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The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies
Understanding cell responses to the topography they are interacting with has a key role in designing surfaces due to the distinctiveness in the responses of different cell types. Thus far, a variety of surface textures have been fabricated, and the cellular responses of diversified cell lines to the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070382/ https://www.ncbi.nlm.nih.gov/pubmed/35531028 http://dx.doi.org/10.1039/c9ra03783g |
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author | Yaşayan, Gökçen Orun, Oya Mega Tiber, Pınar Rožman, Veronika Koçyiğit Sevinç, Sevgi |
author_facet | Yaşayan, Gökçen Orun, Oya Mega Tiber, Pınar Rožman, Veronika Koçyiğit Sevinç, Sevgi |
author_sort | Yaşayan, Gökçen |
collection | PubMed |
description | Understanding cell responses to the topography they are interacting with has a key role in designing surfaces due to the distinctiveness in the responses of different cell types. Thus far, a variety of surface textures have been fabricated, and the cellular responses of diversified cell lines to the surface textures have been assessed together with surface chemistry. However, the results reported in the literature are contradictory, and also not in-depth for inferring the relevance between cells, surface chemistry, and surface topography. Starting from this point of view, we focused on fabricating surfaces having extracellular matrix-like surface patterns and investigated the influence of patterning on human ovarian cancer cells. In this study, hemispherical protrusion-shaped, nanotextured surfaces were prepared via colloidal lithography and polymer casting methods using monolayer templates prepared from 280 nm, 210 nm, and 99 nm polystyrene particles and polydimethylsiloxane moulds. Then, the surface textures were transferred to biocompatible polycaprolactone films. After the characterisation of the surfaces via atomic force microscopy, X-ray photoelectron spectroscopy, and contact angle measurements, the cellular response to topography was evaluated by cell attachment, viability, and apoptosis studies. The results were compared with non-textured surfaces and control plate wells. The results showed that human ovarian cancer cell attachment increased with nanotexturing, which suggests that nanotexturing may be a promising approach for cancer cell modulation, and may have the potential to introduce new strategies for cancer treatment. |
format | Online Article Text |
id | pubmed-9070382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90703822022-05-05 The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies Yaşayan, Gökçen Orun, Oya Mega Tiber, Pınar Rožman, Veronika Koçyiğit Sevinç, Sevgi RSC Adv Chemistry Understanding cell responses to the topography they are interacting with has a key role in designing surfaces due to the distinctiveness in the responses of different cell types. Thus far, a variety of surface textures have been fabricated, and the cellular responses of diversified cell lines to the surface textures have been assessed together with surface chemistry. However, the results reported in the literature are contradictory, and also not in-depth for inferring the relevance between cells, surface chemistry, and surface topography. Starting from this point of view, we focused on fabricating surfaces having extracellular matrix-like surface patterns and investigated the influence of patterning on human ovarian cancer cells. In this study, hemispherical protrusion-shaped, nanotextured surfaces were prepared via colloidal lithography and polymer casting methods using monolayer templates prepared from 280 nm, 210 nm, and 99 nm polystyrene particles and polydimethylsiloxane moulds. Then, the surface textures were transferred to biocompatible polycaprolactone films. After the characterisation of the surfaces via atomic force microscopy, X-ray photoelectron spectroscopy, and contact angle measurements, the cellular response to topography was evaluated by cell attachment, viability, and apoptosis studies. The results were compared with non-textured surfaces and control plate wells. The results showed that human ovarian cancer cell attachment increased with nanotexturing, which suggests that nanotexturing may be a promising approach for cancer cell modulation, and may have the potential to introduce new strategies for cancer treatment. The Royal Society of Chemistry 2019-08-19 /pmc/articles/PMC9070382/ /pubmed/35531028 http://dx.doi.org/10.1039/c9ra03783g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Yaşayan, Gökçen Orun, Oya Mega Tiber, Pınar Rožman, Veronika Koçyiğit Sevinç, Sevgi The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title | The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title_full | The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title_fullStr | The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title_full_unstemmed | The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title_short | The interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
title_sort | interactions of human ovarian cancer cells and nanotextured surfaces: cell attachment, viability and apoptosis studies |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070382/ https://www.ncbi.nlm.nih.gov/pubmed/35531028 http://dx.doi.org/10.1039/c9ra03783g |
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