Tumor metabolism of lactate: the influence and therapeutic potential for MCT and CD147 regulation

被引:109
作者
Kennedy, Kelly M. [1 ]
Dewhirst, Mark W. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
关键词
cancer; CD147; lactate; MCT1; inhibitors; MCT4; tumor metabolism; MATRIX-METALLOPROTEINASE INDUCER; GAMMA-HYDROXYBUTYRIC ACID; SQUAMOUS-CELL CARCINOMA; CHAIN FATTY-ACIDS; COLONIC MONOCARBOXYLATE TRANSPORTER; REGIONAL QUANTITATIVE-DETERMINATION; INTRACELLULAR PH INDICATOR; CARBONIC-ANHYDRASE II; BREAST-CANCER CELLS; C6; GLIOMA-CELLS;
D O I
10.2217/FON.09.145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor metabolism consists of complex interactions between oxygenation states, metabolites, ions, the vascular network and signaling cascades, Accumulation of lactate within tumors has been correlated with poor clinical outcomes. While its production has negative implications, potentially contributing to tumor progression, the implications of the ability of tumors to utilize lactate can offer new therapeutic targets for the future. Monocarboxylate transporters (MCTs) of the SLC16A gene family influence substrate availability, the metabolic path of lactate and pH balance within the tumor. CD147, a chaperone to some MCT subtypes, contributes to tumor progression and metastasis. The implications and consequences of lactate utilization by tumors are currently unknown; therefore future research is needed on the intricacies of tumor metabolism. The possibility of metabolic modification of the tumor microenvironment via regulation or manipulation of MCTI and CD147 may prove to be promising avenues of therapeutic options.
引用
收藏
页码:127 / 148
页数:22
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