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How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells
It was recently shown that it is possible to exploit the nanoparticle shape to selectively target endocytosis pathways found in cancer and not healthy cells. It is important to understand and compare the endocytosis pathways of nanoparticles in both cancer and healthy cells to restrict the healthy c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635177/ https://www.ncbi.nlm.nih.gov/pubmed/34976362 http://dx.doi.org/10.1039/d1sc04656j |
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author | Cong, Vu Thanh Tilley, Richard D. Sharbeen, George Phillips, Phoebe A. Gaus, Katharina Gooding, J. Justin |
author_facet | Cong, Vu Thanh Tilley, Richard D. Sharbeen, George Phillips, Phoebe A. Gaus, Katharina Gooding, J. Justin |
author_sort | Cong, Vu Thanh |
collection | PubMed |
description | It was recently shown that it is possible to exploit the nanoparticle shape to selectively target endocytosis pathways found in cancer and not healthy cells. It is important to understand and compare the endocytosis pathways of nanoparticles in both cancer and healthy cells to restrict the healthy cells from taking up anticancer drugs to help reduce the side effects for patients. Here, the clathrin-mediated endocytosis inhibitor, hydroxychloroquine, and the anticancer drug, doxorubicin, are loaded into the same mesoporous silica nanorods. The use of nanorods was found to restrict the uptake by healthy cells but allowed cancer cells to take up the nanorods via the macropinocytosis pathway. Furthermore, it is shown that the nanorods can selectively deliver doxorubicin to the nucleus of breast cancer cells and to the cytoplasm of pancreatic cancer cells. The dual-drug-loaded nanorods were able to selectively kill the breast cancer cells in the presence of healthy breast cells. This study opens exciting possibilities of targeting cancer cells based on the material shape rather than targeting antibodies. |
format | Online Article Text |
id | pubmed-8635177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86351772021-12-30 How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells Cong, Vu Thanh Tilley, Richard D. Sharbeen, George Phillips, Phoebe A. Gaus, Katharina Gooding, J. Justin Chem Sci Chemistry It was recently shown that it is possible to exploit the nanoparticle shape to selectively target endocytosis pathways found in cancer and not healthy cells. It is important to understand and compare the endocytosis pathways of nanoparticles in both cancer and healthy cells to restrict the healthy cells from taking up anticancer drugs to help reduce the side effects for patients. Here, the clathrin-mediated endocytosis inhibitor, hydroxychloroquine, and the anticancer drug, doxorubicin, are loaded into the same mesoporous silica nanorods. The use of nanorods was found to restrict the uptake by healthy cells but allowed cancer cells to take up the nanorods via the macropinocytosis pathway. Furthermore, it is shown that the nanorods can selectively deliver doxorubicin to the nucleus of breast cancer cells and to the cytoplasm of pancreatic cancer cells. The dual-drug-loaded nanorods were able to selectively kill the breast cancer cells in the presence of healthy breast cells. This study opens exciting possibilities of targeting cancer cells based on the material shape rather than targeting antibodies. The Royal Society of Chemistry 2021-11-18 /pmc/articles/PMC8635177/ /pubmed/34976362 http://dx.doi.org/10.1039/d1sc04656j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cong, Vu Thanh Tilley, Richard D. Sharbeen, George Phillips, Phoebe A. Gaus, Katharina Gooding, J. Justin How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title | How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title_full | How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title_fullStr | How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title_full_unstemmed | How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title_short | How to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
title_sort | how to exploit different endocytosis pathways to allow selective delivery of anticancer drugs to cancer cells over healthy cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635177/ https://www.ncbi.nlm.nih.gov/pubmed/34976362 http://dx.doi.org/10.1039/d1sc04656j |
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