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Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6

The NIMA (never in mitosis, gene A)-related kinase-6 (NEK6), which is implicated in cell cycle control and plays significant roles in tumorigenesis, is an attractive target for the development of novel anti-cancer drugs. Here we describe the discovery of a potent ATP site-directed inhibitor of NEK6...

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Autores principales: De Donato, Marta, Righino, Benedetta, Filippetti, Flavia, Battaglia, Alessandra, Petrillo, Marco, Pirolli, Davide, Scambia, Giovanni, De Rosa, Maria Cristina, Gallo, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207720/
https://www.ncbi.nlm.nih.gov/pubmed/30375481
http://dx.doi.org/10.1038/s41598-018-34471-y
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author De Donato, Marta
Righino, Benedetta
Filippetti, Flavia
Battaglia, Alessandra
Petrillo, Marco
Pirolli, Davide
Scambia, Giovanni
De Rosa, Maria Cristina
Gallo, Daniela
author_facet De Donato, Marta
Righino, Benedetta
Filippetti, Flavia
Battaglia, Alessandra
Petrillo, Marco
Pirolli, Davide
Scambia, Giovanni
De Rosa, Maria Cristina
Gallo, Daniela
author_sort De Donato, Marta
collection PubMed
description The NIMA (never in mitosis, gene A)-related kinase-6 (NEK6), which is implicated in cell cycle control and plays significant roles in tumorigenesis, is an attractive target for the development of novel anti-cancer drugs. Here we describe the discovery of a potent ATP site-directed inhibitor of NEK6 identified by virtual screening, adopting both structure- and ligand-based techniques. Using a homology-built model of NEK6 as well as the pharmacophoric features of known NEK6 inhibitors we identified novel binding scaffolds. Twenty-five compounds from the top ranking hits were subjected to in vitro kinase assays. The best compound, i.e. compound 8 ((5Z)-2-hydroxy-4-methyl-6-oxo-5-[(5-phenylfuran-2-yl)methylidene]-5,6-dihydropyridine-3-carbonitrile), was able to inhibit NEK6 with low micromolar IC(50) value, also displaying antiproliferative activity against a panel of human cancer cell lines. Our results suggest that the identified inhibitor can be used as lead candidate for the development of novel anti-cancer agents, thus opening the possibility of new therapeutic strategies.
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spelling pubmed-62077202018-11-01 Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6 De Donato, Marta Righino, Benedetta Filippetti, Flavia Battaglia, Alessandra Petrillo, Marco Pirolli, Davide Scambia, Giovanni De Rosa, Maria Cristina Gallo, Daniela Sci Rep Article The NIMA (never in mitosis, gene A)-related kinase-6 (NEK6), which is implicated in cell cycle control and plays significant roles in tumorigenesis, is an attractive target for the development of novel anti-cancer drugs. Here we describe the discovery of a potent ATP site-directed inhibitor of NEK6 identified by virtual screening, adopting both structure- and ligand-based techniques. Using a homology-built model of NEK6 as well as the pharmacophoric features of known NEK6 inhibitors we identified novel binding scaffolds. Twenty-five compounds from the top ranking hits were subjected to in vitro kinase assays. The best compound, i.e. compound 8 ((5Z)-2-hydroxy-4-methyl-6-oxo-5-[(5-phenylfuran-2-yl)methylidene]-5,6-dihydropyridine-3-carbonitrile), was able to inhibit NEK6 with low micromolar IC(50) value, also displaying antiproliferative activity against a panel of human cancer cell lines. Our results suggest that the identified inhibitor can be used as lead candidate for the development of novel anti-cancer agents, thus opening the possibility of new therapeutic strategies. Nature Publishing Group UK 2018-10-30 /pmc/articles/PMC6207720/ /pubmed/30375481 http://dx.doi.org/10.1038/s41598-018-34471-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
De Donato, Marta
Righino, Benedetta
Filippetti, Flavia
Battaglia, Alessandra
Petrillo, Marco
Pirolli, Davide
Scambia, Giovanni
De Rosa, Maria Cristina
Gallo, Daniela
Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title_full Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title_fullStr Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title_full_unstemmed Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title_short Identification and antitumor activity of a novel inhibitor of the NIMA-related kinase NEK6
title_sort identification and antitumor activity of a novel inhibitor of the nima-related kinase nek6
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207720/
https://www.ncbi.nlm.nih.gov/pubmed/30375481
http://dx.doi.org/10.1038/s41598-018-34471-y
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