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Updated: Mar 30, 2026

Screening and Identification of Small Peptides Targeting Fibroblast Growth Factor Receptor2 using a Phage Display Peptide Library
Published on: September 30, 2019
Targeting fibroblast growth factor receptor (FGFR) pathway in renal cell carcinoma
Francesco Massari1, Chiara Ciccarese1, Matteo Santoni2
1a Medical Oncology , Azienda Ospedaliera Universitaria Integrata, University of Verona , Verona , Italy.
Abstract:
Fibroblast growth factor receptor (FGFR) pathway is involved in driving vascular endothelial growth factor (VEGF)-independent tumor angiogenesis, as a compensatory mechanism to escape VEGF-targeted therapies. Therefore, targeting FGF/FGFR axis seems to be a promising strategy in order to inhibit tumor angiogenesis and reduce resistance to VEGF receptor-tyrosine kinase inhibitors. This editorial is focused on the role of FGF/FGFR pathway in renal cell carcinoma and on the ongoing trials of emerging agents targeting this axis.
Insights
Targeting the Fibroblast Growth Factor (FGF)/FGF Receptor (FGFR) pathway may overcome resistance to VEGF-targeted therapies by inhibiting tumor angiogenesis. This approach shows promise for renal cell carcinoma treatment.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Tumor angiogenesis, crucial for cancer growth, can become independent of vascular endothelial growth factor (VEGF).
- The Fibroblast Growth Factor (FGF)/FGF Receptor (FGFR) pathway acts as a compensatory mechanism in VEGF-independent angiogenesis.
- This compensatory pathway contributes to resistance against VEGF-targeted therapies in various cancers.
Purpose of the Study:
- To review the role of the FGF/FGFR pathway in renal cell carcinoma (RCC) pathogenesis.
- To discuss the potential of targeting the FGF/FGFR axis to overcome resistance to VEGF-targeted therapies in RCC.
- To highlight ongoing clinical trials investigating novel agents targeting the FGF/FGFR pathway in RCC.
Main Methods:
- Literature review of preclinical and clinical studies.
- Analysis of the molecular mechanisms underlying FGF/FGFR signaling in RCC.
- Summary of ongoing clinical trials for FGF/FGFR inhibitors in RCC.
Main Results:
- The FGF/FGFR pathway is implicated in driving VEGF-independent tumor angiogenesis in RCC.
- Inhibition of the FGF/FGFR axis demonstrates potential in sensitizing tumors to VEGF-targeted therapies.
- Emerging agents targeting FGF/FGFR are under investigation in various phases of clinical trials for RCC.
Conclusions:
- Targeting the FGF/FGFR pathway represents a promising strategy to combat tumor angiogenesis and resistance in RCC.
- Further research and clinical trials are warranted to establish the efficacy of FGF/FGFR-targeted agents in RCC treatment.
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