Cancer associated fibroblasts and metabolic reprogramming: unraveling the intricate crosstalk in tumor evolution

被引:0
|
作者
Zhang, Fusheng [1 ]
Ma, Yongsu [1 ]
Li, Dongqi [1 ]
Wei, Jianlei [2 ,3 ]
Chen, Kai [1 ]
Zhang, Enkui [1 ]
Liu, Guangnian [1 ]
Chu, Xiangyu [1 ]
Liu, Xinxin [1 ]
Liu, Weikang [1 ]
Tian, Xiaodong [1 ]
Yang, Yinmo [1 ]
机构
[1] Peking Univ First Hosp, Dept Hepatobiliary & Pancreat Surg, Beijing 100034, Peoples R China
[2] Jiamusi Univ, Sch Basic Med, Key Lab Microecol Immune Regulatory Network & Rela, Jiamusi 154007, Heilongjiang, Peoples R China
[3] Peking Univ, Key Lab Carcinogenesis & Translat Res, Dept Biochem & Mol Biol, Sch Basic Med Sci,Hlth Sci Ctr, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
Cancer-associated fibroblasts; Metabolic reprogramming; Immune suppression; Inflammatory microenvironment; Tumor metastasis; Tumor therapy; CARCINOMA-ASSOCIATED FIBROBLASTS; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER; ACTIVATION PROTEIN; GASTRIC-CANCER; TGF-BETA; BONE METASTASIS; RECIPROCAL INTERACTIONS; IMMUNE SUPPRESSION; COLORECTAL-CANCER;
D O I
10.1186/s13045-024-01600-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metabolic reprogramming provides tumors with an energy source and biofuel to support their survival in the malignant microenvironment. Extensive research into the intrinsic oncogenic mechanisms of the tumor microenvironment (TME) has established that cancer-associated fibroblast (CAFs) and metabolic reprogramming regulates tumor progression through numerous biological activities, including tumor immunosuppression, chronic inflammation, and ecological niche remodeling. Specifically, immunosuppressive TME formation is promoted and mediators released via CAFs and multiple immune cells that collectively support chronic inflammation, thereby inducing pre-metastatic ecological niche formation, and ultimately driving a vicious cycle of tumor proliferation and metastasis. This review comprehensively explores the process of CAFs and metabolic regulation of the dynamic evolution of tumor-adapted TME, with particular focus on the mechanisms by which CAFs promote the formation of an immunosuppressive microenvironment and support metastasis. Existing findings confirm that multiple components of the TME act cooperatively to accelerate the progression of tumor events. The potential applications and challenges of targeted therapies based on CAFs in the clinical setting are further discussed in the context of advancing research related to CAFs.
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页数:32
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