The role of cancer cell bioenergetics in dormancy and drug resistance

被引:8
|
作者
Tau, Steven [1 ]
Miller, Todd W. [1 ,2 ]
机构
[1] Geisel Sch Med Dartmouth, Dartmouth Canc Ctr, Dept Mol & Syst Biol, Lebanon, NH 03756 USA
[2] Dartmouth Hitchcock Med Ctr, One Med Ctr Dr, HB-7936, Lebanon, NH 03756 USA
关键词
Cancer; Tumor; Metabolism; Fatty acid; Energy; Glucose; FATTY-ACID OXIDATION; HUMAN BREAST-CANCER; MYELOID-LEUKEMIA CELLS; CLINICAL-TRIAL; COLON-CANCER; DOUBLE-BLIND; STEM-CELLS; HIGH-RISK; SURVIVAL; GROWTH;
D O I
10.1007/s10555-023-10081-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
While anti-cancer drug treatments are often effective for the clinical management of cancer, these treatments frequently leave behind drug-tolerant persister cancer cells that can ultimately give rise to recurrent disease. Such persistent cancer cells can lie dormant for extended periods of time, going undetected by conventional clinical means. Understanding the mechanisms that such dormant cancer cells use to survive, and the mechanisms that drive emergence from dormancy, is critical to the development of improved therapeutic strategies to prevent and manage disease recurrence. Cancer cells often exhibit metabolic alterations compared to their non-transformed counterparts. An emerging body of evidence supports the notion that dormant cancer cells also have unique metabolic adaptations that may offer therapeutically targetable vulnerabilities. Herein, we review mechanisms through which cancer cells metabolically adapt to persist during drug treatments and develop drug resistance. We also highlight emerging therapeutic strategies to target dormant cancer cells via their metabolic features.
引用
收藏
页码:87 / 98
页数:12
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