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Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia
Today, the therapeutic efficacy of cancer is restricted by the heterogeneity of the response of tumor cells to chemotherapeutic drugs. Since those therapies are also associated with severe side effects in nontarget organs, the application of drugs in combination with nanocarriers for targeted therap...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745830/ https://www.ncbi.nlm.nih.gov/pubmed/26893557 http://dx.doi.org/10.2147/IJN.S94384 |
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author | Stapf, Marcus Pömpner, Nadine Teichgräber, Ulf Hilger, Ingrid |
author_facet | Stapf, Marcus Pömpner, Nadine Teichgräber, Ulf Hilger, Ingrid |
author_sort | Stapf, Marcus |
collection | PubMed |
description | Today, the therapeutic efficacy of cancer is restricted by the heterogeneity of the response of tumor cells to chemotherapeutic drugs. Since those therapies are also associated with severe side effects in nontarget organs, the application of drugs in combination with nanocarriers for targeted therapy has been suggested. Here, we sought to assess whether the coupling of methotrexate (MTX) to magnetic nanoparticles (MNP) could serve as a valuable tool to circumvent the heterogeneity of tumor cell response to MTX by the combined treatment with hyperthermia. To this end, we investigated five breast cancer cell lines of different origin and with different mutational statuses, as well as a bladder cancer cell line in terms of their response to exposure to MTX as a free drug or after its coupling to MNP as well as in presence/absence of hyperthermia. We also assessed whether the effects could be connected to the cell line-specific expression of proteins related to the uptake and efflux of MTX and MNP. Our results revealed a very heterogeneous and cell line-dependent response to an exposure with MTX-coupled MNP (MTX–MNP), which was almost comparable to the efficacy of free MTX in the same cell line. Moreover, a cell line-specific and preferential uptake of MTX–MNP compared with MNP alone was found (probably by receptor-mediated endocytosis), agreeing with the observed cytotoxic effects. Opposed to this, the expression pattern of several cell membrane transport proteins noted for MTX uptake and efflux was only by tendency in agreement with the cellular toxicity of MTX–MNP in different cell lines. Higher cytotoxic effects were achieved by exposing cells to a combination of MTX–MNP and hyperthermal treatment, compared with MTX or thermo-therapy alone. However, the heterogeneity in the response of the tumor cell lines to MTX could not be completely abolished – even after its combination with MNP and/or hyperthermia – and the application of higher thermal dosages might be necessary. |
format | Online Article Text |
id | pubmed-4745830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47458302016-02-18 Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia Stapf, Marcus Pömpner, Nadine Teichgräber, Ulf Hilger, Ingrid Int J Nanomedicine Original Research Today, the therapeutic efficacy of cancer is restricted by the heterogeneity of the response of tumor cells to chemotherapeutic drugs. Since those therapies are also associated with severe side effects in nontarget organs, the application of drugs in combination with nanocarriers for targeted therapy has been suggested. Here, we sought to assess whether the coupling of methotrexate (MTX) to magnetic nanoparticles (MNP) could serve as a valuable tool to circumvent the heterogeneity of tumor cell response to MTX by the combined treatment with hyperthermia. To this end, we investigated five breast cancer cell lines of different origin and with different mutational statuses, as well as a bladder cancer cell line in terms of their response to exposure to MTX as a free drug or after its coupling to MNP as well as in presence/absence of hyperthermia. We also assessed whether the effects could be connected to the cell line-specific expression of proteins related to the uptake and efflux of MTX and MNP. Our results revealed a very heterogeneous and cell line-dependent response to an exposure with MTX-coupled MNP (MTX–MNP), which was almost comparable to the efficacy of free MTX in the same cell line. Moreover, a cell line-specific and preferential uptake of MTX–MNP compared with MNP alone was found (probably by receptor-mediated endocytosis), agreeing with the observed cytotoxic effects. Opposed to this, the expression pattern of several cell membrane transport proteins noted for MTX uptake and efflux was only by tendency in agreement with the cellular toxicity of MTX–MNP in different cell lines. Higher cytotoxic effects were achieved by exposing cells to a combination of MTX–MNP and hyperthermal treatment, compared with MTX or thermo-therapy alone. However, the heterogeneity in the response of the tumor cell lines to MTX could not be completely abolished – even after its combination with MNP and/or hyperthermia – and the application of higher thermal dosages might be necessary. Dove Medical Press 2016-02-04 /pmc/articles/PMC4745830/ /pubmed/26893557 http://dx.doi.org/10.2147/IJN.S94384 Text en © 2016 Stapf et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Stapf, Marcus Pömpner, Nadine Teichgräber, Ulf Hilger, Ingrid Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title | Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title_full | Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title_fullStr | Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title_full_unstemmed | Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title_short | Heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
title_sort | heterogeneous response of different tumor cell lines to methotrexate-coupled nanoparticles in presence of hyperthermia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745830/ https://www.ncbi.nlm.nih.gov/pubmed/26893557 http://dx.doi.org/10.2147/IJN.S94384 |
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