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LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate
Methotrexate (MTX) is a folate analogue antimetabolite widely used for the treatment of rheumatoid arthritis and cancer. A number of studies have shown that MTX delivered via nanoparticle carriers is more potent against cancer cells than free MTX, a phenomenon attributed to higher cellular uptake of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977166/ https://www.ncbi.nlm.nih.gov/pubmed/31993584 http://dx.doi.org/10.1016/j.ijpx.2019.100036 |
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author | Al-Natour, Mohammad Ahmad Alazzo, Ali Ghaemmaghami, Amir M. Kim, Dong-Hyun Alexander, Cameron |
author_facet | Al-Natour, Mohammad Ahmad Alazzo, Ali Ghaemmaghami, Amir M. Kim, Dong-Hyun Alexander, Cameron |
author_sort | Al-Natour, Mohammad Ahmad |
collection | PubMed |
description | Methotrexate (MTX) is a folate analogue antimetabolite widely used for the treatment of rheumatoid arthritis and cancer. A number of studies have shown that MTX delivered via nanoparticle carriers is more potent against cancer cells than free MTX, a phenomenon attributed to higher cellular uptake of the particles compared to the saturable folate receptor pathway. In this study, a cell-based global metabolic profiling approach was applied to study the effects of MTX in both free drug form and when encapsulated in -poly(lactide-co-glycolide) (PLGA) nanoparticles on a cancer cell line, A549, and also on human-like THP-1 macrophages. The results showed that MTX loaded nanoparticles had less impact on the macrophages than free MTX, and the effects on macrophages were limited to changes in nucleotide metabolism and suppression of the tricarboxylic acid cycle, whereas free MTX also led to a drop in glycolytic activity and impairment in redox homeostasis. In contrast, MTX loaded nanoparticles showed a greater impact on A549 cells than the free drug, which was in accord with studies in other cell lines in prior literature with MTX-carrier nanoparticles. |
format | Online Article Text |
id | pubmed-6977166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-69771662020-01-28 LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate Al-Natour, Mohammad Ahmad Alazzo, Ali Ghaemmaghami, Amir M. Kim, Dong-Hyun Alexander, Cameron Int J Pharm X Special section on SFNano 2018 meeting: Nanomedicine - from particle design to applications; edited by Dr. Nathalie Mignet, Dr. Chantal Pichon and Dr. Marie-Pierre Rols Methotrexate (MTX) is a folate analogue antimetabolite widely used for the treatment of rheumatoid arthritis and cancer. A number of studies have shown that MTX delivered via nanoparticle carriers is more potent against cancer cells than free MTX, a phenomenon attributed to higher cellular uptake of the particles compared to the saturable folate receptor pathway. In this study, a cell-based global metabolic profiling approach was applied to study the effects of MTX in both free drug form and when encapsulated in -poly(lactide-co-glycolide) (PLGA) nanoparticles on a cancer cell line, A549, and also on human-like THP-1 macrophages. The results showed that MTX loaded nanoparticles had less impact on the macrophages than free MTX, and the effects on macrophages were limited to changes in nucleotide metabolism and suppression of the tricarboxylic acid cycle, whereas free MTX also led to a drop in glycolytic activity and impairment in redox homeostasis. In contrast, MTX loaded nanoparticles showed a greater impact on A549 cells than the free drug, which was in accord with studies in other cell lines in prior literature with MTX-carrier nanoparticles. Elsevier 2019-11-12 /pmc/articles/PMC6977166/ /pubmed/31993584 http://dx.doi.org/10.1016/j.ijpx.2019.100036 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Special section on SFNano 2018 meeting: Nanomedicine - from particle design to applications; edited by Dr. Nathalie Mignet, Dr. Chantal Pichon and Dr. Marie-Pierre Rols Al-Natour, Mohammad Ahmad Alazzo, Ali Ghaemmaghami, Amir M. Kim, Dong-Hyun Alexander, Cameron LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title | LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title_full | LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title_fullStr | LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title_full_unstemmed | LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title_short | LC-MS metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
title_sort | lc-ms metabolomics comparisons of cancer cell and macrophage responses to methotrexate and polymer-encapsulated methotrexate |
topic | Special section on SFNano 2018 meeting: Nanomedicine - from particle design to applications; edited by Dr. Nathalie Mignet, Dr. Chantal Pichon and Dr. Marie-Pierre Rols |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977166/ https://www.ncbi.nlm.nih.gov/pubmed/31993584 http://dx.doi.org/10.1016/j.ijpx.2019.100036 |
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