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Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells

Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization...

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Autores principales: Chung, Yuan-Chiang, Chang, Ching-Ming, Wei, Wan-Chen, Chang, Ting-Wei, Chang, King-Jen, Chao, Wei-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834501/
https://www.ncbi.nlm.nih.gov/pubmed/29500444
http://dx.doi.org/10.1038/s41598-018-22250-8
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author Chung, Yuan-Chiang
Chang, Ching-Ming
Wei, Wan-Chen
Chang, Ting-Wei
Chang, King-Jen
Chao, Wei-Ting
author_facet Chung, Yuan-Chiang
Chang, Ching-Ming
Wei, Wan-Chen
Chang, Ting-Wei
Chang, King-Jen
Chao, Wei-Ting
author_sort Chung, Yuan-Chiang
collection PubMed
description Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis.
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spelling pubmed-58345012018-03-05 Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells Chung, Yuan-Chiang Chang, Ching-Ming Wei, Wan-Chen Chang, Ting-Wei Chang, King-Jen Chao, Wei-Ting Sci Rep Article Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis. Nature Publishing Group UK 2018-03-02 /pmc/articles/PMC5834501/ /pubmed/29500444 http://dx.doi.org/10.1038/s41598-018-22250-8 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
Chung, Yuan-Chiang
Chang, Ching-Ming
Wei, Wan-Chen
Chang, Ting-Wei
Chang, King-Jen
Chao, Wei-Ting
Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title_full Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title_fullStr Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title_full_unstemmed Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title_short Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
title_sort metformin-induced caveolin-1 expression promotes t-dm1 drug efficacy in breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834501/
https://www.ncbi.nlm.nih.gov/pubmed/29500444
http://dx.doi.org/10.1038/s41598-018-22250-8
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