A paradigm for the treatment of prostate cancer bone metastases based on an understanding of tumor cell-microenvironment interactions
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Updated: Aug 17, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Robert D Loberg1, Bishoy A Gayed, Karin B Olson
1Department of Urology, University of Michigan Urology Center, The University of Michigan, Ann Arbor, Michigan 48109-0946, USA. rloberg@umich.edu
Abstract:
The pliability of cancer cells to mutate into several different phenotypes in an attempt to find one that will survive and colonize at the metastatic site is a tremendous "hurdle" to overcome in designing novel cancer therapeutics. New targets of therapy are essential if we are to effectively overcome the evasiveness of cancer. The interaction between the tumor cell and the surrounding microenvironment creates a vicious cycle that perpetuates disease survival and progression. The future of cancer therapy resides in the ability to focus on the recruited and exploited relationships of the cancer cell with the host environment. These therapies target cancer cell growth early and interrupt the vicious cycle that is created by the tumor cells interacting with bone components by inhibiting osteoclasts, osteoblasts, stromal cells, and endothelial cells. They alter the bone microenvironment, creating a hostile "soil" that prevents the "seed" from developing into bone metastases and represent a potential new platform for the development of prostate cancer therapeutics.
Insights
Cancer cells
Area of Science:
- Oncology
- Cancer Metastasis
- Tumor Microenvironment
Background:
- Cancer cells' ability to mutate into diverse phenotypes presents a significant challenge for developing effective cancer therapeutics.
- The tumor microenvironment's interaction with cancer cells drives disease progression and survival.
- Novel therapeutic targets are crucial to overcome cancer's evasiveness.
Purpose of the Study:
- To explore new therapeutic strategies targeting the interplay between cancer cells and their microenvironment.
- To identify methods to interrupt the cycle of disease progression perpetuated by tumor-host interactions.
- To investigate therapies that modify the bone microenvironment to prevent bone metastasis.
Main Methods:
- Focusing on therapies that target the relationships between cancer cells and the host environment.
- Inhibiting key cellular components within the bone microenvironment, including osteoclasts, osteoblasts, stromal cells, and endothelial cells.
- Developing strategies to alter the bone microenvironment to create a hostile environment for metastatic cancer cells.
Main Results:
- Therapies targeting tumor-host interactions can inhibit cancer cell growth.
- Interrupting the vicious cycle created by tumor cells and bone components is achievable.
- Modifying the bone microenvironment can prevent the development of bone metastases.
Conclusions:
- Targeting the tumor microenvironment and its interactions with cancer cells offers a promising therapeutic avenue.
- Altering the bone microenvironment can create hostile conditions for cancer cell colonization, preventing bone metastases.
- This approach represents a potential new platform for developing novel prostate cancer therapeutics.
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