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An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
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MET expression during prostate cancer progression.
Esther I Verhoef1, Kimberley Kolijn1, Maria J De Herdt2
1Department of Pathology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Oncotarget
|April 23, 2016
Summary
Hepatocyte growth factor receptor MET is expressed in advanced prostate cancer, particularly bone metastases. MET evaluation may help stratify patients for targeted therapies in hormone-refractory prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Hepatocyte growth factor receptor MET inhibitors are explored for hormone-refractory prostate cancer (HRPC) metastasis treatment.
- Analyzing MET expression and genetic alterations can aid in stratifying prostate cancer patients for therapy.
Purpose of the Study:
- To investigate MET expression and alterations at protein, DNA, and RNA levels across various stages of prostate cancer progression.
Main Methods:
- Immunohistochemistry for MET protein expression.
- In situ hybridization for MET mRNA levels and DNA copy numbers.
- Analysis in hormone-naive primary prostate cancers, lymph node metastases, HRPC, and bone metastases.
Main Results:
- MET expression was absent in hormone-naive primary prostate cancer and lymph node metastases.
- MET protein and mRNA were detected in 23% and 26% of HRPC resections, respectively, without MET amplification.
- MET protein expression was high in bone metastases (88% hormone-naive, 67% HRPC), with MET polysomy in 61% of evaluable cases.
Conclusions:
- MET is predominantly expressed in HRPC and prostate cancer bone metastases.
- MET expression in late-stage prostate cancer is not linked to MET amplification or polysomy.
- Assessing MET status is crucial for therapeutic stratification in advanced prostate cancer.
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