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Updated: Aug 12, 2026

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An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Keratinocyte growth factor expression in hormone insensitive prostate cancer
1Department of Surgery, The Medical School, University of Newcastle upon Tyne, UK.
Oncogene
|August 28, 1997
Summary
Keratinocyte Growth Factor (KGF) is upregulated in prostate cancer stroma and promotes epithelial cell proliferation. KGF expression correlates with hormone-insensitive tumors, suggesting a role in advanced prostate cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Cellular interactions between prostate stroma and epithelium are crucial for prostate cancer growth.
- Peptide growth factors, such as Keratinocyte Growth Factor (KGF or FGF7), may drive prostate cancer progression.
- KGF has known differentiative and proliferative effects on developing rat prostate epithelium.
Purpose of the Study:
- To investigate KGF as a paracrine agent in human prostate cancer.
- To examine the expression of KGF and its receptors (FGFRs) in prostate cancer.
- To determine the relationship between KGF expression and tumor characteristics.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) for KGF and FGFR mRNA detection.
- In vitro primary culture model to identify KGF source.
- Proliferation assays using recombinant KGF on prostatic epithelial cells.
Main Results:
- KGF mRNA was detected in 65% of prostate cancers (CaP) but not in benign prostatic hyperplasia (BPH).
- KGF expression was upregulated in hormone-insensitive tumors.
- FGFR1IIIb and FGFR2IIIb were expressed in CaP and BPH, while FGFR2IIIc was present in CaP but absent in BPH.
- Recombinant KGF showed a mitogenic effect on prostatic epithelial cells.
Conclusions:
- Prostatic stroma expresses KGF, which acts as a paracrine factor promoting epithelial cell proliferation in prostate cancer.
- KGF upregulation is associated with hormone-insensitive prostate tumors.
- FGFR expression patterns suggest specific roles in prostate cancer, with FGFR2IIIc potentially linked to hormone insensitivity.
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