The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer

The antiestrogen tamoxifen was examined for its effect on the interaction of monoclonal antibodies with the multidrug resistance markers: with Pgp and MRP1 in the cultured T-lymphoblast leukemia cell line Jurkat and with BCRP in the cultured cervical cancer cell line HeLa. The investigation used imm...

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Main Authors: T. A. Bogush, E. A. Dudko, E. A. Bogush, B. E. Polotsky, S. A. Tyulyandin, M. I. Davydov
Format: Article
Language:Russian
Published: ABV-press 2014-07-01
Series:Опухоли женской репродуктивной системы
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Online Access:https://ojrs.abvpress.ru/ojrs/article/view/136
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author T. A. Bogush
E. A. Dudko
E. A. Bogush
B. E. Polotsky
S. A. Tyulyandin
M. I. Davydov
author_facet T. A. Bogush
E. A. Dudko
E. A. Bogush
B. E. Polotsky
S. A. Tyulyandin
M. I. Davydov
author_sort T. A. Bogush
collection DOAJ
description The antiestrogen tamoxifen was examined for its effect on the interaction of monoclonal antibodies with the multidrug resistance markers: with Pgp and MRP1 in the cultured T-lymphoblast leukemia cell line Jurkat and with BCRP in the cultured cervical cancer cell line HeLa. The investigation used immunofluorescence and flow cytofluorimetric assays, primary monoclonal and isotypic antibodies labeled with the fluorescent dyes FITS and PE. After tamoxifen use, there was an increase in specific fluorescence and the number of specifically fluorescent cells on incubation with Pgp and BCRP antibodies and a reduction in those on incubation with MRP1 antibodies. This directly indicates that tomoxifen binds to Pgp, BCRP, and MRP1, which inevitably results in a decrease in the intracellular concentration of the antiestrogen available for the interaction with other cellular targets, including that with estrogen receptors. The authors consider that there is every reason to consider Pgp, BCRP, and MRP1 as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer with the positive estrogen receptor status.
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institution Kabale University
issn 1994-4098
1999-8627
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series Опухоли женской репродуктивной системы
spelling doaj-art-fab5e624342a49eba5cd663e2402dbc42025-08-20T03:37:11ZrusABV-pressОпухоли женской репродуктивной системы1994-40981999-86272014-07-010181810.17650/1994-4098-2011-0-1-8-18152The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancerT. A. Bogush0E. A. Dudko1E. A. Bogush2B. E. Polotsky3S. A. Tyulyandin4M. I. Davydov5N.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, MoscowThe antiestrogen tamoxifen was examined for its effect on the interaction of monoclonal antibodies with the multidrug resistance markers: with Pgp and MRP1 in the cultured T-lymphoblast leukemia cell line Jurkat and with BCRP in the cultured cervical cancer cell line HeLa. The investigation used immunofluorescence and flow cytofluorimetric assays, primary monoclonal and isotypic antibodies labeled with the fluorescent dyes FITS and PE. After tamoxifen use, there was an increase in specific fluorescence and the number of specifically fluorescent cells on incubation with Pgp and BCRP antibodies and a reduction in those on incubation with MRP1 antibodies. This directly indicates that tomoxifen binds to Pgp, BCRP, and MRP1, which inevitably results in a decrease in the intracellular concentration of the antiestrogen available for the interaction with other cellular targets, including that with estrogen receptors. The authors consider that there is every reason to consider Pgp, BCRP, and MRP1 as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer with the positive estrogen receptor status.https://ojrs.abvpress.ru/ojrs/article/view/136tamoxifenmultidrug resistance proteinspgpmrp1bcrpbreast cancerpredictive markers
spellingShingle T. A. Bogush
E. A. Dudko
E. A. Bogush
B. E. Polotsky
S. A. Tyulyandin
M. I. Davydov
The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
Опухоли женской репродуктивной системы
tamoxifen
multidrug resistance proteins
pgp
mrp1
bcrp
breast cancer
predictive markers
title The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
title_full The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
title_fullStr The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
title_full_unstemmed The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
title_short The multidrug resistance proteins Pgp, MRP, and BCRP as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
title_sort multidrug resistance proteins pgp mrp and bcrp as markers for lowering the efficacy of tamoxifen in the treatment of breast cancer
topic tamoxifen
multidrug resistance proteins
pgp
mrp1
bcrp
breast cancer
predictive markers
url https://ojrs.abvpress.ru/ojrs/article/view/136
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