Small-Molecule Inhibitors of Tankyrases as Prospective Therapeutics for Cancer

被引:24
作者
Yu, Mingfeng [1 ]
Yang, Yuchao [1 ]
Sykes, Matthew [1 ]
Wang, Shudong [1 ]
机构
[1] Univ South Australia, Clin & Hlth Sci, Drug Discovery & Dev, Adelaide, SA 5000, Australia
关键词
WNT/BETA-CATENIN PATHWAY; MESSENGER-RNA EXPRESSION; CANONICAL WNT PATHWAY; POLY-ADP RIBOSYLATION; STERILE ALPHA MOTIF; POLY(ADP-RIBOSE) POLYMERASE; BETA-CATENIN; STRUCTURAL BASIS; COLON-CANCER; SUBSTRATE RECOGNITION;
D O I
10.1021/acs.jmedchem.1c02139
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tankyrases are multifunctional poly(adenosine diphosphate-ribose) polymerases that regulate diverse biologicalprocesses including telomere maintenance and cellular signaling. These processes are often implicated in a number of humandiseases, with cancer being the most prevalent example. Accordingly, tankyrase inhibitors have gained increasing attention aspotential therapeutics. Since the discovery of XAV939 and IWR-1 as thefirst tankyrase inhibitors over two decades ago, tankyrase-targeted drug discovery has made significant progress. This review starts with an introduction of tankyrases, with emphasis placed ontheir cancer-related functions. Small-molecule inhibitors of tankyrases are subsequently delineated based on their distinct modes ofbinding to the enzymes. In addition to inhibitors that compete with oxidized nicotinamide adenine dinucleotide (NAD+) for bindingto the catalytic domain of tankyrases, non-NAD+-competitive inhibitors are detailed. This is followed by a description of threeclinically trialled tankyrase inhibitors. To conclude, some of challenges and prospects in developing tankyrase-targeted cancertherapies are discussed.
引用
收藏
页码:5244 / 5273
页数:30
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