Remodeling and homeostasis of the extracellular matrix: implications for fibrotic diseases and cancer

被引:1251
作者
Cox, Thomas R. [1 ]
Erler, Janine T. [1 ]
机构
[1] Inst Canc Res, Canc Res UK Tumour Cell Signalling Unit, Sect Cell & Mol Biol, London SW3 6JB, England
关键词
GLYCATION END-PRODUCTS; TISSUE GROWTH-FACTOR; COAGULATION FACTOR-XIIIA; MAMMARY EPITHELIAL-CELL; LYSYL OXIDASE ACTIVITY; PHASE-I TRIAL; BREAST-CANCER; TGF-BETA; ENDOTHELIAL-CELLS; CONTRAST AGENT;
D O I
10.1242/dmm.004077
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
Dynamic remodeling of the extracellular matrix (ECM) is essential for development, wound healing and normal organ homeostasis. Life-threatening pathological conditions arise when ECM remodeling becomes excessive or uncontrolled. In this Perspective, we focus on how ECM remodeling contributes to fibrotic diseases and cancer, which both present challenging obstacles with respect to clinical treatment, to illustrate the importance and complexity of cell-ECM interactions in the pathogenesis of these conditions. Fibrotic diseases, which include pulmonary fibrosis, systemic sclerosis, liver cirrhosis and cardiovascular disease, account for over 45% of deaths in the developed world. ECM remodeling is also crucial for tumor malignancy and metastatic progression, which ultimately cause over 90% of deaths from cancer. Here, we discuss current methodologies and models for understanding and quantifying the impact of environmental cues provided by the ECM on disease progression, and how improving our understanding of ECM remodeling in these pathological conditions is crucial for uncovering novel therapeutic targets and treatment strategies. This can only be achieved through the use of appropriate in vitro and in vivo models to mimic disease, and with technologies that enable accurate monitoring, imaging and quantification of the ECM.
引用
收藏
页码:165 / 178
页数:14
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