| Literature DB >> 29909747 |
Ashok Aspatwar1, Holger M Becker2, Nanda Kumar Parvathaneni3,4, Milka Hammaren1, Aleksandra Svorjova1, Harlan Barker1, Claudiu T Supuran5, Ludwig Dubois3, Philippe Lambin3, Mataleena Parikka1, Seppo Parkkila1,6, Jean-Yves Winum4.
Abstract
Carbonic anhydrase (CA) IX is a hypoxia inducible enzyme that is highly expressed in solid tumours. Therefore, it has been considered as an anticancer target using specific chemical inhibitors. The nitroimidazoles DTP338 and DTP348 have been shown to inhibit CA IX in nanomolar range in vitro and reduce extracellular acidification in hypoxia, and impair tumour growth. We screened these compounds for toxicity using zebrafish embryos and measured their in vivo effects on human CA IX in Xenopus oocytes. In the toxicity screening, the LD50 for both compounds was 3.5 mM. Neither compound showed apparent toxicity below 300 µM concentration. Above this concentration, both compounds altered the movement of zebrafish larvae. The IC50 was 0.14 ± 0.02 µM for DTP338 and 19.26 ± 1.97 µM for DTP348, suggesting that these compounds efficiently inhibit CA IX in vivo. Our results suggest that these compounds can be developed as drugs for cancer therapy.Entities:
Keywords: Nitroimidazoles; Xenopus oocytes; carbonic anhydrase IX; in vivo inhibition; zebrafish
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Year: 2018 PMID: 29909747 PMCID: PMC6009478 DOI: 10.1080/14756366.2018.1482285
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051