Fibroblast diversity and plasticity in the tumor microenvironment: roles in immunity and relevant therapies

被引:0
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作者
Yashi Xu
Wei Li
Shitong Lin
Binghan Liu
Peng Wu
Li Li
机构
[1] Union Hospital,Department of Obstetrics and Gynecology
[2] Tongji Medical College,Cancer Biology Research Center (Key Laboratory of the Ministry of Education)
[3] Huazhong University of Science and Technology,National Clinical Research Center for Gynecology and Obstetrics
[4] Tongji Hospital,Department of Gynecologic Oncology
[5] Tongji Medical College,undefined
[6] Huazhong University of Science and Technology,undefined
[7] Tongji Hospital,undefined
[8] Tongji Medical College,undefined
[9] Huazhong University of Science and Technology,undefined
[10] Tongji Hospital,undefined
[11] Tongji Medical College,undefined
[12] Huazhong University of Science and Technology,undefined
关键词
Cancer-associated fibroblasts; Heterogeneity; Plasticity; Targeted therapies; Immunotherapies;
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学科分类号
摘要
Cancer-associated fibroblasts (CAFs), enriched in the tumor stroma, have received increasing attention because of their multifaceted effects on tumorigenesis, development, metastasis, and treatment resistance in malignancies. CAFs contributed to suppressive microenvironment via different mechanisms, while CAFs also exerted some antitumor effects. Therefore, CAFs have been considered promising therapeutic targets for their remarkable roles in malignant tumors. However, patients with malignancies failed to benefit from current CAFs-targeted drugs in many clinical trials, which suggests that further in-depth investigation into CAFs is necessary. Here, we summarize and outline the heterogeneity and plasticity of CAFs mainly by exploring their origin and activation, highlighting the regulation of CAFs in the tumor microenvironment during tumor evolution, as well as the critical roles performed by CAFs in tumor immunity. In addition, we summarize the current immunotherapies targeting CAFs, and conclude with a brief overview of some prospects for the future of CAFs research in the end.
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