Serum proinflammatory mediators at different periods of therapy in patients with multiple myeloma

被引:29
作者
Kuku, I [1 ]
Bayraktar, MR
Kaya, E
Erkurt, MA
Bayraktar, N
Cikim, K
Aydogdu, I
机构
[1] Inonu Univ, Fac Med, Dept Hematol, Turgut Ozal Med Ctr, TR-44069 Malatya, Turkey
[2] Inonu Univ, Fac Med, Dept Med Microbiol, Turgut Ozal Med Ctr, TR-44069 Malatya, Turkey
[3] Inonu Univ, Fac Med, Dept Clin Biochem, Turgut Ozal Med Ctr, TR-44069 Malatya, Turkey
关键词
D O I
10.1155/MI.2005.171
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multiple myeloma (MM) is a malignant disease characterized by the clonal proliferation of plasma cells within the bone marrow. Several cytokines have been demonstrated to be involved in the control of growth, progression, and dissemination of MM. We determined serum levels of interleukin-1 beta (IL- 1 beta), Soluble interleukin-2 receptor (sIL-2R), interleukin-6 (IL-6), interleukin-8 (IL-8), tumor necrosis factor-alpha (TNF-alpha), and C-reactive protein (CRP) in 14 newly diagnosed MM patients. The median age of the patients was 63.4 +/- 10.8 years and all of the patients were stage III (classified according to the Durie-Salmon classification). The same parameters were measured in 15 healthy controls. In addition, we also examined the effects of vincristine-adriamycin-dexamethasone (VAD) therapy on the same parameters and mediators as well as the relationship among the parameters in the same patient groups. The serum concentrations of TNF-alpha, IL-1 beta, sIL-2R, I L-6, IL-8, and CRP (18.6 +/- 3.7 pg/mL, 10.1 +/- 2.8 pg/mL, 730 +/- 220 U/mL, 11.4 +/- 3.3 pg/mL, 23.9 +/- 8.3 pg/mL, and 49.9 +/- 19.5 mg/dL, resp) were significantly higher in newly diagnosed MM patients than ill healthy controls (P <.0001). All of the parameters were found to be significantly reduced after chemotherapy. In conclusion, we found that after the VAD therapy, the level of these cytokines which are thought to play an important role in the pathogenesis of MM was significantly suppressed. This is the first study demonstrating strong impact of VAD treatment on circulating mediators of sIL-2R and IL-8 levels parameters.
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页码:171 / 174
页数:4
相关论文
共 26 条
[1]   Biochemical markers of bone metabolism reflect osteoclastic and osteoblastic activity in multiple myeloma [J].
Abildgaard, N ;
Glerup, H ;
Rungby, J ;
Bendix-Hansen, K ;
Kassem, M ;
Brixen, K ;
Heickendorff, L ;
Nielsen, JL ;
Eriksen, EF .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2000, 64 (02) :121-129
[2]   The clinical and prognostic significance of erythrocyte sedimentation rate (ESR), serum interleukin-6 (IL-6) and acute phase protein levels in multiple myeloma [J].
Alexandrakis, MG ;
Passam, FH ;
Ganotakis, ES ;
Sfiridaki, K ;
Xilouri, I ;
Perisinakis, K ;
Kyriakou, DS .
CLINICAL AND LABORATORY HAEMATOLOGY, 2003, 25 (01) :41-46
[3]   New advances in the biology and treatment of myeloma bone disease [J].
Berenson, JR .
SEMINARS IN HEMATOLOGY, 2001, 38 (02) :15-20
[4]  
Bíró L, 1998, EUR J CLIN INVEST, V28, P679
[5]  
Caldera Humberto, 2004, Curr Hematol Rep, V3, P249
[6]  
Filella X, 1996, CANCER DETECT PREV, V20, P52
[7]   Interleukin-6 activates phosphoinositol-30 kinase in multiple myeloma tumor cells by signaling through RAS-dependent and, separately, through p85-dependent pathways [J].
Hsu, JH ;
Shi, YJ ;
Frost, P ;
Yan, HJ ;
Hoang, B ;
Sharma, S ;
Gera, J ;
Lichtenstein, A .
ONCOGENE, 2004, 23 (19) :3368-3375
[8]   Survival and proliferation factors of normal and malignant plasma cells [J].
Klein, B ;
Tarte, K ;
Jourdan, M ;
Mathouk, K ;
Moreaux, J ;
Jourdan, E ;
Legouffe, E ;
De Vos, J ;
Rossi, JF .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2003, 78 (02) :106-113
[9]   High-dose therapy and autologous stem cell transplantation for multiple myeloma poorly responsive to initial therapy [J].
Kumar, S ;
Lacy, MQ ;
Dispenzieri, A ;
Rajkumar, SV ;
Fonseca, R ;
Geyer, S ;
Allmer, C ;
Witzig, TE ;
Lust, JA ;
Greipp, PR ;
Kyle, RA ;
Litzow, MR ;
Gertz, MA .
BONE MARROW TRANSPLANTATION, 2004, 34 (02) :161-167
[10]   Management of patients with multiple myeloma: Emphasizing the role of high-dose therapy [J].
Kyle, RA .
CLINICAL LYMPHOMA, 2001, 2 (01) :21-28