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Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations
INTRODUCTION: Chronic venous disease (CVD) is a disabling condition affecting about 1% to 3% of the general population. Besides varicose veins, CVD can result also in the formation of severe skin lesions, especially venous ulcerations (VU). The exact mechanism of VU is still unknown. AIM: To evaluat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262799/ https://www.ncbi.nlm.nih.gov/pubmed/32489360 http://dx.doi.org/10.5114/ada.2020.94840 |
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author | Kolano, Paweł Bednarski, Igor A. Lesiak, Aleksandra Skibińska, Małgorzata Stasikowska-Kanicka, Olga Danilewicz, Marian Narbutt, Joanna |
author_facet | Kolano, Paweł Bednarski, Igor A. Lesiak, Aleksandra Skibińska, Małgorzata Stasikowska-Kanicka, Olga Danilewicz, Marian Narbutt, Joanna |
author_sort | Kolano, Paweł |
collection | PubMed |
description | INTRODUCTION: Chronic venous disease (CVD) is a disabling condition affecting about 1% to 3% of the general population. Besides varicose veins, CVD can result also in the formation of severe skin lesions, especially venous ulcerations (VU). The exact mechanism of VU is still unknown. AIM: To evaluate immunoexpression of vascular endothelial growth factor (VEGF) and cathepsin K in healthy individuals and patients with VU. MATERIAL AND METHODS: The study included 12 patients with venous ulcers and 10 healthy individuals who served as controls; both groups were sex- and age-matched. Biopsy samples were obtained from lower leg areas and submitted to histochemical analysis. RESULTS: There was a significant difference between the study group and the control group in cathepsin K expression (1.007 ±0.3 vs. 0.22 ±0.2, respectively, p < 0.001) and VEGF expression (1.17 ±0.59 vs. 0.27 ±0.19, respectively, p < 0.001). Additionally, the microvessel density (per mm(2)) differed significantly between the study group and the control group (97.6 ±28.81 vs. 59.32 ±12.71, respectively, p < 0.001). We found no correlation between cathepsin K and microvessel density, and cathepsin K and VEGF in both groups, but there was a significant correlation between microvessel density and VEGF immunoexpression in the study group (r = 0.82, p = 0.002). CONCLUSIONS: Increased immunoexpression of VEGF and cathepsin K suggests that both of these proteins may play a role in VU development. |
format | Online Article Text |
id | pubmed-7262799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-72627992020-06-01 Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations Kolano, Paweł Bednarski, Igor A. Lesiak, Aleksandra Skibińska, Małgorzata Stasikowska-Kanicka, Olga Danilewicz, Marian Narbutt, Joanna Postepy Dermatol Alergol Original Paper INTRODUCTION: Chronic venous disease (CVD) is a disabling condition affecting about 1% to 3% of the general population. Besides varicose veins, CVD can result also in the formation of severe skin lesions, especially venous ulcerations (VU). The exact mechanism of VU is still unknown. AIM: To evaluate immunoexpression of vascular endothelial growth factor (VEGF) and cathepsin K in healthy individuals and patients with VU. MATERIAL AND METHODS: The study included 12 patients with venous ulcers and 10 healthy individuals who served as controls; both groups were sex- and age-matched. Biopsy samples were obtained from lower leg areas and submitted to histochemical analysis. RESULTS: There was a significant difference between the study group and the control group in cathepsin K expression (1.007 ±0.3 vs. 0.22 ±0.2, respectively, p < 0.001) and VEGF expression (1.17 ±0.59 vs. 0.27 ±0.19, respectively, p < 0.001). Additionally, the microvessel density (per mm(2)) differed significantly between the study group and the control group (97.6 ±28.81 vs. 59.32 ±12.71, respectively, p < 0.001). We found no correlation between cathepsin K and microvessel density, and cathepsin K and VEGF in both groups, but there was a significant correlation between microvessel density and VEGF immunoexpression in the study group (r = 0.82, p = 0.002). CONCLUSIONS: Increased immunoexpression of VEGF and cathepsin K suggests that both of these proteins may play a role in VU development. Termedia Publishing House 2020-05-06 2020-04 /pmc/articles/PMC7262799/ /pubmed/32489360 http://dx.doi.org/10.5114/ada.2020.94840 Text en Copyright: © 2020 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Kolano, Paweł Bednarski, Igor A. Lesiak, Aleksandra Skibińska, Małgorzata Stasikowska-Kanicka, Olga Danilewicz, Marian Narbutt, Joanna Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title | Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title_full | Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title_fullStr | Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title_full_unstemmed | Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title_short | Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations |
title_sort | overexpression of cathepsin k and vascular endothelial growth factor in chronic venous ulcerations |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262799/ https://www.ncbi.nlm.nih.gov/pubmed/32489360 http://dx.doi.org/10.5114/ada.2020.94840 |
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