Targeting the Warburg Effect in cancer; relationships for 2-arylpyridazinones as inhibitors of the key glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3)

被引:34
作者
Brooke, Darby G. [1 ]
van Dam, Ellen M. [2 ]
Watts, Colin K. W. [2 ]
Khoury, Amanda [2 ]
Dziadek, Marie A. [2 ]
Brooks, Hilary [2 ]
Graham, Lisa-Jane K. [2 ]
Flanagan, Jack U. [1 ,3 ]
Denny, William A. [1 ,3 ]
机构
[1] Univ Auckland, Sch Med Sci, Auckland Canc Soc Res Ctr, Auckland 1142, New Zealand
[2] Garvan Inst Med Res, Sydney, NSW 2010, Australia
[3] Univ Auckland, Maurice Wilkins Ctr Mol Biodiscovery, Auckland 1142, New Zealand
关键词
Glycolysis; PFKFB3; Pyridazinone; Warburg Effect; 6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE PFKFB3; GENE; VALIDATION; METABOLISM;
D O I
10.1016/j.bmc.2013.12.041
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
High-throughput screening of a small-molecule library identified a 5-triazolo-2-arylpyridazinone as a novel inhibitor of the important glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3). Such inhibitors are of interest due to PFKFB3's control of the important glycolytic pathway used by cancer cells to generate ATP. A series of analogues was synthesized to study structure-activity relationships key to enzyme inhibition. Changes to the triazolo or pyridazinone rings were not favoured, but limited-size substitutions on the aryl ring provided modest increases in potency against the enzyme. Selected analogues and literature-described inhibitors were evaluated for their ability to suppress the glycolytic pathway, as detected by a decrease in lactate production, but none of these compounds demonstrated such suppression at non-cytotoxic concentrations. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1029 / 1039
页数:11
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