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Cancer-Associated Fibroblasts Build and Secure the Tumor Microenvironment

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2019.00060

Keywords

cancer-associated fibroblast; tumor microenvironment; extracellular matrix; therapy; mechanoreciprocity

Funding

  1. CCTST Pilot Translational Research & Innovative Core Grant
  2. NIH [R15CA228014]

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Tumor cells reside in a highly complex and heterogeneous tumor microenvironment (TME), which is composed of a myriad of genetically stable non-cancer cells, including fibroblasts, immune cells, endothelial cells, and epithelial cells, and a tumor-specific extracellular matrix (ECM). Cancer-associated fibroblasts (CAFs), as an abundant and active stromal cell population in the TME, function as the signaling center and remodeling machine to aid the creation of a desmoplastic tumor niche. Although there is no denial that the TME and CAFs may have anti-tumor effects as well, a great deal of findings reported in recent years have convincingly revealed the tumor-promoting effects of CAFs and CAF-derived ECM proteins, enzymes, chemical factors and other downstream effectors. While there is growing enthusiasm for the development of CAF-targeting therapies, a better understanding of the complexities of CAF-ECM and CAF-cancer cell interactions is necessary before novel therapeutic strategies targeting the malignant tumor soil can be successfully implemented in the clinic.

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