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PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study
ABCB1 overexpression significantly desensitized both drug-selected and gene-transfected cells, which overexpress ABCB1, to OTS964 and that this drug resistance can be antagonized by verapamil, a known ABCB1 inhibitor. Consistently, a similar trend was observed in tumor-bearing mice. OTS964 stimulate...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822834/ https://www.ncbi.nlm.nih.gov/pubmed/35135547 http://dx.doi.org/10.1186/s12943-022-01512-0 |
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author | Yang, Yuqi Teng, Qiu-Xu Wu, Zhuo-Xun Wang, Jing-Quan Lei, Zi-Ning Lusvarghi, Sabrina Ambudkar, Suresh V. Ji, Ning Chen, Zhe-Sheng |
author_facet | Yang, Yuqi Teng, Qiu-Xu Wu, Zhuo-Xun Wang, Jing-Quan Lei, Zi-Ning Lusvarghi, Sabrina Ambudkar, Suresh V. Ji, Ning Chen, Zhe-Sheng |
author_sort | Yang, Yuqi |
collection | PubMed |
description | ABCB1 overexpression significantly desensitized both drug-selected and gene-transfected cells, which overexpress ABCB1, to OTS964 and that this drug resistance can be antagonized by verapamil, a known ABCB1 inhibitor. Consistently, a similar trend was observed in tumor-bearing mice. OTS964 stimulated ATPase activity of ABCB1 and upregulated expression levels of ABCB1, resulting in induced resistance to other ABCB1 substrate-drugs, such as paclitaxel. OTS964 received a comparable affinity score and can dock into the substrate-binding site of human ABCB1 protein. . SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-022-01512-0. |
format | Online Article Text |
id | pubmed-8822834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88228342022-02-08 PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study Yang, Yuqi Teng, Qiu-Xu Wu, Zhuo-Xun Wang, Jing-Quan Lei, Zi-Ning Lusvarghi, Sabrina Ambudkar, Suresh V. Ji, Ning Chen, Zhe-Sheng Mol Cancer Letter to the Editor ABCB1 overexpression significantly desensitized both drug-selected and gene-transfected cells, which overexpress ABCB1, to OTS964 and that this drug resistance can be antagonized by verapamil, a known ABCB1 inhibitor. Consistently, a similar trend was observed in tumor-bearing mice. OTS964 stimulated ATPase activity of ABCB1 and upregulated expression levels of ABCB1, resulting in induced resistance to other ABCB1 substrate-drugs, such as paclitaxel. OTS964 received a comparable affinity score and can dock into the substrate-binding site of human ABCB1 protein. . SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-022-01512-0. BioMed Central 2022-02-08 /pmc/articles/PMC8822834/ /pubmed/35135547 http://dx.doi.org/10.1186/s12943-022-01512-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter to the Editor Yang, Yuqi Teng, Qiu-Xu Wu, Zhuo-Xun Wang, Jing-Quan Lei, Zi-Ning Lusvarghi, Sabrina Ambudkar, Suresh V. Ji, Ning Chen, Zhe-Sheng PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title | PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title_full | PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title_fullStr | PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title_full_unstemmed | PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title_short | PBK/TOPK inhibitor OTS964 resistance is mediated by ABCB1-dependent transport function in cancer: in vitro and in vivo study |
title_sort | pbk/topk inhibitor ots964 resistance is mediated by abcb1-dependent transport function in cancer: in vitro and in vivo study |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822834/ https://www.ncbi.nlm.nih.gov/pubmed/35135547 http://dx.doi.org/10.1186/s12943-022-01512-0 |
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