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Gene expression analysis in scars treated with silicone cream: a case series
BACKGROUND: In contrast to fetal scar tissue, adult scar tissue presents with visible scarring. Topical silicone creams have been shown to improve the appearance of scars. This case series compares the genetic expression of post-surgical scar tissues that received topical scar treatment with silicon...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755861/ https://www.ncbi.nlm.nih.gov/pubmed/31565401 http://dx.doi.org/10.1177/2059513119868345 |
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author | Kikuchi, Robin Khalil, Abdullah J Zoumalan, Christopher I |
author_facet | Kikuchi, Robin Khalil, Abdullah J Zoumalan, Christopher I |
author_sort | Kikuchi, Robin |
collection | PubMed |
description | BACKGROUND: In contrast to fetal scar tissue, adult scar tissue presents with visible scarring. Topical silicone creams have been shown to improve the appearance of scars. This case series compares the genetic expression of post-surgical scar tissues that received topical scar treatment with silicone cream, SKN2017B, or no treatment. SKN2017B is a recently formulated silicone-based scar cream that contains selective synthetic recombinant human growth factors, hyaluronic acid, and vitamin C. We hypothesise that scars treated with silicone-based scar creams have a more favourable genetic expression resembling a well-healing scar. METHODS: Women who had undergone an abdominoplasty were included in this investigation and randomly assigned to treat part of the scar with topical silicone, another part with SKN2017B, and to leave a third part untreated. After four weeks, punch biopsies were taken and the RNA sequenced. Healthy abdominal skin was biopsied as baseline data. Genes of interest were identified and median values were calculated for the samples. RESULTS: SKN2107B-treated scars demonstrated the lowest collagen type I to collagen type III ratio. Other key genes of interest in wound healing showed the lowest (favourable) expression of fibroblast activation protein alpha, lysyl oxidase and cartilage oligomeric matrix protein; the highest (favourable) expression of fibronectin type III domain containing 1 and matrix metallopeptidase 9 were found in scars treated with SKN2017B. CONCLUSION: The results of this small case series demonstrate a trend that those scars treated with topical silicone cream, notably SKN2017B, display the most favourable gene expression for wound healing. |
format | Online Article Text |
id | pubmed-6755861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67558612019-09-27 Gene expression analysis in scars treated with silicone cream: a case series Kikuchi, Robin Khalil, Abdullah J Zoumalan, Christopher I Scars Burn Heal Case Report BACKGROUND: In contrast to fetal scar tissue, adult scar tissue presents with visible scarring. Topical silicone creams have been shown to improve the appearance of scars. This case series compares the genetic expression of post-surgical scar tissues that received topical scar treatment with silicone cream, SKN2017B, or no treatment. SKN2017B is a recently formulated silicone-based scar cream that contains selective synthetic recombinant human growth factors, hyaluronic acid, and vitamin C. We hypothesise that scars treated with silicone-based scar creams have a more favourable genetic expression resembling a well-healing scar. METHODS: Women who had undergone an abdominoplasty were included in this investigation and randomly assigned to treat part of the scar with topical silicone, another part with SKN2017B, and to leave a third part untreated. After four weeks, punch biopsies were taken and the RNA sequenced. Healthy abdominal skin was biopsied as baseline data. Genes of interest were identified and median values were calculated for the samples. RESULTS: SKN2107B-treated scars demonstrated the lowest collagen type I to collagen type III ratio. Other key genes of interest in wound healing showed the lowest (favourable) expression of fibroblast activation protein alpha, lysyl oxidase and cartilage oligomeric matrix protein; the highest (favourable) expression of fibronectin type III domain containing 1 and matrix metallopeptidase 9 were found in scars treated with SKN2017B. CONCLUSION: The results of this small case series demonstrate a trend that those scars treated with topical silicone cream, notably SKN2017B, display the most favourable gene expression for wound healing. SAGE Publications 2019-08-21 /pmc/articles/PMC6755861/ /pubmed/31565401 http://dx.doi.org/10.1177/2059513119868345 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Kikuchi, Robin Khalil, Abdullah J Zoumalan, Christopher I Gene expression analysis in scars treated with silicone cream: a case series |
title | Gene expression analysis in scars treated with silicone cream: a case
series |
title_full | Gene expression analysis in scars treated with silicone cream: a case
series |
title_fullStr | Gene expression analysis in scars treated with silicone cream: a case
series |
title_full_unstemmed | Gene expression analysis in scars treated with silicone cream: a case
series |
title_short | Gene expression analysis in scars treated with silicone cream: a case
series |
title_sort | gene expression analysis in scars treated with silicone cream: a case
series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755861/ https://www.ncbi.nlm.nih.gov/pubmed/31565401 http://dx.doi.org/10.1177/2059513119868345 |
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