathway via its interaction with the epidermal growth factor receptor, thus resulting in the enhanced cell migration of osteosarcoma. Furthermore, AREG stimulation increased the association of NF-kappa B to ICAM-1 promoter which then up-regulated ICAM-1 expression. Finally, we observed that shRNA silencing of AREG decreased osteosarcoma metastasis in vivo. Our findings revealed a relationship between osteosarcoma metastatic potential and AREG expression and the modulating effect of AREG on ICAM-1 expression.
引用
收藏
页码:40880 / 40895
页数:16
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