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Cancer-Associated Fibroblasts Suppress Cancer Development: The Other Side of the Coin

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.613534

Keywords

cancer-associated fibroblasts; neoplasms; tumor microenvironment; biomarker; Humans

Funding

  1. Zhejiang Provincial Natural Science Foundation of China (Natural Science Foundation of Zhejiang Province) [LY20H180015]

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Cancer-associated fibroblasts (CAFs) are heterogeneous cells in the tumor microenvironment that can both promote and inhibit tumor development. The activation state of CAFs can vary, leading to different roles in early-stage and advanced-stage cancer. Understanding the diverse functions and origins of CAFs is crucial for developing precise cancer therapies.
Cancer-associated fibroblasts (CAFs) are the main stromal components of cancer, representing a group of heterogeneous cells. Many studies indicate that CAFs promote tumor development. Besides, evidence of the tumor suppression effects of CAFs keeps on merging. In the tumor microenvironment, multiple stimuli can activate fibroblasts. Notably, this does not necessarily mean the activated CAFs become strong tumor promoters immediately. The varying degree of CAFs activation makes quiescent CAFs, tumor-restraining CAFs, and tumor-promoting CAFs. Quiescent CAFs and tumor-restraining CAFs are more present in early-stage cancer, while comparatively, more tumor-promoting CAFs present in advanced-stage cancer. The underlying mechanism that balances tumor promotion or tumor inhibition effects of CAFs is mostly unknown. This review focus on the inhibitory effects of CAFs on cancer development. We describe the heterogeneous origin, markers, and metabolism in the CAFs population. Transgenetic mouse models that deplete CAFs or deplete CAFs activation signaling in the tumor stroma present direct evidence of CAFs protective effects against cancer. Moreover, we outline CAFs subpopulation and CAFs derived soluble factors that act as a tumor suppressor. Single-cell RNA-sequencing on CAFs population provides us new insight to classify CAFs subsets. Understanding the full picture of CAFs will help translate CAFs biology from bench to bedside and develop new strategies to improve precision cancer therapy.

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