The extracellular matrix: A dynamic niche in cancer progression

被引:2552
作者
Lu, Pengfei [1 ,2 ,4 ,5 ,6 ]
Weaver, Valerie M. [3 ]
Werb, Zena [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dev & Stem Cell Biol Grad Program, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Ctr Bioengn & Tissue Regenerat, Dept Surg, San Francisco, CA 94143 USA
[4] Univ Manchester, Breakthrough Breast Canc Res Unit, Manchester M20 4BX, Lancs, England
[5] Univ Manchester, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
[6] Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Fac Life Sci, Manchester M20 4BX, Lancs, England
基金
美国国家卫生研究院;
关键词
STEM-CELL NICHE; LYSYL OXIDASE; STEM/PROGENITOR CELLS; LEUKOCYTE MIGRATION; STROMAL FIBROBLASTS; GENE-EXPRESSION; SELF-RENEWAL; IV COLLAGEN; IN-VIVO; ANGIOGENESIS;
D O I
10.1083/jcb.201102147
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The local microenvironment, or niche, of a cancer cell plays important roles in cancer development. A major component of the niche is the extracellular matrix (ECM), a complex network of macromolecules with distinctive physical, biochemical, and biomechanical properties. Although tightly controlled during embryonic development and organ homeostasis, the ECM is commonly deregulated and becomes disorganized in diseases such as cancer. Abnormal ECM affects cancer progression by directly promoting cellular transformation and metastasis. Importantly, however, ECM anomalies also deregulate behavior of stromal cells, facilitate tumor-associated angiogenesis and inflammation, and thus lead to generation of a tumorigenic microenvironment. Understanding how ECM composition and topography are maintained and how their deregulation influences cancer progression may help develop new therapeutic interventions by targeting the tumor niche.
引用
收藏
页码:395 / 406
页数:12
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