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A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
Targeting fibroblast growth factor pathways in endometrial cancer
Boris Winterhoff1, Gottfried E Konecny2
1Department of Obstetrics and Gynecology, University of Minnesota, Minneapolis, Minnesota.
Abstract:
Novel treatments that improve outcomes for patients with recurrent or metastatic endometrial cancer (EC) remain an unmet need. Aberrant signaling by fibroblast growth factors (FGFs) and FGF receptors (FGFRs) has been implicated in several human cancers. Activating mutations in FGFR2 have been found in up to 16% of ECs, suggesting an opportunity for targeted therapy. This review summarizes the role of the FGF pathway in angiogenesis and EC, and provides an overview of FGFR-targeted therapies under clinical development for the treatment of EC.
Insights
Novel treatments are needed for recurrent or metastatic endometrial cancer (EC). Fibroblast growth factor receptor (FGFR) mutations in EC present a target for new therapies, with several FGFR-targeted drugs in development.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Endometrial cancer (EC) with recurrence or metastasis lacks effective treatments.
- Fibroblast growth factor (FGF) and FGF receptor (FGFR) signaling is crucial in various cancers.
- Activating FGFR2 mutations occur in up to 16% of endometrial cancers.
Purpose of the Study:
- To review the role of the FGF pathway in angiogenesis and EC.
- To provide an overview of FGFR-targeted therapies for EC.
Main Methods:
- Literature review of the FGF pathway in EC.
- Summary of clinical development of FGFR-targeted therapies.
Main Results:
- The FGF pathway plays a significant role in angiogenesis and EC progression.
- FGFR-targeted therapies show promise for EC treatment.
Conclusions:
- Targeting FGFR2 mutations is a viable therapeutic strategy for EC.
- FGFR-targeted therapies are advancing in clinical development for EC.
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