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Updated: Feb 9, 2026

An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Drug Repositioning for Effective Prostate Cancer Treatment
Beste Turanli1,2,3, Morten Grøtli4, Jan Boren5
1Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden.
Abstract:
Drug repositioning has gained attention from both academia and pharmaceutical companies as an auxiliary process to conventional drug discovery. Chemotherapeutic agents have notorious adverse effects that drastically reduce the life quality of cancer patients so drug repositioning is a promising strategy to identify non-cancer drugs which have anti-cancer activity as well as tolerable adverse effects for human health. There are various strategies for discovery and validation of repurposed drugs. In this review, 25 repurposed drug candidates are presented as result of different strategies, 15 of which are already under clinical investigation for treatment of prostate cancer (PCa). To date, zoledronic acid is the only repurposed, clinically used, and approved non-cancer drug for PCa. Anti-cancer activities of existing drugs presented in this review cover diverse and also known mechanisms such as inhibition of mTOR and VEGFR2 signaling, inhibition of PI3K/Akt signaling, COX and selective COX-2 inhibition, NF-κB inhibition, Wnt/β-Catenin pathway inhibition, DNMT1 inhibition, and GSK-3β inhibition. In addition to monotherapy option, combination therapy with current anti-cancer drugs may also increase drug efficacy and reduce adverse effects. Thus, drug repositioning may become a key approach for drug discovery in terms of time- and cost-efficiency comparing to conventional drug discovery and development process.
Insights
Drug repositioning identifies existing non-cancer drugs with anti-cancer properties, offering safer alternatives for cancer treatment. This review highlights 25 candidates, including 15 for prostate cancer (PCa), showcasing a cost-effective discovery approach.
Area of Science:
- Oncology
- Pharmacology
- Drug Discovery
Background:
- Conventional chemotherapy causes severe adverse effects, reducing cancer patient quality of life.
- Drug repositioning offers a promising strategy to find non-cancer drugs with anti-cancer activity and better safety profiles.
- Identifying repurposed drugs can complement traditional drug discovery, potentially reducing time and cost.
Purpose of the Study:
- To review drug repositioning strategies for identifying anti-cancer agents.
- To present repurposed drug candidates, particularly for prostate cancer (PCa) treatment.
- To summarize the anti-cancer mechanisms and therapeutic potential of repurposed drugs.
Main Methods:
- Literature review of drug repositioning strategies and identified candidates.
- Compilation of 25 repurposed drug candidates based on various discovery approaches.
- Analysis of clinical investigation status and approved repurposed drugs for PCa.
Main Results:
- Fifteen repurposed drug candidates are under clinical investigation for prostate cancer (PCa).
- Zoledronic acid is the sole repurposed, approved non-cancer drug for PCa.
- Identified drugs target diverse mechanisms including mTOR, VEGFR2, PI3K/Akt, COX, NF-κB, Wnt/β-Catenin, DNMT1, and GSK-3β pathways.
Conclusions:
- Drug repositioning is an efficient strategy for discovering novel anti-cancer therapeutics.
- Repurposed drugs offer potential for both monotherapy and combination therapy to improve efficacy and reduce toxicity.
- This approach represents a significant advancement in time- and cost-efficient drug discovery for cancer treatment.
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