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Updated: Aug 14, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
The role of glutamine metabolism in castration-resistant prostate cancer
Bing Zhao1, Jing Wang2, Li Chen1
1Department of Geriatrics, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230002, China.
Abstract:
Reprogramming of metabolism is a hallmark of tumors, which has been explored for therapeutic purposes. Prostate cancer (PCa), particularly advanced and therapy-resistant PCa, displays unique metabolic properties. Targeting metabolic vulnerabilities in PCa may benefit patients who have exhausted currently available treatment options and improve clinical outcomes. Among the many nutrients, glutamine has been shown to play a central role in the metabolic reprogramming of advanced PCa. In addition to amino acid metabolism, glutamine is also widely involved in the synthesis of other macromolecules and biomasses. Targeting glutamine metabolic network by maximally inhibiting glutamine utilization in tumor cells may significantly add to treatment options for many patients. This review summarizes the metabolic landscape of PCa, with a particular focus on recent studies of how glutamine metabolism alterations affect therapeutic resistance and disease progression of PCa, and suggests novel therapeutic strategies.
Insights
Targeting glutamine metabolism in advanced prostate cancer (PCa) offers a promising therapeutic strategy. Inhibiting glutamine utilization in tumor cells could improve treatment options for patients with therapy-resistant PCa.
Area of Science:
- Oncology
- Metabolic pathways
- Cancer biology
Background:
- Tumor cells exhibit metabolic reprogramming, a key area for therapeutic exploration.
- Advanced and therapy-resistant prostate cancer (PCa) presents unique metabolic characteristics.
- Glutamine plays a critical role in the metabolic reprogramming of advanced PCa.
Purpose of the Study:
- To review the metabolic landscape of prostate cancer.
- To focus on how altered glutamine metabolism impacts therapeutic resistance and disease progression in PCa.
- To suggest novel therapeutic strategies targeting glutamine metabolism.
Main Methods:
- Literature review of recent studies on prostate cancer metabolism.
- Analysis of glutamine's role in PCa metabolic reprogramming.
- Identification of therapeutic vulnerabilities related to glutamine utilization.
Main Results:
- Glutamine is central to metabolic reprogramming in advanced PCa.
- Altered glutamine metabolism is linked to therapeutic resistance and disease progression.
- Inhibiting glutamine utilization presents a potential therapeutic avenue.
Conclusions:
- Targeting the glutamine metabolic network is a viable strategy for PCa treatment.
- Maximally inhibiting glutamine utilization may benefit patients with limited options.
- Further research into glutamine metabolism could lead to improved clinical outcomes for PCa patients.
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