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Updated: May 23, 2026

Cancer-Associated Fibroblasts from Mouse Mammary Tumors as Tools for Molecular and Computational Studies
Published on: July 3, 2025
Fibroblast growth factor receptors in breast cancer: expression, downstream effects, and possible drug targets
M Tenhagen1, P J van Diest, I A Ivanova
1Department of Pathology Division of Internal Medicine and Dermatology, University Medical Center Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands.
Abstract:
Cancer treatments are increasingly focusing on the molecular mechanisms underlying the oncogenic processes present in tumors of individual patients. Fibroblast growth factor receptors (FGFRs) are among the many molecules that are involved in oncogenesis and are currently under investigation for their potential as drug targets in breast cancer patients. These receptor tyrosine kinases play a role in several processes including proliferation, angiogenesis, and migration. Alterations in these basal processes can contribute to the development and progression of tumors. Among breast cancer patients, several subgroups have been shown to harbor genetic aberrations in FGFRs, including amplifications of FGFR1, FGFR2, and FGFR4 and mutations in FGFR2 and FGFR4. Here, we review in vitro and in vivo models that have partly elucidated the molecular implications of these different genetic aberrations, the resulting tumor characteristics, and the potential of FGFRs as therapeutic targets for breast cancer treatment.
Insights
Fibroblast growth factor receptors (FGFRs) are key in breast cancer development. Targeting FGFRs offers a promising therapeutic strategy for specific breast cancer patient subgroups with genetic aberrations.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cancer therapy increasingly targets individual patient tumor molecular mechanisms.
- Fibroblast growth factor receptors (FGFRs) are implicated in oncogenesis and are potential drug targets for breast cancer.
- FGFRs regulate critical cellular processes like proliferation, angiogenesis, and migration, which are often altered in tumors.
Purpose of the Study:
- To review in vitro and in vivo models that elucidate the molecular implications of genetic aberrations in FGFRs.
- To understand the resulting tumor characteristics associated with FGFR alterations.
- To assess the therapeutic potential of targeting FGFRs in breast cancer treatment.
Main Methods:
- Review of in vitro studies on FGFR genetic aberrations.
- Review of in vivo models investigating FGFRs in breast cancer.
- Analysis of molecular mechanisms and tumor characteristics linked to FGFR alterations.
Main Results:
- Genetic aberrations in FGFRs (amplifications and mutations) are present in specific breast cancer subgroups.
- These aberrations impact tumor proliferation, angiogenesis, and migration.
- In vitro and in vivo models have provided insights into the functional consequences of these genetic changes.
Conclusions:
- FGFRs represent a significant therapeutic target for breast cancer.
- Understanding FGFR genetic aberrations is crucial for developing targeted therapies.
- Targeting FGFRs may offer personalized treatment options for breast cancer patients with specific genetic alterations.
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