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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 receptor signaling as therapeutic targets in gastric cancer
Masakazu Yashiro1, Tasuku Matsuoka1
1Masakazu Yashiro, Tasuku Matsuoka, Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka 545-8585, Japan.
Abstract:
Fibroblast growth factor receptors (FGFRs) regulate a variety of cellular functions, from embryogenesis to adult tissue homeostasis. FGFR signaling also plays significant roles in the proliferation, invasion, and survival of several types of tumor cells. FGFR-induced alterations, including gene amplification, chromosomal translocation, and mutations, have been shown to be associated with the tumor initiation and progression of gastric cancer, especially in diffuse-type cancers. Therefore, the FGFR signaling pathway might be one of the therapeutic targets in gastric cancer. This review aims to provide an overview of the role of FGFR signaling in tumorigenesis, tumor progression, proliferation, and chemoresistance. We also discuss the accumulating evidence that demonstrates the effectiveness of using clinical therapeutic agents to inhibit FGFR signaling for the treatment of gastric cancer.
Insights
Fibroblast growth factor receptor (FGFR) signaling drives gastric cancer progression and chemoresistance. Inhibiting FGFR signaling with therapeutic agents shows promise for treating gastric cancer, particularly diffuse-type.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Fibroblast growth factor receptors (FGFRs) are crucial for normal cellular functions, including development and tissue maintenance.
- FGFR signaling is implicated in the growth, spread, and survival of various cancer cells.
- Alterations in FGFRs, such as mutations and amplifications, are linked to gastric cancer initiation and progression, especially in diffuse-type cancers.
Purpose of the Study:
- To review the role of FGFR signaling in gastric cancer development, progression, and treatment resistance.
- To explore FGFR signaling as a potential therapeutic target in gastric cancer.
- To summarize evidence supporting FGFR inhibition for gastric cancer therapy.
Main Methods:
- Literature review of studies on FGFR signaling in gastric cancer.
- Analysis of research on FGFR alterations and their impact on tumorigenesis.
- Examination of clinical data on FGFR-targeted therapies for gastric cancer.
Main Results:
- FGFR signaling pathways are significantly involved in gastric cancer cell proliferation, invasion, and survival.
- FGFR alterations are key drivers in the initiation and progression of gastric cancer.
- Evidence indicates that inhibiting FGFR signaling can be an effective therapeutic strategy.
Conclusions:
- The FGFR signaling pathway is a critical factor in gastric cancer pathogenesis.
- Targeting FGFR signaling represents a promising therapeutic avenue for gastric cancer treatment.
- Clinical agents inhibiting FGFR signaling demonstrate efficacy in preclinical and clinical settings for gastric cancer.
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