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Updated: May 5, 2026

A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
Cytokines and cancer-associated fibroblasts
Yidu Hu1, Jiaqi Liang1, Lewei Duan1
1Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, No. 180 Feng Lin Road Xuhui District, Shanghai, 200032, P.R. China.
Cancer-associated fibroblasts (CAFs) drive malignancy via cytokine signaling. This review categorizes cytokines and explores therapeutic strategies targeting CAF-mediated tumor progression and the tumor microenvironment (TME).
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- Cancer-associated fibroblasts (CAFs) are key stromal cells in the tumor microenvironment (TME).
- Cytokines mediate complex cell-to-cell communication, influencing tumor progression and immune responses within the TME.
- Understanding cytokine networks is crucial for developing effective cancer therapies.
Purpose of the Study:
- To systematically review and categorize cytokines involved in CAF-mediated tumor malignancy.
- To delineate the distinct roles of various cytokine families in CAF-tumor cell-immune cell interactions.
- To evaluate current and future therapeutic strategies targeting cytokine signaling in cancer.
Main Methods:
- Systematic review and categorization of cytokines based on their families (interleukins, chemokines, growth factors, etc.).
- Analysis of cytokine roles as upstream signals for CAF activation and as downstream effectors secreted by CAFs.
- Evaluation of therapeutic approaches targeting CAF functions and cytokine networks.
Main Results:
- Cytokines are fundamental mediators of CAF activation, tumor cell malignancy, and TME reprogramming.
- Specific cytokine families play distinct roles in the reciprocal interactions within the TME.
- Targeting cytokine networks offers potential therapeutic avenues, including CAF reprogramming and targeted delivery.
Conclusions:
- Cytokine signaling networks are critical regulators of CAF function and tumor progression.
- Targeting these networks presents promising therapeutic opportunities but faces challenges like pleiotropy and heterogeneity.
- A theoretical framework is needed to optimize cytokine-targeted therapies for precision oncology.
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