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VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model

Canine cutaneous mast cell tumour (CMCT) is a common cutaneous tumour in dog, with a higher incidence than in human. CMCT is classified in three subgroups, well and intermediately differentiated (G1 and G2), corresponding to a benign disease, and poorly differentiated (G3), corresponding to a malign...

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Autores principales: Patruno, R, Arpaia, N, Gadaleta, CD, Passantino, L, Zizzo, N, Misino, A, Lucarelli, NM, Catino, A, Valerio, P, Ribatti, D, Ranieri, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822515/
https://www.ncbi.nlm.nih.gov/pubmed/18429933
http://dx.doi.org/10.1111/j.1582-4934.2008.00355.x
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author Patruno, R
Arpaia, N
Gadaleta, CD
Passantino, L
Zizzo, N
Misino, A
Lucarelli, NM
Catino, A
Valerio, P
Ribatti, D
Ranieri, G
author_facet Patruno, R
Arpaia, N
Gadaleta, CD
Passantino, L
Zizzo, N
Misino, A
Lucarelli, NM
Catino, A
Valerio, P
Ribatti, D
Ranieri, G
author_sort Patruno, R
collection PubMed
description Canine cutaneous mast cell tumour (CMCT) is a common cutaneous tumour in dog, with a higher incidence than in human. CMCT is classified in three subgroups, well and intermediately differentiated (G1 and G2), corresponding to a benign disease, and poorly differentiated (G3), corresponding to a malignant disease, which metastasize to lymph nodes, liver, spleen and bone marrow. In this study, we have evaluated serum (S), platelet-poor plasma (P-PP), plasma-activated platelet rich (P-APR) and cytosol vascular endothelial growth factor (VEGF) concentrations, microvascular density (MVD) and mast cell density (MCD) in a series of 86 CMCTs and we have correlated these parameters with each other, by means of ELISA detection of VEGF and immunohistochemistry. Results show that VEGF level from cytosol P-APR and MVD were significantly higher in G3 CMCTs as compared to G1 or G2 subgroups. Moreover, a significantly strong correlation among VEGF levels from P-PAR and cytosol, MVD and MCD was found in G3 subgroup. Because VEGF levels from P-APR well correlated with MVD and malignancy grade in CMCT, we suggest that VEGF might be secreted from MCs and it may be a suitable surrogate inter-species angiogenetic markers of tumour progression in CMCT. Finally, CMCT seems to be a useful model to study the role of MCs in tumour angiogenesis and inhibition of MCs degranulation or activation might be a new anti-angiogenic strategy worthy to further investigations.
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spelling pubmed-38225152015-04-27 VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model Patruno, R Arpaia, N Gadaleta, CD Passantino, L Zizzo, N Misino, A Lucarelli, NM Catino, A Valerio, P Ribatti, D Ranieri, G J Cell Mol Med Articles Canine cutaneous mast cell tumour (CMCT) is a common cutaneous tumour in dog, with a higher incidence than in human. CMCT is classified in three subgroups, well and intermediately differentiated (G1 and G2), corresponding to a benign disease, and poorly differentiated (G3), corresponding to a malignant disease, which metastasize to lymph nodes, liver, spleen and bone marrow. In this study, we have evaluated serum (S), platelet-poor plasma (P-PP), plasma-activated platelet rich (P-APR) and cytosol vascular endothelial growth factor (VEGF) concentrations, microvascular density (MVD) and mast cell density (MCD) in a series of 86 CMCTs and we have correlated these parameters with each other, by means of ELISA detection of VEGF and immunohistochemistry. Results show that VEGF level from cytosol P-APR and MVD were significantly higher in G3 CMCTs as compared to G1 or G2 subgroups. Moreover, a significantly strong correlation among VEGF levels from P-PAR and cytosol, MVD and MCD was found in G3 subgroup. Because VEGF levels from P-APR well correlated with MVD and malignancy grade in CMCT, we suggest that VEGF might be secreted from MCs and it may be a suitable surrogate inter-species angiogenetic markers of tumour progression in CMCT. Finally, CMCT seems to be a useful model to study the role of MCs in tumour angiogenesis and inhibition of MCs degranulation or activation might be a new anti-angiogenic strategy worthy to further investigations. Blackwell Publishing Ltd 2009-03 2008-04-18 /pmc/articles/PMC3822515/ /pubmed/18429933 http://dx.doi.org/10.1111/j.1582-4934.2008.00355.x Text en © 2009 The Authors Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Patruno, R
Arpaia, N
Gadaleta, CD
Passantino, L
Zizzo, N
Misino, A
Lucarelli, NM
Catino, A
Valerio, P
Ribatti, D
Ranieri, G
VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title_full VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title_fullStr VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title_full_unstemmed VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title_short VEGF concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
title_sort vegf concentration from plasma-activated platelets rich correlates with microvascular density and grading in canine mast cell tumour spontaneous model
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822515/
https://www.ncbi.nlm.nih.gov/pubmed/18429933
http://dx.doi.org/10.1111/j.1582-4934.2008.00355.x
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