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Updated: Nov 10, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Targeting treatment options for castration-resistant prostate cancer
Dannah R Miller1,2, Matthew A Ingersoll1,3, Benjamin A Teply4,5
1Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center Omaha, Nebraska, United States of America.
Prostate cancer (PCa) progresses to castration-resistant PCa (CRPCa) despite androgen-deprivation therapy (ADT). This review explores novel targeting therapies and small molecules to combat lethal CRPCa and improve patient outcomes.
Area of Science:
- Oncology
- Urology
- Pharmacology
Background:
- Prostate cancer (PCa) is a leading cause of cancer death in men.
- Androgen-deprivation therapy (ADT) is standard for metastatic PCa but often leads to castration-resistant PCa (CRPCa).
- Existing treatments for CRPCa extend survival but do not offer a cure.
Purpose of the Study:
- To review recent advances in targeted therapy for prostate cancer.
- To discuss novel small molecules and therapeutic strategies for CRPCa.
- To highlight emerging vulnerabilities in PCa cells beyond androgen signaling.
Main Methods:
- Literature review of recent advancements in prostate cancer targeting therapy.
- Analysis of novel small molecules and their mechanisms of action.
- Discussion of emerging therapeutic strategies including immunotherapies and anti-angiogenesis agents.
Main Results:
- ADT resistance leads to lethal CRPCa.
- Targeting androgen signaling and docetaxel remain key, but new approaches are needed.
- Novel small molecules, immunotherapies, and anti-angiogenesis agents show promise.
Conclusions:
- Targeted therapies offer new hope for treating advanced prostate cancer.
- Exploiting PCa cell vulnerabilities is crucial for overcoming treatment resistance.
- Further research into novel small molecules and combination therapies is warranted for CRPCa.
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