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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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Detalles Bibliográficos
Autor principal: Evans, Ronise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
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.
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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
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