Analysis of polymorphism at site-174 G/C of interleukin-6 promoter region in multiple myeloma

被引:19
作者
Duch, C. R. [1 ]
Figueiredo, M. S. [1 ]
Ribas, C. [1 ]
Almeida, M. S. S. [1 ]
Colleoni, G. W. B. [1 ]
Bordin, J. O. [1 ]
机构
[1] Univ Fed Sao Paulo, UNIFESP, Escola Paulista Med, Disciplina Hematol & Hemoterapia, BR-04023900 Sao Paulo, Brazil
关键词
multiple myeloma; interleukin-6; polymorphisms;
D O I
10.1590/S0100-879X2006005000067
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
It is well established that interleukin-6 ( IL-6) is an essential growth factor for multiple myeloma ( MM) and patients with increased IL-6 levels have a poor prognosis. In healthy subjects, the presence of the C allele at a polymorphic site (-174 G/ C) of the IL- 6 gene is related to low IL- 6 levels. In view of the potential association of this particular polymorphism with IL- 6 concentration, and the relevance of IL- 6 in MM pathogenesis, the objective of the present study was to investigate the prevalence of IL- 6 (- 174 G/ C) promoter polymorphism and its association with development of MM in Brazilian individuals. We investigated the prevalence of these alleles in 52 patients and 60 healthy subjects ( matched by age, sex, and race) of a Brazilian population. Thirty patients were male ( 42.4%), 24 ( 46.2%) were white and the median age at diagnosis was 58.5 years ( range: 28 to 84 years). To determine the IL- 6 (- 174 G/ C) polymorphism, molecular analysis was performed by polymerase chain reaction followed by endonuclease restriction digestion. The genotype distributions observed in the group of patients were 4% CC, 42% GC and 54% GG. The C allele frequency was 0.25. These results were similar to the control group, suggesting no impact of this polymorphism on the susceptibility to MM.
引用
收藏
页码:265 / 267
页数:3
相关论文
共 14 条
[1]
Genetic predisposition of the interleukin-6 response to inflammation: Implications for a variety of major diseases? [J].
Bennermo, M ;
Held, C ;
Stemme, S ;
Ericsson, CG ;
Silveira, A ;
Green, F ;
Tornvall, P .
CLINICAL CHEMISTRY, 2004, 50 (11) :2136-2140
[2]
Interleukin-6 gene -174G > C and -572G > C promoter polymorphisms are strong predictors of plasma -: Interleukin-6 levels after coronary artery bypass surgery [J].
Brull, DJ ;
Montgomery, HE ;
Sanders, J ;
Dhamrait, S ;
Luong, L ;
Rumley, A ;
Lowe, GDO ;
Humphries, SE .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (09) :1458-1463
[3]
DURIE BGM, 1975, CANCER, V36, P842, DOI 10.1002/1097-0142(197509)36:3<842::AID-CNCR2820360303>3.0.CO
[4]
2-U
[5]
The interleukin-6 G(-174)C promoter polymorphism does not determine plasma interleukin-6 concentrations in experimental endotoxemia in humans [J].
Endler, G ;
Marsik, C ;
Joukhadar, C ;
Marculescu, R ;
Mayr, F ;
Mannhalter, C ;
Wagner, OF ;
Jilma, B .
CLINICAL CHEMISTRY, 2004, 50 (01) :195-200
[6]
The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis [J].
Fishman, D ;
Faulds, G ;
Jeffery, R ;
Mohamed-Ali, V ;
Yudkin, JS ;
Humphries, S ;
Woo, P .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1369-1376
[7]
Multiple myeloma: Increasing evidence for a multistep transformation process [J].
Hallek, M ;
Bergsagel, PL ;
Anderson, KC .
BLOOD, 1998, 91 (01) :3-21
[8]
INTERLEUKIN-6 IN HUMAN MULTIPLE-MYELOMA [J].
KLEIN, B ;
ZHANG, XG ;
LU, ZY ;
BATAILLE, R .
BLOOD, 1995, 85 (04) :863-872
[9]
A review of the cytokine network in multiple myeloma - Diagnostic, prognostic, and therapeutic implications [J].
Lauta, VM .
CANCER, 2003, 97 (10) :2440-2452
[10]
Quantitation of white cell subpopulations by polymerase chain reaction using frozen whole-blood samples [J].
Lee, TH ;
Sakahara, NS ;
Fiebig, EW ;
Hirschkorn, DF ;
Johnson, DK ;
Busch, MP .
TRANSFUSION, 1998, 38 (03) :262-270