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Updated: Apr 21, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Metastasis as a therapeutic target in prostate cancer: a conceptual framework
Konstantin Stoletov1, David Bond1, Katie Hebron2
1Department of Oncology, University of Alberta, 5-142C Katz Group Building, 114th St and 87th Ave, Edmonton, AB T6G 2E1 Canada.
Abstract:
Metastasis is the main cause of prostate cancer-associated deaths. While significant progerss has been made in the treatment of primary tumors, efficent therapies that target the metastatic spread of prostate cancer are far from clinical reality. To efficiently treat cancer we need be able to impede its spread. Unfortunately, the majority of current therapeutics approved to treat metastatic cancer were originally selected based on their ability to inhibit primary tumor growth. This inherent flaw precluded these therapies from efficiently targeting the development of secondary metastatic lesions, a process that is distinct from that of primary tumor progression. In this review we will summarize the conceptual, cellular and molecular targets that should be considered to design effective anti-metastatic therapies.
Insights
Metastasis drives prostate cancer deaths, yet current treatments targeting primary tumors fail to stop cancer spread. This review explores new targets for effective anti-metastatic therapies.
Area of Science:
- Oncology
- Cancer Metastasis Research
Background:
- Prostate cancer metastasis is the primary cause of cancer-related mortality.
- Current therapies primarily target primary tumors, not metastatic spread.
- Existing treatments for metastatic cancer were developed for primary tumor inhibition, overlooking distinct metastatic processes.
Purpose of the Study:
- To review conceptual, cellular, and molecular targets for effective anti-metastatic therapies.
- To highlight the need for therapies specifically designed to impede cancer spread.
- To address the limitations of current treatments in targeting secondary metastatic lesions.
Main Methods:
- Literature review of existing research on prostate cancer metastasis.
- Analysis of conceptual, cellular, and molecular targets for anti-metastatic drug development.
- Synthesis of information to guide the design of novel therapeutic strategies.
Main Results:
- Identified a critical gap in current prostate cancer treatment regarding metastatic spread.
- Highlighted that primary tumor growth inhibition does not equate to metastatic lesion control.
- Established the distinct biological processes involved in primary tumor progression versus metastatic development.
Conclusions:
- Effective anti-metastatic therapies require targeting distinct cellular and molecular pathways.
- A paradigm shift is needed from primary tumor-centric treatments to metastasis-focused strategies.
- Future research should prioritize the identification and validation of novel anti-metastatic targets.
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