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Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects
Metabolic reengineering using nanoparticle delivery represents an innovative therapeutic approach to normalizing the deregulation of cellular metabolism underlying many diseases, including cancer. Here, we demonstrated a unique and novel application to the treatment of malignancy using a short-chain...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598551/ https://www.ncbi.nlm.nih.gov/pubmed/28932113 http://dx.doi.org/10.2147/IJN.S135968 |
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author | Brody, Leigh P Sahuri-Arisoylu, Meliz Parkinson, James R Parkes, Harry G So, Po Wah Hajji, Nabil Thomas, E Louise Frost, Gary S Miller, Andrew D Bell, Jimmy D |
author_facet | Brody, Leigh P Sahuri-Arisoylu, Meliz Parkinson, James R Parkes, Harry G So, Po Wah Hajji, Nabil Thomas, E Louise Frost, Gary S Miller, Andrew D Bell, Jimmy D |
author_sort | Brody, Leigh P |
collection | PubMed |
description | Metabolic reengineering using nanoparticle delivery represents an innovative therapeutic approach to normalizing the deregulation of cellular metabolism underlying many diseases, including cancer. Here, we demonstrated a unique and novel application to the treatment of malignancy using a short-chain fatty acid (SCFA)-encapsulated lipid-based delivery system – liposome-encapsulated acetate nanoparticles for cancer applications (LITA-CAN). We assessed chronic in vivo administration of our nanoparticle in three separate murine models of colorectal cancer. We demonstrated a substantial reduction in tumor growth in the xenograft model of colorectal cancer cell lines HT-29, HCT-116 p53+/+ and HCT-116 p53−/−. Nanoparticle-induced reductions in histone deacetylase gene expression indicated a potential mechanism for these anti-proliferative effects. Together, these results indicated that LITA-CAN could be used as an effective direct or adjunct therapy to treat malignant transformation in vivo. |
format | Online Article Text |
id | pubmed-5598551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55985512017-09-20 Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects Brody, Leigh P Sahuri-Arisoylu, Meliz Parkinson, James R Parkes, Harry G So, Po Wah Hajji, Nabil Thomas, E Louise Frost, Gary S Miller, Andrew D Bell, Jimmy D Int J Nanomedicine Original Research Metabolic reengineering using nanoparticle delivery represents an innovative therapeutic approach to normalizing the deregulation of cellular metabolism underlying many diseases, including cancer. Here, we demonstrated a unique and novel application to the treatment of malignancy using a short-chain fatty acid (SCFA)-encapsulated lipid-based delivery system – liposome-encapsulated acetate nanoparticles for cancer applications (LITA-CAN). We assessed chronic in vivo administration of our nanoparticle in three separate murine models of colorectal cancer. We demonstrated a substantial reduction in tumor growth in the xenograft model of colorectal cancer cell lines HT-29, HCT-116 p53+/+ and HCT-116 p53−/−. Nanoparticle-induced reductions in histone deacetylase gene expression indicated a potential mechanism for these anti-proliferative effects. Together, these results indicated that LITA-CAN could be used as an effective direct or adjunct therapy to treat malignant transformation in vivo. Dove Medical Press 2017-09-08 /pmc/articles/PMC5598551/ /pubmed/28932113 http://dx.doi.org/10.2147/IJN.S135968 Text en © 2017 Brody 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 Brody, Leigh P Sahuri-Arisoylu, Meliz Parkinson, James R Parkes, Harry G So, Po Wah Hajji, Nabil Thomas, E Louise Frost, Gary S Miller, Andrew D Bell, Jimmy D Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title | Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title_full | Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title_fullStr | Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title_full_unstemmed | Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title_short | Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
title_sort | cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598551/ https://www.ncbi.nlm.nih.gov/pubmed/28932113 http://dx.doi.org/10.2147/IJN.S135968 |
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