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ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib
BACKGROUND: Recently, we have shown that the ATP-binding cassette (ABC) transporter ABCB1 interferes with the anti-cancer activity of the pan-aurora kinase inhibitor tozasertib (VX680, MK-0457) but not of the aurora kinase A and B inhibitor alisertib (MLN8237). Preliminary data had suggested tozaser...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587578/ https://www.ncbi.nlm.nih.gov/pubmed/26415506 http://dx.doi.org/10.1186/s13104-015-1405-4 |
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author | Michaelis, Martin Selt, Florian Rothweiler, Florian Wiese, Michael Cinatl, Jindrich |
author_facet | Michaelis, Martin Selt, Florian Rothweiler, Florian Wiese, Michael Cinatl, Jindrich |
author_sort | Michaelis, Martin |
collection | PubMed |
description | BACKGROUND: Recently, we have shown that the ATP-binding cassette (ABC) transporter ABCB1 interferes with the anti-cancer activity of the pan-aurora kinase inhibitor tozasertib (VX680, MK-0457) but not of the aurora kinase A and B inhibitor alisertib (MLN8237). Preliminary data had suggested tozasertib also to be a substrate of the ABC transporter ABCG2, another ABC transporter potentially involved in cancer cell drug resistance. Here, we studied the effect of ABCG2 on the activity of tozasertib and alisertib. RESULTS: The tozasertib concentration that reduces cell viability by 50 % (IC(50)) was dramatically increased in ABCG2-transduced UKF-NB-3(ABCG2) cells (48.8-fold) compared to UKF-NB-3 cells and vector-transduced control cells. The ABCG2 inhibitor WK-X-34 reduced tozasertib IC(50) to the level of non-ABCG2-expressing UKF-NB-3 cells. Furthermore, ABCG2 depletion from UKF-NB-3(ABCG2) cells using another lentiviral vector expressing an shRNA against the bicistronic mRNA of ABCG2 and eGFP largely re-sensitised these cells to tozasertib. In contrast, alisertib activity was not affected by ABCG2 expression. CONCLUSIONS: Tozasertib but not alisertib activity is affected by ABCG2 expression. This should be considered within the design and analysis of experiments and clinical trials investigating these compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1405-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4587578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45875782015-09-30 ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib Michaelis, Martin Selt, Florian Rothweiler, Florian Wiese, Michael Cinatl, Jindrich BMC Res Notes Short Report BACKGROUND: Recently, we have shown that the ATP-binding cassette (ABC) transporter ABCB1 interferes with the anti-cancer activity of the pan-aurora kinase inhibitor tozasertib (VX680, MK-0457) but not of the aurora kinase A and B inhibitor alisertib (MLN8237). Preliminary data had suggested tozasertib also to be a substrate of the ABC transporter ABCG2, another ABC transporter potentially involved in cancer cell drug resistance. Here, we studied the effect of ABCG2 on the activity of tozasertib and alisertib. RESULTS: The tozasertib concentration that reduces cell viability by 50 % (IC(50)) was dramatically increased in ABCG2-transduced UKF-NB-3(ABCG2) cells (48.8-fold) compared to UKF-NB-3 cells and vector-transduced control cells. The ABCG2 inhibitor WK-X-34 reduced tozasertib IC(50) to the level of non-ABCG2-expressing UKF-NB-3 cells. Furthermore, ABCG2 depletion from UKF-NB-3(ABCG2) cells using another lentiviral vector expressing an shRNA against the bicistronic mRNA of ABCG2 and eGFP largely re-sensitised these cells to tozasertib. In contrast, alisertib activity was not affected by ABCG2 expression. CONCLUSIONS: Tozasertib but not alisertib activity is affected by ABCG2 expression. This should be considered within the design and analysis of experiments and clinical trials investigating these compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1405-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-28 /pmc/articles/PMC4587578/ /pubmed/26415506 http://dx.doi.org/10.1186/s13104-015-1405-4 Text en © Michaelis et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Michaelis, Martin Selt, Florian Rothweiler, Florian Wiese, Michael Cinatl, Jindrich ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title | ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title_full | ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title_fullStr | ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title_full_unstemmed | ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title_short | ABCG2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
title_sort | abcg2 impairs the activity of the aurora kinase inhibitor tozasertib but not of alisertib |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587578/ https://www.ncbi.nlm.nih.gov/pubmed/26415506 http://dx.doi.org/10.1186/s13104-015-1405-4 |
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