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Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer”
The major theme throughout this paper was solving the problem of multidrug resistance (MDR) in chemotherapeutic remediation for breast cancer patients by an aptamer-labeled hybrid nanoparticle to enhance selective delivery of siRNA into tumor cells and produce an enhanced knock-down of P-glycoprotei...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485932/ https://www.ncbi.nlm.nih.gov/pubmed/31032482 http://dx.doi.org/10.29245/2578-2967/2018/1.1103 |
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author | Evans, Ronise |
author_facet | Evans, Ronise |
author_sort | Evans, Ronise |
collection | PubMed |
description | The major theme throughout this paper was solving the problem of multidrug resistance (MDR) in chemotherapeutic remediation for breast cancer patients by an aptamer-labeled hybrid nanoparticle to enhance selective delivery of siRNA into tumor cells and produce an enhanced knock-down of P-glycoprotein (P-gp); which was detected mainly by western blot. The primary focus of this study was to know whether labeling nanoparticles with a cancer cell specific aptamer could enhance selective delivery of siRNA into tumor cells leading to enhanced knock-down of P-glycoprotein or P-gp as compared to non-labeled nanoparticles. The goal is to minimize cancerous gene expression by silencing its mRNA. Target specificity is not only key in completing this goal, but it is also necessary regarding, biodegradability, cytotoxicity and immune response. To accomplish this goal, the design methods had to be meticulous and carefully researched and applied. |
format | Online Article Text |
id | pubmed-6485932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64859322019-04-26 Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” Evans, Ronise J Cancer Treatment Diagn Article The major theme throughout this paper was solving the problem of multidrug resistance (MDR) in chemotherapeutic remediation for breast cancer patients by an aptamer-labeled hybrid nanoparticle to enhance selective delivery of siRNA into tumor cells and produce an enhanced knock-down of P-glycoprotein (P-gp); which was detected mainly by western blot. The primary focus of this study was to know whether labeling nanoparticles with a cancer cell specific aptamer could enhance selective delivery of siRNA into tumor cells leading to enhanced knock-down of P-glycoprotein or P-gp as compared to non-labeled nanoparticles. The goal is to minimize cancerous gene expression by silencing its mRNA. Target specificity is not only key in completing this goal, but it is also necessary regarding, biodegradability, cytotoxicity and immune response. To accomplish this goal, the design methods had to be meticulous and carefully researched and applied. 2017-12-07 2017 /pmc/articles/PMC6485932/ /pubmed/31032482 http://dx.doi.org/10.29245/2578-2967/2018/1.1103 Text en http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 International License. |
spellingShingle | Article Evans, Ronise Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title | Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title_full | Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title_fullStr | Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title_full_unstemmed | Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title_short | Commentary: “Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
title_sort | commentary: “aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer” |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485932/ https://www.ncbi.nlm.nih.gov/pubmed/31032482 http://dx.doi.org/10.29245/2578-2967/2018/1.1103 |
work_keys_str_mv | AT evansronise commentaryaptamerfunctionalizedhybridnanoparticleforthetreatmentofbreastcancer |