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The FGF/FGFR System in Breast Cancer: Oncogenic Features and Therapeutic Perspectives
Maria Francesca Santolla1, Marcello Maggiolini1
1Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Abstract:
One of the major challenges in the treatment of breast cancer is the heterogeneous nature of the disease. With multiple subtypes of breast cancer identified, there is an unmet clinical need for the development of therapies particularly for the less tractable subtypes. Several transduction mechanisms are involved in the progression of breast cancer, therefore making the assessment of the molecular landscape that characterizes each patient intricate. Over the last decade, numerous studies have focused on the development of tyrosine kinase inhibitors (TKIs) to target the main pathways dysregulated in breast cancer, however their effectiveness is often limited either by resistance to treatments or the appearance of adverse effects. In this context, the fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) system represents an emerging transduction pathway and therapeutic target to be fully investigated among the diverse anti-cancer settings in breast cancer. Here, we have recapitulated previous studies dealing with FGFR molecular aberrations, such as the gene amplification, point mutations, and chromosomal translocations that occur in breast cancer. Furthermore, alterations in the FGF/FGFR signaling across the different subtypes of breast cancer have been described. Next, we discussed the functional interplay between the FGF/FGFR axis and important components of the breast tumor microenvironment. Lastly, we pointed out the therapeutic usefulness of FGF/FGFR inhibitors, as revealed by preclinical and clinical models of breast cancer.
Insights
Fibroblast growth factor receptor (FGFR) alterations are implicated in various breast cancer subtypes. FGFR inhibitors show promise as targeted therapies, addressing unmet needs in difficult-to-treat breast cancers.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Breast cancer exhibits significant heterogeneity, necessitating targeted therapies for diverse subtypes.
- Current treatments like tyrosine kinase inhibitors (TKIs) face limitations due to resistance and adverse effects.
- The fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) pathway is an emerging target in cancer.
Purpose of the Study:
- To review molecular aberrations in FGFR within breast cancer.
- To describe FGF/FGFR signaling alterations across breast cancer subtypes.
- To explore the therapeutic potential of FGF/FGFR inhibitors.
Main Methods:
- Literature review of studies on FGFR molecular aberrations (amplification, mutations, translocations).
- Analysis of FGF/FGFR signaling alterations in different breast cancer subtypes.
- Discussion of the interplay between FGF/FGFR axis and the tumor microenvironment.
- Evaluation of preclinical and clinical data on FGF/FGFR inhibitors.
Main Results:
- FGFR gene amplification, point mutations, and chromosomal translocations are recurrent in breast cancer.
- Altered FGF/FGFR signaling is observed across various breast cancer subtypes.
- The FGF/FGFR axis interacts with key components of the breast tumor microenvironment.
Conclusions:
- FGFR aberrations represent a significant therapeutic target in breast cancer.
- FGF/FGFR inhibitors demonstrate therapeutic utility in preclinical and clinical settings.
- Targeting the FGF/FGFR pathway offers a promising strategy for challenging breast cancer subtypes.
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