Cargando…
Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells
Cancer cells can take up gold nanoparticles of different morphologies. These particles interact with the plasma membrane and often travel to intracellular organelles. Among organelles, the nucleus is especially susceptible to the damage that is inflicted by gold nanoparticles. Located inside the nuc...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998265/ https://www.ncbi.nlm.nih.gov/pubmed/29942378 http://dx.doi.org/10.5772/62337 |
_version_ | 1783331212417302528 |
---|---|
author | Kodiha, Mohamed Mahboubi, Hicham Maysinger, Dusica Stochaj, Ursula |
author_facet | Kodiha, Mohamed Mahboubi, Hicham Maysinger, Dusica Stochaj, Ursula |
author_sort | Kodiha, Mohamed |
collection | PubMed |
description | Cancer cells can take up gold nanoparticles of different morphologies. These particles interact with the plasma membrane and often travel to intracellular organelles. Among organelles, the nucleus is especially susceptible to the damage that is inflicted by gold nanoparticles. Located inside the nucleus, nucleoli are specialized compartments that transcribe ribosomal RNA genes, produce ribosomes and function as cellular stress sensors. Nucleoli are particularly prone to gold nanoparticle-induced injury. As such, small spherical gold nanoparticles and gold nanoflowers interfere with the transcription of ribosomal DNA. However, the underlying mechanisms are not fully understood. In this study, we examined the effects of gold nanoparticles on nucleolar proteins that are critical to ribosome biogenesis and other cellular functions. We show that B23/nucleophosmin, a nucleolar protein that is tightly linked to cancer, is significantly affected by gold nanoparticles. Furthermore, gold nanoparticles impinge on the cellular stress response, as they reduce the abundance of the molecular chaperone hsp70 and O-GlcNAc modified proteins in the nucleus and nucleoli. Together, our studies set the stage for the development of nanomedicines that target the nucleolus to eradicate proliferating cancer cells. |
format | Online Article Text |
id | pubmed-5998265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59982652018-06-25 Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells Kodiha, Mohamed Mahboubi, Hicham Maysinger, Dusica Stochaj, Ursula Nanobiomedicine (Rij) Nanobiomedicine Cancer cells can take up gold nanoparticles of different morphologies. These particles interact with the plasma membrane and often travel to intracellular organelles. Among organelles, the nucleus is especially susceptible to the damage that is inflicted by gold nanoparticles. Located inside the nucleus, nucleoli are specialized compartments that transcribe ribosomal RNA genes, produce ribosomes and function as cellular stress sensors. Nucleoli are particularly prone to gold nanoparticle-induced injury. As such, small spherical gold nanoparticles and gold nanoflowers interfere with the transcription of ribosomal DNA. However, the underlying mechanisms are not fully understood. In this study, we examined the effects of gold nanoparticles on nucleolar proteins that are critical to ribosome biogenesis and other cellular functions. We show that B23/nucleophosmin, a nucleolar protein that is tightly linked to cancer, is significantly affected by gold nanoparticles. Furthermore, gold nanoparticles impinge on the cellular stress response, as they reduce the abundance of the molecular chaperone hsp70 and O-GlcNAc modified proteins in the nucleus and nucleoli. Together, our studies set the stage for the development of nanomedicines that target the nucleolus to eradicate proliferating cancer cells. SAGE Publications 2016-01-01 /pmc/articles/PMC5998265/ /pubmed/29942378 http://dx.doi.org/10.5772/62337 Text en © 2016 Author(s). Licensee InTech. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nanobiomedicine Kodiha, Mohamed Mahboubi, Hicham Maysinger, Dusica Stochaj, Ursula Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title | Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title_full | Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title_fullStr | Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title_full_unstemmed | Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title_short | Gold Nanoparticles Impinge on Nucleoli and the Stress Response in MCF7 Breast Cancer Cells |
title_sort | gold nanoparticles impinge on nucleoli and the stress response in mcf7 breast cancer cells |
topic | Nanobiomedicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998265/ https://www.ncbi.nlm.nih.gov/pubmed/29942378 http://dx.doi.org/10.5772/62337 |
work_keys_str_mv | AT kodihamohamed goldnanoparticlesimpingeonnucleoliandthestressresponseinmcf7breastcancercells AT mahboubihicham goldnanoparticlesimpingeonnucleoliandthestressresponseinmcf7breastcancercells AT maysingerdusica goldnanoparticlesimpingeonnucleoliandthestressresponseinmcf7breastcancercells AT stochajursula goldnanoparticlesimpingeonnucleoliandthestressresponseinmcf7breastcancercells |