Angiogenesis-related growth factors and cytokines in the serum of patients with B non-Hodgkin lymphoma; relation to clinical features and response to treatment

Summary Increased angiogenesis has been shown to be a feature of non‐Hodgkin lymphomas (NHL). In the current study, the pretreatment levels of circulating molecules related to angiogenesis were determined in 49 B‐cell NHL patients and correlated with histological grade, disease stage and prognostic...

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Published in:International journal of laboratory hematology Vol. 30; no. 1; pp. 17 - 25
Main Authors: PASSAM, F. H., SFIRIDAKI, A., PAPPA, C., KYRIAKOU, D., PETRELI, E., ROUSSOU, P. A., ALEXANDRAKIS, M. G.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-02-2008
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Summary:Summary Increased angiogenesis has been shown to be a feature of non‐Hodgkin lymphomas (NHL). In the current study, the pretreatment levels of circulating molecules related to angiogenesis were determined in 49 B‐cell NHL patients and correlated with histological grade, disease stage and prognostic score. In 25 patients, the same molecules were defined after standard treatment. Vascular endothelial growth factor (VEGF), angiogenin, interleukin‐2 (IL‐2), IL‐6, IL‐8 and IL‐16 were measured. Increased levels of VEGF, IL‐6 and IL‐8 were found in the whole group of untreated patients in comparison with normal controls (P < 0.05), whereas, IL‐2 was higher in the subgroup of indolent NHL. Overall, there was no significant decrease in the levels of these molecules after treatment. However, by stratification into group of responders vs. non‐responders pretreatment IL‐8 was significantly increased whereas IL‐16 was decreased in the subgroup of complete responders. According to the REAL classification IL‐2 was higher in the low risk compared with intermediate plus high‐risk group. There was no association with disease stage or the International Prognostic Score. Both indolent and aggressive B cell lymphomas have increased production of angiogenic mediators and cytokines with IL‐8 and IL‐16 potentially reflecting the response to treatment.
Bibliography:ark:/67375/WNG-3T6Q2BSF-7
istex:553C31E21804C5647B2187AC6B566585BEE93AA6
ArticleID:IJLH890
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1751-5521
1751-553X
DOI:10.1111/j.1365-2257.2006.00890.x