| Literature DB >> 26879218 |
Yizhen Yin1, Shigeki Sasaki1, Yosuke Taniguchi2.
Abstract
hMTH1 (8-oxo-2'-deoxyguanine triphosphatase) hydrolyzes oxidized nucleoside triphosphates; its presence is non-essential for survival of normal cells but is required for survival of cancer cells. In this study, 8-halogenated-7-deaza-2'-deoxyguanosine triphosphate (8-halogenated-7-deazadGTP) derivatives were synthesized. Interestingly, these triphosphates were poor substrates for hMTH1, but exhibited strong competitive inhibition against hMTH1 at nanomolar levels. This inhibitory effect is attributed to slower rate of hydrolysis, possibly arising from enzyme structural changes, specifically different stacking interactions with 8-halogenated-7-deazadGTP. This is the first example of using nucleotide derivatives to inhibit hMTH1, thus demonstrating their potential as antitumor agents.Entities:
Keywords: cancer; hMTH1; halogenated deazadeoxyguanosine triphosphate; inhibitors; oxo-dGTP
Mesh:
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Year: 2016 PMID: 26879218 DOI: 10.1002/cbic.201500589
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164