Open Access
Open access
volume 22 issue 1 publication number 60

Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment

Ruiwen Ruan 1, 2
Li Li 1, 2
Xuan Li 1, 2
Chunye Huang 1, 2
Zhanmin Zhang 1, 2
Hongguang Zhong 1, 2
Shaocheng Zeng 1, 2
Qianqian Shi 1, 2
Yang Xia 1, 2
Qinru Zeng 1, 2
Qin Wen 1, 2
Jingyi Chen 1, 2
Xiaofeng Dai 1, 2
JianPing Xiong 1, 2
Xiaojun Xiang 1, 2
Lei Wan 1, 2
Jun Deng 1, 2
Publication typeJournal Article
Publication date2023-03-25
scimago Q1
wos Q1
SJR9.263
CiteScore47.4
Impact factor33.9
ISSN14764598
Cancer Research
Oncology
Molecular Medicine
Abstract
Background

Fibroblast growth factors (FGFs) and their receptors (FGFRs) play a crucial role in cell fate and angiogenesis, with dysregulation of the signaling axis driving tumorigenesis. Therefore, many studies have targeted FGF/FGFR signaling for cancer therapy and several FGFR inhibitors have promising results in different tumors but treatment efficiency may still be improved. The clinical use of immune checkpoint blockade (ICB) has resulted in sustained remission for patients.

Main

Although there is limited data linking FGFR inhibitors and immunotherapy, preclinical research suggest that FGF/FGFR signaling is involved in regulating the tumor microenvironment (TME) including immune cells, vasculogenesis, and epithelial-mesenchymal transition (EMT). This raises the possibility that ICB in combination with FGFR-tyrosine kinase inhibitors (FGFR-TKIs) may be feasible for treatment option for patients with dysregulated FGF/FGFR signaling.

Conclusion

Here, we review the role of FGF/FGFR signaling in TME regulation and the potential mechanisms of FGFR-TKI in combination with ICB. In addition, we review clinical data surrounding ICB alone or in combination with FGFR-TKI for the treatment of FGFR-dysregulated tumors, highlighting that FGFR inhibitors may sensitize the response to ICB by impacting various stages of the “cancer-immune cycle”.

Found 
Found 

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GOST Copy
Ruan R. et al. Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment // Molecular Cancer. 2023. Vol. 22. No. 1. 60
GOST all authors (up to 50) Copy
Ruan R., Li L., Li X., Huang C., Zhang Z., Zhong H., Zeng S., Shi Q., Xia Y., Zeng Q., Wen Q., Chen J., Dai X., Xiong J., Xiang X., Lei Wan, Deng J. Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment // Molecular Cancer. 2023. Vol. 22. No. 1. 60
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1186/s12943-023-01761-7
UR - https://doi.org/10.1186/s12943-023-01761-7
TI - Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment
T2 - Molecular Cancer
AU - Ruan, Ruiwen
AU - Li, Li
AU - Li, Xuan
AU - Huang, Chunye
AU - Zhang, Zhanmin
AU - Zhong, Hongguang
AU - Zeng, Shaocheng
AU - Shi, Qianqian
AU - Xia, Yang
AU - Zeng, Qinru
AU - Wen, Qin
AU - Chen, Jingyi
AU - Dai, Xiaofeng
AU - Xiong, JianPing
AU - Xiang, Xiaojun
AU - Lei Wan
AU - Deng, Jun
PY - 2023
DA - 2023/03/25
PB - Springer Nature
IS - 1
VL - 22
PMID - 36966334
SN - 1476-4598
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2023_Ruan,
author = {Ruiwen Ruan and Li Li and Xuan Li and Chunye Huang and Zhanmin Zhang and Hongguang Zhong and Shaocheng Zeng and Qianqian Shi and Yang Xia and Qinru Zeng and Qin Wen and Jingyi Chen and Xiaofeng Dai and JianPing Xiong and Xiaojun Xiang and Lei Wan and Jun Deng},
title = {Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment},
journal = {Molecular Cancer},
year = {2023},
volume = {22},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1186/s12943-023-01761-7},
number = {1},
pages = {60},
doi = {10.1186/s12943-023-01761-7}
}