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Conceptualization of fibroblast growth factor receptor 1 targeting nanomedicines
Yilin Ma1, Mengqin Guo2, Yang Liu3
1Program of Pharmacy, International School, Jinan University, Guangzhou 510632, Guangdong, China.
Abstract:
Fibroblast growth factor receptor 1 (FGFR1) is crucial in the progression of various cancers, participating in the processes of cell proliferation, survival, and differentiation. FGFR1 plays a role in the resistance to immune checkpoint inhibitors (ICIs) such as pembrolizumab and nivolumab. Therefore, using monoclonal antibodies and tyrosine kinase inhibitors to target FGFR1 and enhancing ICIs by modifying the tumor microenvironment and combating immune suppression represents a potential therapeutic strategy. Based on the FGFR1-related research and the active targeting strategy, we believe that modifying the surface of nanomedicines with anti-FGFR1 antibodies (such as OM-RCA-01) is an effective targeted treatment method for tumors with high expression of FGFR1. Although there have been relevant studies confirming the feasibility of this approach, there are challenges in clinical application, especially in terms of maintaining uniform quality during large-scale production. Therefore, we suggest conducting further optimization studies in the future to accelerate the clinical application of such drug delivery systems and provide more efficient and cost-effective options for tumor treatment.
Insights
Targeting Fibroblast Growth Factor Receptor 1 (FGFR1) with nanomedicines offers a promising strategy to overcome resistance to immune checkpoint inhibitors (ICIs) in cancer. Further optimization is needed for clinical translation of this targeted therapy.
Area of Science:
- Oncology
- Immunotherapy
- Nanomedicine
Background:
- Fibroblast Growth Factor Receptor 1 (FGFR1) is implicated in cancer progression, influencing cell proliferation, survival, and differentiation.
- FGFR1 signaling contributes to resistance against immune checkpoint inhibitors (ICIs) like pembrolizumab and nivolumab.
- Targeting FGFR1 presents a therapeutic avenue to enhance ICI efficacy by modulating the tumor microenvironment.
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