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Updated: Jun 7, 2026

Experimental Generation of Carcinoma-Associated Fibroblasts (CAFs) from Human Mammary Fibroblasts
Published on: October 25, 2011
Roles of fibroblast growth factor receptors in carcinogenesis
Ellen Margrethe Haugsten1, Antoni Wiedlocha, Sjur Olsnes
1Department of Biochemistry, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0310 Oslo, Norway. Ellen.M.Haugsten@rr-research.no
Abstract:
The fibroblast growth factor receptors (FGFR) play essential roles both during development and in the adult. Upon ligand binding, FGFRs induce intracellular signaling networks that tightly regulate key biological processes, such as cell proliferation, survival, migration, and differentiation. Deregulation of FGFR signaling can thus alter tissue homeostasis and has been associated with several developmental syndromes as well as with many types of cancer. In human cancer, FGFRs have been found to be deregulated by multiple mechanisms, including aberrant expression, mutations, chromosomal rearrangements, and amplifications. In this review, we will give an overview of the main FGFR alterations described in human cancer to date and discuss their contribution to cancer progression.
Insights
Fibroblast growth factor receptors (FGFR) are crucial for cell regulation. Aberrant FGFR signaling drives cancer progression through various genetic alterations, impacting tissue homeostasis.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Fibroblast growth factor receptors (FGFR) are vital for development and adult tissue homeostasis.
- FGFR signaling regulates critical cellular functions including proliferation, survival, migration, and differentiation.
- Dysregulation of FGFR signaling is linked to developmental disorders and numerous cancers.
Purpose of the Study:
- To provide a comprehensive overview of FGFR alterations in human cancer.
- To discuss the mechanisms by which FGFR deregulation contributes to cancer progression.
Main Methods:
- Literature review of studies on FGFR alterations in human cancer.
- Analysis of mechanisms including aberrant expression, mutations, chromosomal rearrangements, and amplifications.
- Discussion of the functional impact of these alterations on cancer biology.
Main Results:
- FGFRs are frequently deregulated in human cancers through diverse genetic and epigenetic mechanisms.
- Specific FGFR alterations are associated with various cancer types and stages.
- These alterations can activate oncogenic signaling pathways, promoting tumor growth and metastasis.
Conclusions:
- FGFR alterations represent a significant driver of human cancer.
- Understanding these alterations is crucial for developing targeted therapies.
- Targeting FGFR signaling holds promise for improving cancer treatment outcomes.
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