Angiogenesis-Related Cytokines, RANKL, and Osteoprotegerin in Multiple Myeloma Patients in relation to Clinical Features and Response to Treatment

被引:17
|
作者
Sfiridaki, K.
Pappa, C. A.
Tsirakis, G. [1 ,2 ]
Kanellou, P. [1 ,2 ]
Kaparou, M. [1 ,2 ]
Stratinaki, M.
Sakellaris, G. [3 ]
Kontakis, G. [3 ]
Alexandrakis, M. G. [1 ]
机构
[1] Univ Hosp Herakl, Dept Haematol, Iraklion 70013, Greece
[2] Venizel Gen Hosp Herakl, Blood Bank, Iraklion 71409, Greece
[3] Univ Hosp Herakl, Dept Surg, Iraklion 70013, Greece
关键词
ENDOTHELIAL GROWTH-FACTOR; SERUM-LEVELS; OSTEOCLAST DIFFERENTIATION; BIOCHEMICAL MARKERS; SCATTER FACTOR; BONE-DISEASE; FACTOR VEGF; RECEPTOR; LIGAND; NEOVASCULARIZATION;
D O I
10.1155/2011/867576
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An essential cytokine system for the osteoclast biology in multiple myeloma (MM) consists of the receptor of activator of NF-kappa B ligand (RANKL), its receptor (RANK), and the soluble decoy receptor, osteoprotegerin (OPG). Myeloma cells cause imbalance in OPG/RANKL interactions. We measured serum levels of OPG, soluble (s) RANKL, sRANKL/OPG ratio, markers of disease activity [LDH, CRP, interleukin-6 (IL-6), beta 2-microglobulin (B2M)], and angiogenic factors [hepatocyte growth factor (HGF), vascular endothelial growth factor (VEGF)], in 54 newly diagnosedMMpatients and in 25 of them in plateau phase. All the above values were higher in MM patients compared to controls and decreased in plateau phase. sRANKL and RANKL/OPG were higher with advancing disease stage and skeletal grade. Significant correlations were found among RANKL and RANKL/OPG with HGF, LDH, VEGF, IL-6, and B2M. In conclusion, RANKL and OPG play significant roles in MM pathophysiology, as regulators of bone turnover and mediators of angiogenesis.
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页数:7
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