Related Experiment Video
Updated: Feb 3, 2026

Screening and Identification of Small Peptides Targeting Fibroblast Growth Factor Receptor2 using a Phage Display Peptide Library
Published on: September 30, 2019
Fibroblast growth factor receptors as treatment targets in clinical oncology
1Department of Omics Network, National Cancer Center, 5-1-1 Tsukiji, Chuo ward, Tokyo, Japan. mkatoh-kkr@umin.ac.jp.
Abstract:
FGFRs are receptor tyrosine kinases with a role in several biological processes, such as the regulation of development and tissue repair. However, alterations in FGFRs 1-4, such as amplifications, fusions and mutations, as well as aberrant epigenetic or transcriptional regulation and changes in tumour-stromal interactions in the tumour microenvironment, can lead to the development and/or progression of cancer. Similar to other kinase alterations, such alterations are targetable using small molecules or antibodies, and the benefits of FGFR inhibitors have been demonstrated in clinical trials involving subsets of patients with solid tumours harbouring FGFR alterations. However, the response rates in patients with FGFR alterations were relatively low, and responses in patients without detectable FGFR alterations were also observed. In this Review, the author describes the clinical experience with FGFR inhibitors to date, and highlights key aspects that might lead to improved response rates and/or the avoidance of acquired resistance, including the selection of patients who are most likely to benefit from treatment, and the use of FGFR inhibitors in combination regimens with other agents.
Insights
Fibroblast Growth Factor Receptors (FGFRs) alterations drive cancer, but FGFR inhibitors show limited response rates. This review explores strategies to improve patient selection and combination therapies for better outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Fibroblast Growth Factor Receptors (FGFRs) are crucial for development and tissue repair.
- Aberrant FGFR signaling, through alterations like amplifications and mutations, contributes to cancer development and progression.
- FGFRs are implicated in various solid tumors, making them therapeutic targets.
Purpose of the Study:
- To review the clinical experience with FGFR inhibitors in cancer treatment.
- To identify key factors for improving response rates and overcoming resistance to FGFR inhibitors.
- To explore strategies for optimizing the use of FGFR inhibitors in clinical practice.
Main Methods:
- Review of clinical trial data and scientific literature on FGFR inhibitors.
- Analysis of patient populations with and without FGFR alterations.
- Evaluation of resistance mechanisms and combination therapy approaches.
Main Results:
- FGFR inhibitors have shown clinical benefits in subsets of patients with solid tumors harboring FGFR alterations.
- Response rates with FGFR inhibitors have been relatively low, with observed responses in patients lacking detectable FGFR alterations.
- Acquired resistance and limited efficacy highlight the need for refined treatment strategies.
Conclusions:
- Improved patient selection is critical to maximize benefit from FGFR inhibitors.
- Combination regimens involving FGFR inhibitors may enhance efficacy and overcome resistance.
- Further research is needed to fully elucidate the potential of FGFR-targeted therapies.
More Related Videos
12:36A Human Corneal Organ Culture Model of Descemet's Stripping Only with Accelerated Healing Stimulated by Engineered Fibroblast Growth Factor 1
Published on: July 22, 2022
09:16Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy
Published on: September 11, 2015
Related Concept Videos
Role of Hematopoietic Growth Factors
Thrombopoietin (TPO), mainly released by the liver,...
Factors Influencing Microbial Growth: pH
Factors Influencing Microbial Growth: Temperature
Factors Influencing Microbial Growth: Osmolarity
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...