Specific blockade of the ERK pathway inhibits the invasiveness of tumor cells: down-regulation of matrix metalloproteinase-3/-9/-14 and CD44

被引:76
作者
Tanimura, S [1 ]
Asato, K [1 ]
Fujishiro, S [1 ]
Kohno, M [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Lab Cell Regulat, Dept Pharmaceut Sci, Nagasaki 8528521, Japan
关键词
tumor cells; invasiveness; ERK pathway; MEK inhibitor; matrix metalloproteinase; anti-metastatic effect;
D O I
10.1016/S0006-291X(03)00670-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elevated expression of matrix metalloproteinases (MMPs) is associated with increased metastatic potential in many tumor cells. As activation of the ERK pathway has been linked to the expression of MMP-9, we examined a possible correlation between ERK activation, MMP-9 expression, and invasive phenotype in human tumor cells. Activation state of the ERK pathway in tumor cells was well correlated with the invasive phenotype, which was determined by the ability of cells to invade through reconstituted extracellular matrix. Elevated expression of MMP-9 as well as of MMP-3, MMP-14, and CD44 was observed in tumor cells in which constitutive activation of the ERK pathway is detected. Blockade of the ERK pathway by treatment with PD184352, a specific and powerful inhibitor of mitogen-activated protein (MAP) kinase/ERK kinase (MEK), suppressed the expression of MMP-3, MMP-9, MMP-14. and CD44, and inhibited markedly the invasiveness of tumor cells. These results imply that, in addition to anti-proliferative effects, specific blockade of the ERK pathway is expected to result in anti-metastatic effects in tumor cells. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:801 / 806
页数:6
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