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Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas
To investigate the relationship between keratoacanthoma (KA) and squamous cell carcinoma (SCC), cytokine mRNA in 12 KA and eight SCC were compared. Normal skin was also studied. Reverse transcription polymerase chain reaction (RT-PCR) was used to quantitate mRNA in each sample utilizing DNA standard...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363088/ https://www.ncbi.nlm.nih.gov/pubmed/10408389 http://dx.doi.org/10.1038/sj.bjc.6690552 |
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author | Lowes, M A Bishop, G A Cooke, B E Barnetson, R StC Halliday, G M |
author_facet | Lowes, M A Bishop, G A Cooke, B E Barnetson, R StC Halliday, G M |
author_sort | Lowes, M A |
collection | PubMed |
description | To investigate the relationship between keratoacanthoma (KA) and squamous cell carcinoma (SCC), cytokine mRNA in 12 KA and eight SCC were compared. Normal skin was also studied. Reverse transcription polymerase chain reaction (RT-PCR) was used to quantitate mRNA in each sample utilizing DNA standards. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as an internal control, and CD3δ as an indication of the T-cell infiltrate. KAs showed a significant increase in interleukin (IL)-10, and a decrease in granulocyte macrophage colony-stimulating factor (GM-CSF) mRNA compared to SCCs. CD3δ mRNA was also increased in the KAs. There was no difference between KAs and SCCs in expression of lymphotoxin-α, IL-2, interferon-γ (IFN-γ), IL-13, transforming growth factor-β (TGF-β), or the pro-inflammatory cytokines IL-8 or tumour necrosis factor-α (TNF-α). These results indicate that KAs spontaneously resolve in an immunosuppressive environment. KAs grow rapidly over a period of weeks and then involute. It is possible that a suppressed immune response enables unimpeded growth and that the KA cells rapidly undergo the finite number of cell divisions of which they are capable, and then die without reaching immortality. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2363088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23630882009-09-10 Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas Lowes, M A Bishop, G A Cooke, B E Barnetson, R StC Halliday, G M Br J Cancer Regular Article To investigate the relationship between keratoacanthoma (KA) and squamous cell carcinoma (SCC), cytokine mRNA in 12 KA and eight SCC were compared. Normal skin was also studied. Reverse transcription polymerase chain reaction (RT-PCR) was used to quantitate mRNA in each sample utilizing DNA standards. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as an internal control, and CD3δ as an indication of the T-cell infiltrate. KAs showed a significant increase in interleukin (IL)-10, and a decrease in granulocyte macrophage colony-stimulating factor (GM-CSF) mRNA compared to SCCs. CD3δ mRNA was also increased in the KAs. There was no difference between KAs and SCCs in expression of lymphotoxin-α, IL-2, interferon-γ (IFN-γ), IL-13, transforming growth factor-β (TGF-β), or the pro-inflammatory cytokines IL-8 or tumour necrosis factor-α (TNF-α). These results indicate that KAs spontaneously resolve in an immunosuppressive environment. KAs grow rapidly over a period of weeks and then involute. It is possible that a suppressed immune response enables unimpeded growth and that the KA cells rapidly undergo the finite number of cell divisions of which they are capable, and then die without reaching immortality. © 1999 Cancer Research Campaign Nature Publishing Group 1999-07 /pmc/articles/PMC2363088/ /pubmed/10408389 http://dx.doi.org/10.1038/sj.bjc.6690552 Text en Copyright © 1999 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Lowes, M A Bishop, G A Cooke, B E Barnetson, R StC Halliday, G M Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title | Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title_full | Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title_fullStr | Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title_full_unstemmed | Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title_short | Keratoacanthomas have an immunosuppressive cytokine environment of increased IL-10 and decreased GM-CSF compared to squamous cell carcinomas |
title_sort | keratoacanthomas have an immunosuppressive cytokine environment of increased il-10 and decreased gm-csf compared to squamous cell carcinomas |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363088/ https://www.ncbi.nlm.nih.gov/pubmed/10408389 http://dx.doi.org/10.1038/sj.bjc.6690552 |
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