Fibulin-5 Suppresses Lung Cancer Invasion by Inhibiting Matrix Metalloproteinase-7 Expression

被引:90
作者
Yue, Wen
Sun, Quanhong [2 ]
Landreneau, Rodney [3 ]
Wu, Chuanyue [2 ]
Siegfried, Jill M.
Yu, Jian [2 ]
Zhang, Lin [1 ]
机构
[1] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Sch Med,Dept Pharmacol & Chem Biol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Inst Canc, Dept Pathol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Inst Canc, Dept Surg, Pittsburgh, PA 15213 USA
关键词
IN-VIVO; DOWN-REGULATION; GENES; CELLS; OVEREXPRESSION; PROGRESSION; METASTASIS; ELASTIN; PROLIFERATION; DETERMINANTS;
D O I
10.1158/0008-5472.CAN-09-0398
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The high mortality rate of lung cancer is largely due to the spread of disease to other organs. However, the molecular changes driving lung cancer invasion and metastasis remain unclear. In this study, we identified fibulin-5, a vascular ligand for integrin receptors, as a suppressor of lung cancer invasion and metastasis. Fibulin-5 was silenced by promoter hypermethylation in a majority of lung cancer cell lines and primary tumors. It inhibited lung cancer cell invasion and down-regulated matrix metalloproteinase-7 (MMP-7), which promoted lung cancer cell invasion. Knockdown of fibulin-5 was sufficient to stimulate cell invasion and MMP-7 expression. The expression levels of fibulin-5 and MMP-7 were inversely correlated in lung tumors. Suppression of MMP-7 expression by fibulin-5 was mediated by an integrin-binding RGD motif via the extracellular signal-regulated kinase (ERK) pathway. Furthermore, overexpression of fibulin-5 in H460 lung cancer cells inhibited metastasis in mice. Collectively, these results suggest that epigenetic silencing of fibulin-5 promotes lung cancer invasion and metastasis by activating MMP-7 expression through the ERK pathway. [Cancer Res 2009;69(15):6339-46]
引用
收藏
页码:6339 / 6346
页数:8
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