Detailed Information on Publication Record
2005
Plasma concentrations of vascular endothelial growth factor and basic fibroblast growth factor in lymphoproliferative disorders.
SMOLEJ, L., C. ANDRÝS, Vladimír MAISNAR, Luděk POUR, J. MALÝ et. al.Basic information
Original name
Plasma concentrations of vascular endothelial growth factor and basic fibroblast growth factor in lymphoproliferative disorders.
Name in Czech
Hladiny endoteliálního růstového faktoru a fibroblastového růstového faktoru v plazmě u lymfoproliferativních onemocnění
Authors
SMOLEJ, L. (203 Czech Republic), C. ANDRÝS (203 Czech Republic), Vladimír MAISNAR (203 Czech Republic), Luděk POUR (203 Czech Republic, guarantor) and J. MALÝ (203 Czech Republic)
Edition
Acta medica (Hradec Králové), Hradec Králové, Czech Republic, Facultas Medica, Universitas Carolina, 2005, 1211-4286
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
RIV identification code
RIV/00216224:14110/05:00035961
Organization unit
Faculty of Medicine
Keywords (in Czech)
angiogeneze; VEGF; bFGF;
Keywords in English
Angiogenesis; VEGF; bFGF; Leukemia; Lymphoma; Myeloma
Tags
Reviewed
Změněno: 24/6/2009 11:33, Mgr. Anna Potáčová, Ph.D.
V originále
Angiogenesis plays a major role in the development and progression of haematological malignancies. In our study we measured plasma concentrations of key angiogenic activators vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) using comercially available sandwich enzyme-linked immunosorbent assay (ELISA) in 37 patients with lymphoid malignancies and 20 healthy donors. We found a statistically significant increase in bFGF concentrations in patients with B-cell chronic lymphocytic leukemia (B-CLL, n=18) compared to the control group (median 118.8 vs. 9.3 pg/ml, p<0.001). However, we didn't find any significant difference in VEGF concentrations between B-CLL patients and the control group. There was also no significant increase in bFGF or VEGF in patients with multiple myeloma (n=7) and non-Hodgkin's lymphoma (n=12). Our pilot study shows that measurement of angiogenic activators in plasma is a feasible and reproducible method of angiogenesis assessment. Larger studies are needed for correlation between serum and plasma concentrations and detailed statistical evaluation including the impact on patients' survival.
In Czech
Publikace shnuje výsledky měření koncentrací plazmatických hladin VEGF a bFGF u pacientů s lymfoproliferativními onemocněními.