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Microenvironmental regulation in tumor progression: Interactions between cancer-associated fibroblasts and immune cells.
- Source :
-
Biomedicine & Pharmacotherapy . Nov2023, Vol. 167, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- The tumor microenvironment (TME), the "soil" on which tumor cells grow, has an important role in regulating the proliferation and metastasis of tumor cells as well as their response to treatment. Cancer-associated fibroblasts (CAFs), as the most abundant stromal cells of the TME, can not only directly alter the immunosuppressive effect of the TME through their own metabolism, but also influence the aggregation and function of immune cells by secreting a large number of cytokines and chemokines, reducing the body's immune surveillance of tumor cells and making them more prone to immune escape. Our study provides a comprehensive review of fibroblast chemotaxis, malignant transformation, metabolic characteristics, and interactions with immune cells. In addition, the current small molecule drugs targeting CAFs have been summarized, including both natural small molecules and targeted drugs for current clinical therapeutic applications. A complete review of the role of fibroblasts in TME from an immune perspective is presented, which has important implications in improving the efficiency of immunotherapy by targeting fibroblasts. [Display omitted] • Complex regulatory relationships between fibroblasts and immune cells during metabolism, chemotaxis, and malignant transformation. • Fibroblasts regulate immune cell activity in an environmentally dependent manner. • Natural small molecules targeting CAFs and targeted drugs for current clinical therapeutic applications. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CANCER invasiveness
*FIBROBLASTS
*CELL metabolism
*SMALL molecules
*STROMAL cells
Subjects
Details
- Language :
- English
- ISSN :
- 07533322
- Volume :
- 167
- Database :
- Academic Search Index
- Journal :
- Biomedicine & Pharmacotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 172976599
- Full Text :
- https://doi.org/10.1016/j.biopha.2023.115622