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Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells
Skin cancer or cutaneous carcinoma, is a pre-eminent global public health problem with no signs of plateauing in its incidence. As the most common treatments for skin cancer, surgical resection inevitably damages a patient’s appearance, and chemotherapy has many side effects. Thus, the main aim of t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981617/ https://www.ncbi.nlm.nih.gov/pubmed/29855618 http://dx.doi.org/10.1038/s41598-018-26749-y |
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author | Gan, Bee Koon Yong, Chean Yeah Ho, Kok Lian Omar, Abdul Rahman Alitheen, Noorjahan Banu Tan, Wen Siang |
author_facet | Gan, Bee Koon Yong, Chean Yeah Ho, Kok Lian Omar, Abdul Rahman Alitheen, Noorjahan Banu Tan, Wen Siang |
author_sort | Gan, Bee Koon |
collection | PubMed |
description | Skin cancer or cutaneous carcinoma, is a pre-eminent global public health problem with no signs of plateauing in its incidence. As the most common treatments for skin cancer, surgical resection inevitably damages a patient’s appearance, and chemotherapy has many side effects. Thus, the main aim of this study was to screen for a cell penetrating peptide (CPP) for the development of a targeting vector for skin cancer. In this study, we identified a CPP with the sequence NRPDSAQFWLHH from a phage displayed peptide library. This CPP targeted the human squamous carcinoma A431 cells through an interaction with the epidermal growth factor receptor (EGFr). Methyl-β-cyclodextrin (MβCD) and chlorpromazine hydrochloride (CPZ) inhibited the internalisation of the CPP into the A431 cells, suggesting the peptide entered the cells via clathrin-dependent endocytosis. The CPP displayed on hepatitis B virus-like nanoparticles (VLNPs) via the nanoglue successfully delivered the nanoparticles into A431 cells. The present study demonstrated that the novel CPP can serve as a ligand to target and deliver VLNPs into skin cancer cells. |
format | Online Article Text |
id | pubmed-5981617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59816172018-06-07 Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells Gan, Bee Koon Yong, Chean Yeah Ho, Kok Lian Omar, Abdul Rahman Alitheen, Noorjahan Banu Tan, Wen Siang Sci Rep Article Skin cancer or cutaneous carcinoma, is a pre-eminent global public health problem with no signs of plateauing in its incidence. As the most common treatments for skin cancer, surgical resection inevitably damages a patient’s appearance, and chemotherapy has many side effects. Thus, the main aim of this study was to screen for a cell penetrating peptide (CPP) for the development of a targeting vector for skin cancer. In this study, we identified a CPP with the sequence NRPDSAQFWLHH from a phage displayed peptide library. This CPP targeted the human squamous carcinoma A431 cells through an interaction with the epidermal growth factor receptor (EGFr). Methyl-β-cyclodextrin (MβCD) and chlorpromazine hydrochloride (CPZ) inhibited the internalisation of the CPP into the A431 cells, suggesting the peptide entered the cells via clathrin-dependent endocytosis. The CPP displayed on hepatitis B virus-like nanoparticles (VLNPs) via the nanoglue successfully delivered the nanoparticles into A431 cells. The present study demonstrated that the novel CPP can serve as a ligand to target and deliver VLNPs into skin cancer cells. Nature Publishing Group UK 2018-05-31 /pmc/articles/PMC5981617/ /pubmed/29855618 http://dx.doi.org/10.1038/s41598-018-26749-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gan, Bee Koon Yong, Chean Yeah Ho, Kok Lian Omar, Abdul Rahman Alitheen, Noorjahan Banu Tan, Wen Siang Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title | Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title_full | Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title_fullStr | Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title_full_unstemmed | Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title_short | Targeted Delivery of Cell Penetrating Peptide Virus-like Nanoparticles to Skin Cancer Cells |
title_sort | targeted delivery of cell penetrating peptide virus-like nanoparticles to skin cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981617/ https://www.ncbi.nlm.nih.gov/pubmed/29855618 http://dx.doi.org/10.1038/s41598-018-26749-y |
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