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Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma
Background: Kaposi’s sarcoma (KS) is a rare neoplasm of lymphatic endothelial cells. Human herpes virus 8 (HHV-8) is considered to be a necessary, but not sufficient causal agent of KS and additional cofactors remain unknown. In this study we evaluated the expression of human β defensin (HBD)-3 and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782342/ https://www.ncbi.nlm.nih.gov/pubmed/24358820 http://dx.doi.org/10.12688/f1000research.1-38.v2 |
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author | Fathy, Hanan Amin, Maha M El-Gilany, Abdel-Hady |
author_facet | Fathy, Hanan Amin, Maha M El-Gilany, Abdel-Hady |
author_sort | Fathy, Hanan |
collection | PubMed |
description | Background: Kaposi’s sarcoma (KS) is a rare neoplasm of lymphatic endothelial cells. Human herpes virus 8 (HHV-8) is considered to be a necessary, but not sufficient causal agent of KS and additional cofactors remain unknown. In this study we evaluated the expression of human β defensin (HBD)-3 and LL-37 in cutaneous lesions of KS in comparison to the healthy skin of normal subjects. Methods: We performed a quantitative immunohistochemical study of HBD-3 and LL-37 on skin lesions from 18 patients having KS, and on healthy skin from 12 normal controls. Results: HBD-3 and LL-37 were significantly upregulated in epidermal and dermal specimens of all KS patients in comparison to normal skin of healthy controls. The immunostaining score of dermal HBD-3 was significantly higher in nodular lesions (9.6 ± 2.4) versus plaque lesions (4.1 ± 2.2), P = 0.001. Also the immunostaining score of dermal LL-37 was significantly higher in nodular lesions versus plaque lesions (P = 0.001). Conclusions: We have demonstrated for the first time that HBD-3 and LL-37 are significantly upregulated in lesional skin of KS in comparison to the skin of healthy controls. The obtained data suggest a possible involvement of these antimicrobial peptides in the pathogenesis of KS. However, the biological significance of HBD-3 and LL-37 in KS lesions needs further research. |
format | Online Article Text |
id | pubmed-3782342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-37823422013-12-05 Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma Fathy, Hanan Amin, Maha M El-Gilany, Abdel-Hady F1000Res Research Article Background: Kaposi’s sarcoma (KS) is a rare neoplasm of lymphatic endothelial cells. Human herpes virus 8 (HHV-8) is considered to be a necessary, but not sufficient causal agent of KS and additional cofactors remain unknown. In this study we evaluated the expression of human β defensin (HBD)-3 and LL-37 in cutaneous lesions of KS in comparison to the healthy skin of normal subjects. Methods: We performed a quantitative immunohistochemical study of HBD-3 and LL-37 on skin lesions from 18 patients having KS, and on healthy skin from 12 normal controls. Results: HBD-3 and LL-37 were significantly upregulated in epidermal and dermal specimens of all KS patients in comparison to normal skin of healthy controls. The immunostaining score of dermal HBD-3 was significantly higher in nodular lesions (9.6 ± 2.4) versus plaque lesions (4.1 ± 2.2), P = 0.001. Also the immunostaining score of dermal LL-37 was significantly higher in nodular lesions versus plaque lesions (P = 0.001). Conclusions: We have demonstrated for the first time that HBD-3 and LL-37 are significantly upregulated in lesional skin of KS in comparison to the skin of healthy controls. The obtained data suggest a possible involvement of these antimicrobial peptides in the pathogenesis of KS. However, the biological significance of HBD-3 and LL-37 in KS lesions needs further research. F1000Research 2012-12-14 /pmc/articles/PMC3782342/ /pubmed/24358820 http://dx.doi.org/10.12688/f1000research.1-38.v2 Text en Copyright: © 2012 Fathy H et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Research Article Fathy, Hanan Amin, Maha M El-Gilany, Abdel-Hady Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title | Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title_full | Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title_fullStr | Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title_full_unstemmed | Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title_short | Upregulation of human β-defensin-3 and cathelicidin LL-37 in Kaposi’s sarcoma |
title_sort | upregulation of human β-defensin-3 and cathelicidin ll-37 in kaposi’s sarcoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782342/ https://www.ncbi.nlm.nih.gov/pubmed/24358820 http://dx.doi.org/10.12688/f1000research.1-38.v2 |
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