Reprogramming of central carbon metabolism in cancer stem cells

被引:65
作者
Wong, Tin Lok [1 ]
Che, Noelia [1 ]
Ma, Stephanie [1 ,2 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Sch Biomed Sci, 1-F,Lab Block,21 Sassoon Rd, Pok Fu Lam, Hong Kong, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, State Key Lab Liver Res, Hong Kong, Hong Kong, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2017年 / 1863卷 / 07期
关键词
Cancer stem cells; Metabolism; Glycolysis; OXPHOS; Metabolic rewiring; Tumor-initiating cells; TUMOR-INITIATING CELLS; OXIDATIVE-PHOSPHORYLATION; BREAST-CANCER; GLUCOSE-METABOLISM; PANCREATIC-CANCER; SELF-RENEWAL; HEPATOCELLULAR-CARCINOMA; GLYCOLYTIC METABOLISM; GLUTAMINE-METABOLISM; THERAPEUTIC TARGET;
D O I
10.1016/j.bbadis.2017.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer metabolism has been studied for years and adopted in the clinic for monitoring disease progression and therapy response. Despite our growing knowledge of a distinctly altered metabolic behavior in cancer, drugs targeting cancer metabolism have remained less than promising. Recent efforts in cancer stem cell (CSC) biology suggest that a subpopulation of tumor-initiating cells within the tumor bulk represents the root of tumor recurrence and therapy resistance. In recent years, metabolic phenotype of CSCs of various tumor types has been identified. This breakthrough has shed light on the underlying mechanism by which CSCs maintain stemness, confer resistance to therapies and initiate tumor relapse. The distinct metabolic characteristics of CSCs compared to non-CSCs provide an opportunity to target CSCs more specifically and have become a major focus in cancer research in recent years with substantial efforts conducted towards discovering clinical targets. This perspective article summarizes the current knowledge of CSC metabolism in carcinogenesis and highlights the potential of targeting CSC metabolism for therapy.
引用
收藏
页码:1728 / 1738
页数:11
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