The role of glutamine metabolism in castration-resistant prostate cancer

被引:8
作者
Zhao, Bing [1 ]
Wang, Jing [2 ]
Chen, Li [1 ]
Wang, Hong [3 ]
Liang, Chao-Zhao [4 ,5 ,6 ]
Huang, Jiaoti [7 ,8 ]
Xu, Ling-Fan [4 ,5 ,6 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Geriatr, Div Life Sci & Med, Hefei 230002, Peoples R China
[2] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Urol Oncol, Div Life Sci & Med, Hefei 230031, Peoples R China
[3] Anhui Med Univ, Affiliated Hosp 1, Dept Nursing, Hefei 230001, Peoples R China
[4] Anhui Med Univ, Affiliated Hosp 1, Dept Urol, Hefei 230001, Peoples R China
[5] Anhui Med Univ, Inst Urol, Hefei 230001, Peoples R China
[6] Anhui Med Univ, Anhui Prov Key Lab Genitourinary Dis, Hefei 230001, Peoples R China
[7] Duke Univ, Sch Med, Dept Pathol, Durham, NC 27710 USA
[8] Duke Univ, Duke Canc Inst, Sch Med, Durham, NC 27710 USA
基金
中国国家自然科学基金;
关键词
castration resistance; glutamine metabolism; prostate cancer; tumor metabolism; CELLS; GROWTH; NEUROBLASTOMA; ACTIVATION; INHIBITORS; MOUSE; PTEN;
D O I
10.4103/aja2022105
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
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.
引用
收藏
页码:192 / 197
页数:6
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