Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells

Cooperation between endothelial cells and bone in bone remodelling is well established. In contrast, bone microvasculature supporting the growth of primary tumors and metastasis is poorly understood. Several antiangiogenic agents have recently been undergoing trials, although an extensive body of cl...

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Main Authors: Gaetano Apice, Cristina Tutucci, Annarosaria De Chiara, Flavio Fazioli, Michele Gallo, Elena Cesario, Teresa Infante, Filomena de Nigris
Format: Article
Language:English
Published: MDPI AG 2013-04-01
Series:Cancers
Subjects:
Online Access:http://www.mdpi.com/2072-6694/5/2/404
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spelling doaj-e1e2138984094a2880f1ae32309354ea2020-11-24T23:54:07ZengMDPI AGCancers2072-66942013-04-015240441710.3390/cancers5020404Ex Vivo Behaviour of Human Bone Tumor Endothelial CellsGaetano ApiceCristina TutucciAnnarosaria De ChiaraFlavio FazioliMichele GalloElena CesarioTeresa InfanteFilomena de NigrisCooperation between endothelial cells and bone in bone remodelling is well established. In contrast, bone microvasculature supporting the growth of primary tumors and metastasis is poorly understood. Several antiangiogenic agents have recently been undergoing trials, although an extensive body of clinical data and experimental research have proved that angiogenic pathways differ in each tumor type and stage. Here, for the first time, we characterize at the molecular and functional level tumor endothelial cells from human bone sarcomas at different stages of disease and with different histotypes. We selected a CD31+ subpopulation from biopsies that displayed the capability to grow as adherent cell lines without vascular endothelial growth factor (VEGF). Our findings show the existence in human primary bone sarcomas of highly proliferative endothelial cells expressing CD31, CD44, CD105, CD146 and CD90 markers. These cells are committed to develop capillary-like structures and colony formation units, and to produce nitric oxide. We believe that a better understanding of tumor vasculature could be a valid tool for the design of an efficacious antiangiogenic therapy as adjuvant treatment of sarcomas.http://www.mdpi.com/2072-6694/5/2/404sarcomasangiogenesisendothelial cellstumor microenvironment
collection DOAJ
language English
format Article
sources DOAJ
author Gaetano Apice
Cristina Tutucci
Annarosaria De Chiara
Flavio Fazioli
Michele Gallo
Elena Cesario
Teresa Infante
Filomena de Nigris
spellingShingle Gaetano Apice
Cristina Tutucci
Annarosaria De Chiara
Flavio Fazioli
Michele Gallo
Elena Cesario
Teresa Infante
Filomena de Nigris
Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
Cancers
sarcomas
angiogenesis
endothelial cells
tumor microenvironment
author_facet Gaetano Apice
Cristina Tutucci
Annarosaria De Chiara
Flavio Fazioli
Michele Gallo
Elena Cesario
Teresa Infante
Filomena de Nigris
author_sort Gaetano Apice
title Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
title_short Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
title_full Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
title_fullStr Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
title_full_unstemmed Ex Vivo Behaviour of Human Bone Tumor Endothelial Cells
title_sort ex vivo behaviour of human bone tumor endothelial cells
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2013-04-01
description Cooperation between endothelial cells and bone in bone remodelling is well established. In contrast, bone microvasculature supporting the growth of primary tumors and metastasis is poorly understood. Several antiangiogenic agents have recently been undergoing trials, although an extensive body of clinical data and experimental research have proved that angiogenic pathways differ in each tumor type and stage. Here, for the first time, we characterize at the molecular and functional level tumor endothelial cells from human bone sarcomas at different stages of disease and with different histotypes. We selected a CD31+ subpopulation from biopsies that displayed the capability to grow as adherent cell lines without vascular endothelial growth factor (VEGF). Our findings show the existence in human primary bone sarcomas of highly proliferative endothelial cells expressing CD31, CD44, CD105, CD146 and CD90 markers. These cells are committed to develop capillary-like structures and colony formation units, and to produce nitric oxide. We believe that a better understanding of tumor vasculature could be a valid tool for the design of an efficacious antiangiogenic therapy as adjuvant treatment of sarcomas.
topic sarcomas
angiogenesis
endothelial cells
tumor microenvironment
url http://www.mdpi.com/2072-6694/5/2/404
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