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MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells

MicroRNAs (miRNAs) are single-stranded, non-coding, 19–25 nucleotide RNA molecules that have been observed to be dysregulated in many diseases including cancer. miRNAs have been known to play an important role in cellular proliferation, differentiation, migration, apoptosis, survival, and morphogene...

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Autores principales: Chaudhari, Ramesh, Nasra, Simran, Meghani, Nikita, Kumar, Ashutosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933417/
https://www.ncbi.nlm.nih.gov/pubmed/35304514
http://dx.doi.org/10.1038/s41598-022-08185-1
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author Chaudhari, Ramesh
Nasra, Simran
Meghani, Nikita
Kumar, Ashutosh
author_facet Chaudhari, Ramesh
Nasra, Simran
Meghani, Nikita
Kumar, Ashutosh
author_sort Chaudhari, Ramesh
collection PubMed
description MicroRNAs (miRNAs) are single-stranded, non-coding, 19–25 nucleotide RNA molecules that have been observed to be dysregulated in many diseases including cancer. miRNAs have been known to play an important role in cellular proliferation, differentiation, migration, apoptosis, survival, and morphogenesis. Breast cancer is heterogeneous in nature and contributed extensively to the increased mortality rate. miRNA can either be tumor-suppressive or oncogenic in nature. The level of expression of miRNA changes according to the subtypes of cancer and the mutation responsible for different cancers. miRNA mimicry or inhibition are emerging possible therapies to maintain the level of miRNA inside the cells. In order to have proper miRNA mimicry, the major hurdle is to deliver the miRNA mimics at the site of tumor. Metallic nanoparticles with modified surface can be used to solve the problem of miRNA delivery. MiR-206 is reported to be down-regulated in Luminal-A type of breast cancer. In the current manuscript, we aim to modify the surface of gold-nanoparticles (AuNPs) with PEG moiety and allow miRNA to attach to it. The fabricated nano-complex, not only delivered miR-206 but also caused cell death in MCF-7 by arresting cells in the G0-G1 phase and inducing apoptosis by downregulating NOTCH 3.
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spelling pubmed-89334172022-03-28 MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells Chaudhari, Ramesh Nasra, Simran Meghani, Nikita Kumar, Ashutosh Sci Rep Article MicroRNAs (miRNAs) are single-stranded, non-coding, 19–25 nucleotide RNA molecules that have been observed to be dysregulated in many diseases including cancer. miRNAs have been known to play an important role in cellular proliferation, differentiation, migration, apoptosis, survival, and morphogenesis. Breast cancer is heterogeneous in nature and contributed extensively to the increased mortality rate. miRNA can either be tumor-suppressive or oncogenic in nature. The level of expression of miRNA changes according to the subtypes of cancer and the mutation responsible for different cancers. miRNA mimicry or inhibition are emerging possible therapies to maintain the level of miRNA inside the cells. In order to have proper miRNA mimicry, the major hurdle is to deliver the miRNA mimics at the site of tumor. Metallic nanoparticles with modified surface can be used to solve the problem of miRNA delivery. MiR-206 is reported to be down-regulated in Luminal-A type of breast cancer. In the current manuscript, we aim to modify the surface of gold-nanoparticles (AuNPs) with PEG moiety and allow miRNA to attach to it. The fabricated nano-complex, not only delivered miR-206 but also caused cell death in MCF-7 by arresting cells in the G0-G1 phase and inducing apoptosis by downregulating NOTCH 3. Nature Publishing Group UK 2022-03-18 /pmc/articles/PMC8933417/ /pubmed/35304514 http://dx.doi.org/10.1038/s41598-022-08185-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chaudhari, Ramesh
Nasra, Simran
Meghani, Nikita
Kumar, Ashutosh
MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title_full MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title_fullStr MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title_full_unstemmed MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title_short MiR-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
title_sort mir-206 conjugated gold nanoparticle based targeted therapy in breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933417/
https://www.ncbi.nlm.nih.gov/pubmed/35304514
http://dx.doi.org/10.1038/s41598-022-08185-1
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