Detailed Information on Publication Record
2018
The Plasma Levels of the Angiogenic Cytokine Endocan Are Elevated in Patients with Multiple Myeloma
STEINER, Normann, Roman HAJEK, Sabina ŠEVČÍKOVÁ, Bojana BORJAN, Gerold UNTERGASSER et. al.Basic information
Original name
The Plasma Levels of the Angiogenic Cytokine Endocan Are Elevated in Patients with Multiple Myeloma
Authors
STEINER, Normann (40 Austria, guarantor), Roman HAJEK (203 Czech Republic), Sabina ŠEVČÍKOVÁ (203 Czech Republic, belonging to the institution), Bojana BORJAN (40 Austria), Gerold UNTERGASSER (40 Austria), Georg GOBEL (40 Austria) and Eberhard GUNSILIUS (40 Austria)
Edition
Anticancer Research, Athens, International Institute of Anticancer Research, 2018, 0250-7005
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Greece
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 1.935
RIV identification code
RIV/00216224:14110/18:00105233
Organization unit
Faculty of Medicine
UT WoS
000449957600014
Keywords in English
Multiple myeloma; endocan; biomarker
Tags
International impact, Reviewed
Změněno: 11/2/2019 14:16, Soňa Böhmová
Abstract
V originále
Background/Aim: Monoclonal gammopathy of unknown significance (MGUS) and smoldering multiple myeloma often precede multiple myeloma (MM). The identification of biomarkers predicting progression to MM might facilitate an earlier diagnosis of MM. Our study assessed the diagnostic value of plasma levels of endocan, a 50-kDa soluble dermatan sulfate proteoglycan produced and secreted by endothelial cells, hitherto unknown in MM, in patients with plasma cell dyscrasia. Materials and Methods: Endocan levels were determined in 96 peripheral blood plasma samples by sandwich enzyme-linked immunosorbent assay (ELISA) in healthy controls (n=12), in patients with MGUS (n=17), and in patients newly diagnosed with (n=42) or relapsed/refractory (n=25) MM. Results: Median endocan concentration increased from MGUS (315.00 pg/ml) and healthy controls (316.19 pg/ml) to newly-diagnosed MM (371.82 pg/ml; p=0.027). The low endocan levels (median=246 .20 pg/ml) in patients with relapsed/refractory MM were similar to those in healthy controls and patients with MG US. A cut-off value of >220 pg/ml endocan in peripheral blood discriminated patients newly diagnosed with MM from those with MGUS (area under the curve(AUC)=0.66, 95% confidence interval(CI)=0.55-0.81). Conclusion: The plasma levels of endocan can non-invasively differentiate patients newly diagnosed with MM from those with MGUS and should therefore be evaluated prospectively as a potential diagnostic marker.