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Updated: Apr 30, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Recent advances in bone-targeted therapies of metastatic prostate cancer
Xiyun Deng1, Guangchun He2, Junwen Liu3
1College of Medicine, Hunan Normal University, Changsha, Hunan 410013, China; Changsha Microworld Biotech Company, Changsha, Hunan 410004, China.
Abstract:
Prostate cancer is one of the most common malignancies affecting men worldwide, with bone being the most common site of metastasis in patients that progress beyond organ confinement. Bone metastases are virtually incurable and result in significant disease morbidity and mortality. Bone provides a unique microenvironment whose local interactions with tumor cells offer novel targets for therapeutic interventions. Several attractive molecules or pathways have been identified as new potential therapeutic targets for bone metastases caused by metastatic castration-resistant prostate cancer. In this review, we present the recent advances in molecular targeted therapies for prostate cancer bone metastasis focusing on therapies that target the bone cells and the bone microenvironment. The therapies covered in this review include agents that inhibit bone resorption, agents that stimulate bone formation, and agents that target the bone matrix. Suggestions to devise more effective molecular targeted therapies are proposed. Hopefully, with better understanding of the biology of the disease and the development of more robust targeted therapies, the survival and quality of life of the affected individuals could be significantly improved.
Insights
This review explores novel molecular targeted therapies for prostate cancer bone metastasis, focusing on treatments that interact with the bone microenvironment. Advances aim to improve survival and quality of life for patients with bone metastases.
Area of Science:
- Oncology
- Bone Metastasis Research
- Molecular Therapeutics
Background:
- Prostate cancer frequently metastasizes to bone, leading to incurable conditions with high morbidity and mortality.
- The bone microenvironment presents unique interactions with tumor cells, offering potential therapeutic targets.
- Metastatic castration-resistant prostate cancer (mCRPC) bone metastases are a significant clinical challenge.
Purpose of the Study:
- To review recent advances in molecular targeted therapies for prostate cancer bone metastasis.
- To focus on therapies targeting bone cells and the bone microenvironment.
- To propose strategies for developing more effective targeted therapies.
Main Methods:
- Literature review of recent advances in molecular targeted therapies for prostate cancer bone metastasis.
- Categorization of therapies based on their mechanism of action (inhibition of bone resorption, stimulation of bone formation, targeting bone matrix).
- Analysis of therapeutic strategies targeting the bone microenvironment.
Main Results:
- Identification of several promising molecular targets and pathways for treating bone metastases.
- Overview of therapeutic agents that modulate bone resorption, formation, and matrix.
- Discussion of the potential of targeting the bone microenvironment for novel treatments.
Conclusions:
- Targeted therapies focusing on the bone microenvironment hold significant promise for treating prostate cancer bone metastasis.
- Further understanding of disease biology and development of robust therapies can improve patient survival and quality of life.
- Novel therapeutic strategies are emerging to combat the challenges of bone metastases in prostate cancer.
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