Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5363
Title: VEGF-D is expressed in activated lymphoid cells and in tumors of hematopoietic and lymphoid tissues.
Authors: Bardelli, Monia
Leucci, Eleonora
Schürfeld, Karin
Bellan, Cristiana
Passiatore, Giovanni
Rocchigiani, Marina
Bartolommei, Sabrina
Orlandini, Maurizio 
Zagursky, Jennifer
Lazzi, Stefano
De Falco, Giulia
Tosi, Piero
Oliviero, Salvatore 
Leoncini, Lorenzo
Keywords: Angiogenesis; Leukemia; Lymphoma; VEGF-D; VEGFR-3; Antibodies, Monoclonal; Biopsy; Bone Marrow Cells; Cell Line, Tumor; HL-60 Cells; Hematopoietic Stem Cells; Humans; K562 Cells; Lymph Nodes; Lymphocytes; Vascular Endothelial Growth Factor D; Vascular Endothelial Growth Factor Receptor-2; Vascular Endothelial Growth Factor Receptor-3; Gene Expression Regulation, Leukemic; Gene Expression Regulation, Neoplastic; Cancer Research; Hematology; Oncology
Issue Date: 2007
Project: None 
Journal: LEUKEMIA & LYMPHOMA
Abstract: 
Vascular Endothelial Growth Factor (VEGF)-D is a member of the VEGF family of angiogenic growth factors that activate the Vascular Endothelial Growth Factor Receptor (VEGFR)-2 and VEGFR-3, which are mainly expressed in blood and lymphatic vessels. Here we have analyzed by using monoclonal antibodies, the expression of VEGF-D and its cognate receptor VEGFR-3 in normal and pathologic bone marrow and lymph node biopsies. This analysis revealed that VEGF-D is expressed in B cells of the germinal centers, scattered B and T blasts, myeloid progenitors, acute leukemia, several types of non Hodgkin lymphoma, and classical Hodgkin's lymphoma. In normal tissues VEGFR-3 was only expressed in fenestrated capillaries of bone marrow and in lymphatic vessels of lymph nodes, while in VEGF-D expressing tumors newly formed vessels, but not malignant cells, showed high VEGFR-3 expression. These data suggest that VEGF-D could contribute to leukemia and lymphoma growth via the induction of angiogenesis in bone marrow and lymphoid tissues.
Description: 
36552
URI: http://hdl.handle.net/20.500.12779/5363
ISSN: 1042-8194
DOI: 10.1080/10428190701540975
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