Stalling the Engine of Resistance: Targeting Cancer Metabolism to Overcome Therapeutic Resistance

被引:104
作者
Butler, Ethan B. [1 ]
Zhao, Yuhua [1 ,3 ]
Munoz-Pinedo, Cristina [4 ]
Lu, Jianrong [5 ]
Tan, Ming [1 ,2 ]
机构
[1] Univ S Alabama, Mitchell Canc Inst, Mobile, AL 36604 USA
[2] Univ S Alabama, Dept Cell Biol & Neurosci, Mobile, AL 36604 USA
[3] Sichuan Univ, West China Sch Preclin & Forens Med, Chengdu, Peoples R China
[4] Bellvitge Biomed Res Inst IDI BELL, Barcelona, Spain
[5] Univ Florida, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
关键词
STRUCTURAL DERIVATIVE TT-232; HEAT-SHOCK FACTOR-1; DRUG-RESISTANCE; BREAST-CANCER; IN-VITRO; ANTITUMOR-ACTIVITY; LACTATE-DEHYDROGENASE; PANCREATIC-CANCER; CELL GROWTH; GLUTAMINE-METABOLISM;
D O I
10.1158/0008-5472.CAN-12-3009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer cells are markedly different from normal cells with regards to how their metabolic pathways are used to fuel cellular growth and survival. Two basic metabolites that exemplify these differences through increased uptake and altered metabolic usage are glucose and glutamine. These molecules can be catabolized to manufacture many of the building blocks required for active cell growth and proliferation. The alterations in the metabolic pathways necessary to sustain this growth have been linked to therapeutic resistance, a trait that is correlated with poor patient outcomes. By targeting the metabolic pathways that import, catabolize, and synthesize essential cellular components, drug-resistant cancer cells can often be resensitized to anticancer treatments. The specificity and efficacy of agents directed at the unique aspects of cancer metabolism are expected to be high; and may, when in used in combination with more traditional therapeutics, present a pathway to surmount resistance within tumors that no longer respond to current forms of treatment. (C) 2013 AACR.
引用
收藏
页码:2709 / 2717
页数:9
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