Tumor‐derived EMMPRIN (extracellular matrix metalloproteinase inducer) stimulates collagenase transcription through MAPK p38

FEBS Letters

Basbaum, Carol³  Cameron, Robert²  Guo, Huiming¹  Jablons, David²  Toole, Bryan¹  Martinez, Tom³  Li, Jian-dong³  Lim, Melissa³ 

[1] Department of Cell Biology, Tufts University School of Medicine, Boston, MA 02116, USA;Department of Thoracic Surgery, University of California, San Francisco, San Francisco, CA 94143-0452, USA;Department of Anatomy, University of California, San Francisco, San Francisco, CA 94143-0452, USA

关键词: Extracellular matrix metalloproteinase inducer;    Metalloproteinase;    MAP kinase;    p38;    Matrix metalloproteinase-1;   

DOI  :  10.1016/S0014-5793(98)01474-4

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

EMMPRIN (extracellular matrix metalloproteinase inducer) stimulates fibroblast metalloproteinases (MMP) 1, 2 and 3 (Kataoka et al. (1993) Cancer Res. 53, 3154–3158). Here we focus on MMP-1, showing that in lung tumors, MMP-1's cognate mRNA is strongly expressed in stromal fibroblasts adjacent to EMMPRIN-expressing tumor cells. In vitro, EMMPRIN upregulates MMP-1 mRNA expression in a concentration-dependent manner, with a peak accumulation at 24 h. The response is genistein-sensitive, suggesting it is dependent on tyrosine kinase activity. Analysis of tyrosine phosphorylation-dependent MAP kinases ERK 1/2, SAPK/JNK, and p38 showed that the activity of p38 but not that of the other 2 kinases was elevated in response to EMMPRIN. That p38 activity was required for EMMPRIN stimulation of MMP-1 was evident from results showing that the p38 inhibitor SB203580 blocked this response. This is the first available information regarding the mechanism by which tumor-associated molecules upregulate MMP synthesis in stromal fibroblasts.

【 授权许可】

Unknown