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Microenvironmental regulation in tumor progression: Interactions between cancer-associated fibroblasts and immune cells.

Authors :
Gao, Dandan
Fang, Liguang
Liu, Cun
Yang, Mengrui
Yu, Xiaoyun
Wang, Longyun
Zhang, Wenfeng
Sun, Changgang
Zhuang, Jing
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]

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