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Updated: Jul 20, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Novel targets in prostate cancer
Dominik R Berthold1, Malcolm J Moore
1Princess Margaret Hospital and University of Toronto, Department of Medical Oncology and Hematology, 610 University Avenue Toronto, Ontario M5G 2M9, Canada. dominik.berthold@uhn.on.ca
Abstract:
Despite recent advances in the understanding of the cellular and molecular biology of prostate cancer, new options for the treatment of prostate cancer remain elusive. Targeted therapies have shown promising activities in many solid tumours and the growing number of targets and targeted agents is creating numerous opportunities for clinical research in advanced prostate cancer. At ASCO 2006 in Atlanta, a clinical science symposium on novel targets in prostate cancer was presented. It consisted of three abstracts, each of which was followed by a discussant who reviewed the work and placed it in the overall context of current approaches to treating prostate cancer. The three abstracts were a discussion of a new method for quantification of the androgen receptor; the impact of high-dose vitamin D plus chemotherapy on hormone refractory disease and on the risk of thromboembolic disease; and the paradoxical effects seen with the raf-kinase and vascular endothelial growth factor inhibitor sorafenib, which produced improvement in bone scans in the absence of any prostate-specific antigen responses.
Insights
New prostate cancer treatments are emerging. Research presented at ASCO 2006 explored novel targets, vitamin D and chemotherapy combinations, and the effects of targeted therapy sorafenib.
Area of Science:
- Oncology
- Molecular Biology
- Clinical Research
Background:
- Despite advances in prostate cancer biology, novel treatment options remain limited.
- Targeted therapies offer promise for solid tumors, driving clinical research in advanced prostate cancer.
Framework:
- ASCO 2006 symposium focused on novel prostate cancer targets.
- Presentations included androgen receptor quantification, vitamin D/chemotherapy impact, and sorafenib effects.
Implementation:
- A new method for androgen receptor quantification was discussed.
- The impact of high-dose vitamin D plus chemotherapy on hormone-refractory prostate cancer and thromboembolic disease risk was evaluated.
- Paradoxical effects of sorafenib (VEGF/raf-kinase inhibitor) were observed, including bone scan improvements without PSA response.
Implications:
- Findings highlight diverse research avenues for advanced prostate cancer.
- Exploration of novel targets and combination therapies is crucial.
- Understanding paradoxical drug effects like those of sorafenib is key for future treatment strategies.
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