Targeting cancer metabolism - aiming at a tumour's sweet-spot

被引:125
|
作者
Jones, Neil P. [1 ]
Schulze, Almut [2 ]
机构
[1] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
[2] Lincolns Inn Fields Labs, Canc Res UK London Res Inst, London WC2A 3LY, England
关键词
INDUCIBLE FACTOR-I; PYRUVATE-KINASE M2; C-MYC; FUMARATE-HYDRATASE; AEROBIC GLYCOLYSIS; LUNG-CANCER; CLINICAL-MANIFESTATIONS; DEHYDROGENASE KINASE; PROLYL HYDROXYLASES; GLUCOSE-METABOLISM;
D O I
10.1016/j.drudis.2011.12.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeting cancer metabolism has emerged as a hot topic for drug discovery. Most cancers have a high demand for metabolic inputs (i.e. glucose/glutamine), which aid proliferation and survival. Interest in targeting cancer metabolism has been renewed in recent years with the discovery that many cancer-related (e.g. oncogenic and tumour suppressor) pathways have a profound effect on metabolism and that many tumours become dependent on specific metabolic processes. Considering the recent increase in our understanding of cancer metabolism and the increasing knowledge of the enzymes and pathways involved, the question arises: could metabolism be cancer's Achilles heel? During recent years, interest into the possible therapeutic benefit of targeting metabolic pathways in cancer has increased dramatically with academic and pharmaceutical groups actively pursuing this aspect of tumour physiology. Therefore, what has fuelled this revived interest in targeting cancer metabolism and what are the major advances and potential challenges faced in the race to develop new therapeutics in this area? This review will attempt to answer these questions by summarising recent developments in this field. We aim to illustrate why we, and others, believe that targeting metabolism in cancer presents such a promising therapeutic rationale.
引用
收藏
页码:232 / 241
页数:10
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