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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6207720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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