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Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment

Pancreatic cancer is one of the deadliest types of cancer, with a five-year survival rate of only 10%. Nanotechnology offers a novel perspective to treat such deadly cancers through their incorporation into radiotherapy and chemotherapy. However, the interaction of nanoparticles (NPs) with cancer ce...

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Autores principales: Alhussan, Abdulaziz, Bromma, Kyle, Bozdoğan, Ece Pinar Demirci, Metcalfe, Andrew, Karasinska, Joanna, Beckham, Wayne, Alexander, Abraham S., Renouf, Daniel J., Schaeffer, David F., Chithrani, Devika B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161808/
https://www.ncbi.nlm.nih.gov/pubmed/34073974
http://dx.doi.org/10.3390/curroncol28030183
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author Alhussan, Abdulaziz
Bromma, Kyle
Bozdoğan, Ece Pinar Demirci
Metcalfe, Andrew
Karasinska, Joanna
Beckham, Wayne
Alexander, Abraham S.
Renouf, Daniel J.
Schaeffer, David F.
Chithrani, Devika B.
author_facet Alhussan, Abdulaziz
Bromma, Kyle
Bozdoğan, Ece Pinar Demirci
Metcalfe, Andrew
Karasinska, Joanna
Beckham, Wayne
Alexander, Abraham S.
Renouf, Daniel J.
Schaeffer, David F.
Chithrani, Devika B.
author_sort Alhussan, Abdulaziz
collection PubMed
description Pancreatic cancer is one of the deadliest types of cancer, with a five-year survival rate of only 10%. Nanotechnology offers a novel perspective to treat such deadly cancers through their incorporation into radiotherapy and chemotherapy. However, the interaction of nanoparticles (NPs) with cancer cells and with other major cell types within the pancreatic tumor microenvironment (TME) is yet to be understood. Therefore, our goal is to shed light on the dynamics of NPs within a TME of pancreatic origin. In addition to cancer cells, normal fibroblasts (NFs) and cancer-associated fibroblasts (CAFs) were examined in this study due to their important yet opposite roles of suppressing tumor growth and promoting tumor growth, respectively. Gold nanoparticles were used as the model NP system due to their biocompatibility and physical and chemical proprieties, and their dynamics were studied both quantitatively and qualitatively in vitro and in vivo. The in vitro studies revealed that both cancer cells and CAFs take up 50% more NPs compared to NFs. Most importantly, they all managed to retain 70–80% of NPs over a 24-h time period. Uptake and retention of NPs within an in vivo environment was also consistent with in vitro results. This study shows the paradigm-changing potential of NPs to combat the disease.
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spelling pubmed-81618082021-05-29 Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment Alhussan, Abdulaziz Bromma, Kyle Bozdoğan, Ece Pinar Demirci Metcalfe, Andrew Karasinska, Joanna Beckham, Wayne Alexander, Abraham S. Renouf, Daniel J. Schaeffer, David F. Chithrani, Devika B. Curr Oncol Article Pancreatic cancer is one of the deadliest types of cancer, with a five-year survival rate of only 10%. Nanotechnology offers a novel perspective to treat such deadly cancers through their incorporation into radiotherapy and chemotherapy. However, the interaction of nanoparticles (NPs) with cancer cells and with other major cell types within the pancreatic tumor microenvironment (TME) is yet to be understood. Therefore, our goal is to shed light on the dynamics of NPs within a TME of pancreatic origin. In addition to cancer cells, normal fibroblasts (NFs) and cancer-associated fibroblasts (CAFs) were examined in this study due to their important yet opposite roles of suppressing tumor growth and promoting tumor growth, respectively. Gold nanoparticles were used as the model NP system due to their biocompatibility and physical and chemical proprieties, and their dynamics were studied both quantitatively and qualitatively in vitro and in vivo. The in vitro studies revealed that both cancer cells and CAFs take up 50% more NPs compared to NFs. Most importantly, they all managed to retain 70–80% of NPs over a 24-h time period. Uptake and retention of NPs within an in vivo environment was also consistent with in vitro results. This study shows the paradigm-changing potential of NPs to combat the disease. MDPI 2021-05-24 /pmc/articles/PMC8161808/ /pubmed/34073974 http://dx.doi.org/10.3390/curroncol28030183 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alhussan, Abdulaziz
Bromma, Kyle
Bozdoğan, Ece Pinar Demirci
Metcalfe, Andrew
Karasinska, Joanna
Beckham, Wayne
Alexander, Abraham S.
Renouf, Daniel J.
Schaeffer, David F.
Chithrani, Devika B.
Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title_full Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title_fullStr Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title_full_unstemmed Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title_short Investigation of Nano-Bio Interactions within a Pancreatic Tumor Microenvironment for the Advancement of Nanomedicine in Cancer Treatment
title_sort investigation of nano-bio interactions within a pancreatic tumor microenvironment for the advancement of nanomedicine in cancer treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161808/
https://www.ncbi.nlm.nih.gov/pubmed/34073974
http://dx.doi.org/10.3390/curroncol28030183
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