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Cellular atypia is negatively correlated with immunohistochemical reactivity of CD31 and vWF expression levels in canine hemangiosarcoma
Canine hemangiosarcoma (HSA) is one of the most common mesenchymal tumors in dogs. Its high metastatic and growth rates are usually associated with poor prognosis. Neoplastic cells of HSA can show various levels of cellular atypia in the same mass and may consist of various populations at different...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836755/ https://www.ncbi.nlm.nih.gov/pubmed/29311493 http://dx.doi.org/10.1292/jvms.17-0561 |
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author | MAHARANI, Aprilia AOSHIMA, Keisuke ONISHI, Shinichi GULAY, Kevin Christian Montecillo KOBAYASHI, Atsushi KIMURA, Takashi |
author_facet | MAHARANI, Aprilia AOSHIMA, Keisuke ONISHI, Shinichi GULAY, Kevin Christian Montecillo KOBAYASHI, Atsushi KIMURA, Takashi |
author_sort | MAHARANI, Aprilia |
collection | PubMed |
description | Canine hemangiosarcoma (HSA) is one of the most common mesenchymal tumors in dogs. Its high metastatic and growth rates are usually associated with poor prognosis. Neoplastic cells of HSA can show various levels of cellular atypia in the same mass and may consist of various populations at different differentiated stages. Up to present, however, there is no report analyzing their differentiation states by comparing cellular atypia with differentiation-related protein expressions. To evaluate whether cellular atypia can be used as a differentiation marker in HSA, we analyzed correlation between cellular atypia and intensities of CD31 and von Willebrand Factor (vWF) staining in HSA cases. We also compared cellular atypia and expression levels of CD31 and vWF in each growth patterns. Our results show that cellular atypia was negatively correlated to CD31 and vWF expression levels but no significant correlation was found between growth patterns and cellular atypia or CD31 and vWF expression levels. Our study suggests that cellular atypia is useful for identifying differentiation levels in HSA cases. This study also provides useful information to determine differentiation levels of cell populations within HSA based only on morphological analysis, which will aid further HSA research such as identifying undifferentiation markers of endothelial cells or finding undifferentiated cell population in tissue sections. |
format | Online Article Text |
id | pubmed-5836755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58367552018-03-09 Cellular atypia is negatively correlated with immunohistochemical reactivity of CD31 and vWF expression levels in canine hemangiosarcoma MAHARANI, Aprilia AOSHIMA, Keisuke ONISHI, Shinichi GULAY, Kevin Christian Montecillo KOBAYASHI, Atsushi KIMURA, Takashi J Vet Med Sci Pathology Canine hemangiosarcoma (HSA) is one of the most common mesenchymal tumors in dogs. Its high metastatic and growth rates are usually associated with poor prognosis. Neoplastic cells of HSA can show various levels of cellular atypia in the same mass and may consist of various populations at different differentiated stages. Up to present, however, there is no report analyzing their differentiation states by comparing cellular atypia with differentiation-related protein expressions. To evaluate whether cellular atypia can be used as a differentiation marker in HSA, we analyzed correlation between cellular atypia and intensities of CD31 and von Willebrand Factor (vWF) staining in HSA cases. We also compared cellular atypia and expression levels of CD31 and vWF in each growth patterns. Our results show that cellular atypia was negatively correlated to CD31 and vWF expression levels but no significant correlation was found between growth patterns and cellular atypia or CD31 and vWF expression levels. Our study suggests that cellular atypia is useful for identifying differentiation levels in HSA cases. This study also provides useful information to determine differentiation levels of cell populations within HSA based only on morphological analysis, which will aid further HSA research such as identifying undifferentiation markers of endothelial cells or finding undifferentiated cell population in tissue sections. The Japanese Society of Veterinary Science 2018-01-01 2018-02 /pmc/articles/PMC5836755/ /pubmed/29311493 http://dx.doi.org/10.1292/jvms.17-0561 Text en ©2018 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Pathology MAHARANI, Aprilia AOSHIMA, Keisuke ONISHI, Shinichi GULAY, Kevin Christian Montecillo KOBAYASHI, Atsushi KIMURA, Takashi Cellular atypia is negatively correlated with immunohistochemical reactivity of CD31 and vWF expression levels in canine hemangiosarcoma |
title | Cellular atypia is negatively correlated with immunohistochemical reactivity
of CD31 and vWF expression levels in canine hemangiosarcoma |
title_full | Cellular atypia is negatively correlated with immunohistochemical reactivity
of CD31 and vWF expression levels in canine hemangiosarcoma |
title_fullStr | Cellular atypia is negatively correlated with immunohistochemical reactivity
of CD31 and vWF expression levels in canine hemangiosarcoma |
title_full_unstemmed | Cellular atypia is negatively correlated with immunohistochemical reactivity
of CD31 and vWF expression levels in canine hemangiosarcoma |
title_short | Cellular atypia is negatively correlated with immunohistochemical reactivity
of CD31 and vWF expression levels in canine hemangiosarcoma |
title_sort | cellular atypia is negatively correlated with immunohistochemical reactivity
of cd31 and vwf expression levels in canine hemangiosarcoma |
topic | Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836755/ https://www.ncbi.nlm.nih.gov/pubmed/29311493 http://dx.doi.org/10.1292/jvms.17-0561 |
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