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Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs

BACKGROUND: Seminomas in the dog have traditionally been assumed to resemble human spermatocytic seminomas, based on their low malignancy and high occurrence in old individuals. However, recently published studies indicate that canine seminomas can be classified as classical and spermatocytic semino...

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Autores principales: Thorvaldsen, Tor Espen, Nødtvedt, Ane, Grotmol, Tom, Gunnes, Gjermund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515500/
https://www.ncbi.nlm.nih.gov/pubmed/22986090
http://dx.doi.org/10.1186/1751-0147-54-52
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author Thorvaldsen, Tor Espen
Nødtvedt, Ane
Grotmol, Tom
Gunnes, Gjermund
author_facet Thorvaldsen, Tor Espen
Nødtvedt, Ane
Grotmol, Tom
Gunnes, Gjermund
author_sort Thorvaldsen, Tor Espen
collection PubMed
description BACKGROUND: Seminomas in the dog have traditionally been assumed to resemble human spermatocytic seminomas, based on their low malignancy and high occurrence in old individuals. However, recently published studies indicate that canine seminomas can be classified as classical and spermatocytic seminomas in a similar way as in man, and that classical seminomas comprise a substantial proportion of seminomas in the dog. These two factors both contribute to increasing the potential of canine seminoma as a relevant model for human testicular cancer. The aim of the present study was to characterise seminoma in Norwegian dogs using morphology and immunohistochemistry, and determine whether these tumours are comparable with human classical seminoma. METHODS: By applying diagnostic criteria from human pathology, 45 seminomas from the Norwegian Canine Cancer Register were examined histologically with hematoxylin and eosin (HE) and periodic acid-Schiff (PAS) stains. All sections were stained immunohistochemically with antibodies against human placental alkaline phosphatase (PLAP) and the transmembrane receptor c-KIT. RESULTS: Although two of the seminomas showed immunohistochemical staining characteristics indicative of classical seminoma (PLAP+/c-KIT+), all 45 examined seminomas were morphologically consistent with spermatocytic seminoma. CONCLUSIONS: The value of canine seminoma as a model for SE in man remains unclear. Among the 45 investigated tumours from Norwegian dogs, none were classified as classical seminoma based on morphological criteria consistent with human seminomas. Regional or breed differences in the occurrence of classical seminoma in the dog, as well as the lack of uniform diagnostic criteria, might explain the discrepancy between the findings in the current study and the results presented by other authors.
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spelling pubmed-35155002012-12-06 Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs Thorvaldsen, Tor Espen Nødtvedt, Ane Grotmol, Tom Gunnes, Gjermund Acta Vet Scand Research BACKGROUND: Seminomas in the dog have traditionally been assumed to resemble human spermatocytic seminomas, based on their low malignancy and high occurrence in old individuals. However, recently published studies indicate that canine seminomas can be classified as classical and spermatocytic seminomas in a similar way as in man, and that classical seminomas comprise a substantial proportion of seminomas in the dog. These two factors both contribute to increasing the potential of canine seminoma as a relevant model for human testicular cancer. The aim of the present study was to characterise seminoma in Norwegian dogs using morphology and immunohistochemistry, and determine whether these tumours are comparable with human classical seminoma. METHODS: By applying diagnostic criteria from human pathology, 45 seminomas from the Norwegian Canine Cancer Register were examined histologically with hematoxylin and eosin (HE) and periodic acid-Schiff (PAS) stains. All sections were stained immunohistochemically with antibodies against human placental alkaline phosphatase (PLAP) and the transmembrane receptor c-KIT. RESULTS: Although two of the seminomas showed immunohistochemical staining characteristics indicative of classical seminoma (PLAP+/c-KIT+), all 45 examined seminomas were morphologically consistent with spermatocytic seminoma. CONCLUSIONS: The value of canine seminoma as a model for SE in man remains unclear. Among the 45 investigated tumours from Norwegian dogs, none were classified as classical seminoma based on morphological criteria consistent with human seminomas. Regional or breed differences in the occurrence of classical seminoma in the dog, as well as the lack of uniform diagnostic criteria, might explain the discrepancy between the findings in the current study and the results presented by other authors. BioMed Central 2012-09-17 /pmc/articles/PMC3515500/ /pubmed/22986090 http://dx.doi.org/10.1186/1751-0147-54-52 Text en Copyright ©2012 Thorvaldsen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Thorvaldsen, Tor Espen
Nødtvedt, Ane
Grotmol, Tom
Gunnes, Gjermund
Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title_full Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title_fullStr Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title_full_unstemmed Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title_short Morphological and immunohistochemical characterisation of seminomas in Norwegian dogs
title_sort morphological and immunohistochemical characterisation of seminomas in norwegian dogs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515500/
https://www.ncbi.nlm.nih.gov/pubmed/22986090
http://dx.doi.org/10.1186/1751-0147-54-52
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