Abstract
The aim of the study was to investigate the expression of angio- and lymphangiogenic molecules (vascular endothelial growth factors VEGF and VEGF-C and their receptors Flt-1, KDR, and Flt-4) in non-Hodgkin lymphomas (NHL) treated in the pre-rituximab era. Pre-therapeutic lymph-node biopsies from 155 patients with NHL (64 follicular lymphomas (FLs), 47 de novo diffuse large B-cell lymphomas (DLBCL) and 44 peripheral T-cell lymphomas (PTCL)) were stained by in situ hybridization and immunohistochemistry. Tumor cell expression of VEGF, VEGF-C and their receptors was detected in most of the analyzed biopsies. In FL, diffuse intratumoral VEGF staining correlated with shorter overall survival (OS) (p = 0.008) and diffuse KDR staining was associated with a higher risk of histologic transformation (p = 0.05). In DLBCL, high KDR expression predicted poor treatment response (p = 0.03) and had a significant adverse impact on OS (p < 0.001). In PTCL, diffuse tissue distribution of VEGF mRNA correlated with an unfavorable 5-year OS (p = 0.004).
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Cell Nucleus / chemistry
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Cytoplasm / chemistry
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Female
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Gene Expression Profiling
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Humans
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Lymph Nodes / chemistry
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Lymph Nodes / pathology
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Lymphoma, Follicular / genetics*
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Lymphoma, Follicular / mortality
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Lymphoma, Follicular / pathology
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Lymphoma, Large B-Cell, Diffuse / genetics*
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Lymphoma, Large B-Cell, Diffuse / mortality
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Lymphoma, Large B-Cell, Diffuse / pathology
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Lymphoma, T-Cell, Peripheral / genetics*
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Lymphoma, T-Cell, Peripheral / mortality
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Lymphoma, T-Cell, Peripheral / pathology
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Male
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Middle Aged
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Neoplasm Proteins / analysis*
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Neoplasm Proteins / biosynthesis
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Neoplasm Proteins / genetics
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Neovascularization, Pathologic / etiology
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Neovascularization, Pathologic / genetics
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Prognosis
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RNA, Messenger / analysis
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RNA, Messenger / biosynthesis
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RNA, Messenger / genetics
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RNA, Neoplasm / analysis
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RNA, Neoplasm / biosynthesis
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RNA, Neoplasm / genetics
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Retrospective Studies
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Vascular Endothelial Growth Factor A / analysis*
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Vascular Endothelial Growth Factor A / biosynthesis
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Vascular Endothelial Growth Factor A / genetics
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Vascular Endothelial Growth Factor C / analysis*
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Vascular Endothelial Growth Factor C / biosynthesis
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Vascular Endothelial Growth Factor C / genetics
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Vascular Endothelial Growth Factor Receptor-1 / analysis*
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Vascular Endothelial Growth Factor Receptor-1 / biosynthesis
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Vascular Endothelial Growth Factor Receptor-1 / genetics
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Vascular Endothelial Growth Factor Receptor-2 / analysis*
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Vascular Endothelial Growth Factor Receptor-2 / biosynthesis
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Vascular Endothelial Growth Factor Receptor-2 / genetics
Substances
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Neoplasm Proteins
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RNA, Messenger
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RNA, Neoplasm
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VEGFA protein, human
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VEGFC protein, human
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Vascular Endothelial Growth Factor A
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Vascular Endothelial Growth Factor C
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Vascular Endothelial Growth Factor Receptor-1
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Vascular Endothelial Growth Factor Receptor-2