Epithelial carcinogenesis: dynamic interplay between neoplastic cells and their microenvironment

被引:65
作者
van Kempen, LCL
Rhee, JS
Dehne, K
Lee, J
Edwards, DR
Coussens, LM
机构
[1] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94115 USA
[2] Univ Calif San Francisco, Med Sci Training Program, San Francisco, CA 94143 USA
[3] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[4] Univ Calif San Francisco, Dept Pathol, San Francisco, CA USA
[5] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
cancer; inflammation; matrix metalloproteinase; angiogenesis; transgenic mice;
D O I
10.1046/j.1432-0436.2002.700914.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Matrix metalloproteinases (MMPs) have long been thought of as critical factors regulating matrix degradation associated with cell invasion into ectopic tissue compartments during primary tumor growth and metastasis. One member of the MMP family historically linked to these invasive processes is MMP-9/gelatinase B. By studying a transgenic mouse model of de novo epithelial carcinogenesis, new roles for MMP-9 have emerged that broaden the view of its functional contribution to malignant progression. The combined implication of these studies suggest that MMP-9 functionally contributes to cancer development; however, its major regulatory role may be in its ability to activate poorly diffusible and/or matrix-sequestered growth factors that regulate epithelial and/or endothelial cell growth as opposed to regulating cellular invasion across basement membranes.
引用
收藏
页码:610 / 623
页数:14
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