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Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.

We have established a subline (EMT6/VRP) of the mouse tumour cell line EMT6/P with acquired resistance to the calcium transport blocker verapamil (VRP). The subline was 4-fold resistant to the cytoxicity of VRP alone compared with the parent line but of similar sensitivity to adriamycin, vincristine...

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Autores principales: Twentyman, P. R., Wright, K. A., Fox, N. E.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971385/
https://www.ncbi.nlm.nih.gov/pubmed/1968761
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author Twentyman, P. R.
Wright, K. A.
Fox, N. E.
author_facet Twentyman, P. R.
Wright, K. A.
Fox, N. E.
author_sort Twentyman, P. R.
collection PubMed
description We have established a subline (EMT6/VRP) of the mouse tumour cell line EMT6/P with acquired resistance to the calcium transport blocker verapamil (VRP). The subline was 4-fold resistant to the cytoxicity of VRP alone compared with the parent line but of similar sensitivity to adriamycin, vincristine or colchicine. EMT6/VRP cells growing in 75 micrograms ml-1 VRP were morphologically different from and larger in diameter than EMT6/P cells, but these two parameters reverted almost to normal within 3 days of VRP removal, although resistance was retained. Expression of an mRNA coding for P-glycoprotein was similar in EMT6/VRP and the parent cell line, although considerable hyperexpression was seen in a multidrug resistant subline, EMT6/AR1.0. Cellular accumulation of both 3H-daunorubicin and 3H-VRP were greater in EMT6/VRP than in the parent line. Sensitisation to adriamycin by 3.3 micrograms ml-1 VRP was, however, somewhat reduced in EMT6/VRP (i.e. to 6.1-fold) compared with the 11-fold sensitisation seen in the parent line. It is clear that resistance to VRP seen in this cell line occurs via a different mechanism from the resistance to drugs such as adriamycin, vincristine and colchicine seen in multidrug resistant cell lines. IMAGES:
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spelling pubmed-19713852009-09-10 Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil. Twentyman, P. R. Wright, K. A. Fox, N. E. Br J Cancer Research Article We have established a subline (EMT6/VRP) of the mouse tumour cell line EMT6/P with acquired resistance to the calcium transport blocker verapamil (VRP). The subline was 4-fold resistant to the cytoxicity of VRP alone compared with the parent line but of similar sensitivity to adriamycin, vincristine or colchicine. EMT6/VRP cells growing in 75 micrograms ml-1 VRP were morphologically different from and larger in diameter than EMT6/P cells, but these two parameters reverted almost to normal within 3 days of VRP removal, although resistance was retained. Expression of an mRNA coding for P-glycoprotein was similar in EMT6/VRP and the parent cell line, although considerable hyperexpression was seen in a multidrug resistant subline, EMT6/AR1.0. Cellular accumulation of both 3H-daunorubicin and 3H-VRP were greater in EMT6/VRP than in the parent line. Sensitisation to adriamycin by 3.3 micrograms ml-1 VRP was, however, somewhat reduced in EMT6/VRP (i.e. to 6.1-fold) compared with the 11-fold sensitisation seen in the parent line. It is clear that resistance to VRP seen in this cell line occurs via a different mechanism from the resistance to drugs such as adriamycin, vincristine and colchicine seen in multidrug resistant cell lines. IMAGES: Nature Publishing Group 1990-02 /pmc/articles/PMC1971385/ /pubmed/1968761 Text en https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Twentyman, P. R.
Wright, K. A.
Fox, N. E.
Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title_full Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title_fullStr Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title_full_unstemmed Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title_short Characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
title_sort characterisation of a mouse tumour cell line with in vitro derived resistance to verapamil.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971385/
https://www.ncbi.nlm.nih.gov/pubmed/1968761
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