Prognostic significance of metallothionein in B-cell lymphomas

被引:33
作者
Poulsen, Christian Bjorn
Borup, Rehannah
Borregaard, Niels
Nielsen, Finn Cilius
Moller, Michael Boe
Ralfkiaer, Elisabeth
机构
[1] Copenhagen Univ Hosp, Rigshosp, Dept Pathol, DK-2100 Copenhagen KBH 0, Denmark
[2] Copenhagen Univ Hosp, Rigshosp, Dept Clin Biochem, DK-2100 Copenhagen KBH 0, Denmark
[3] Copenhagen Univ Hosp, Dept Hematol, DK-2100 Copenhagen KBH 0, Denmark
[4] Odense Univ Hosp, Dept Pathol, DK-5000 Odense, Denmark
关键词
D O I
10.1182/blood-2006-04-015305
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We have investigated metallothionein (MT) I and II mRNA and protein in B-cell lymphomas with particular reference to diffuse large B-cell lymphoma (DLBCL). The mRNA profiling was performed on Affymetrix arrays and showed up-regulated MT mRNA in 15 of 48 DLBCLs, including 12 of 23 activated B-cell (ABC) and 3 of 9 type-3 lesions. In contrast, MT mRNA was low to undetectable in 16 germinal center B-cell (GCB)-type DLBCLs. Only 1 of 15 patients with up-regulated MT mRNA achieved a sustained remission, suggesting that up-regulated MT mRNA constitutes a significant risk factor for treatment failure. This was confirmed in 2 independent series, which showed significantly shorter 5-year survival in DLBCL with high versus low MT-IIa levels. By immunohistology, MT was shown to be present in both macrophages and lymphoma cells. The proportion of MT-positive macrophages did not correlate with the survival. In contrast, in 115 DLBCLs, MT labeling of more than 20% lymphoma cells was associated with a significantly poorer 5-year survival, independent of the age, stage, or International Prognostic Index. Taken together, it is suggested that both increased MT mRNA and MT protein expression by more than 20% lymphoma cells constitute independent risk factors in DLBCL.
引用
收藏
页码:3514 / 3519
页数:6
相关论文
共 39 条
[1]
Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[2]
Metallothioneins in human tumors and potential roles in carcinogenesis [J].
Cherian, M. George ;
Jayasurya, A. ;
Bay, Boon-Huat .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 533 (1-2) :201-209
[3]
Zinc homeostasis-regulating proteins: New drug targets for triggering cell fate [J].
Chimienti, F ;
Aouffen, M ;
Favier, A ;
Seve, M .
CURRENT DRUG TARGETS, 2003, 4 (04) :323-338
[4]
Metallothionein: The multipurpose protein [J].
Coyle, P ;
Philcox, JC ;
Carey, LC ;
Rofe, AM .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (04) :627-647
[5]
ATM mutations are associated with inactivation of the ARF-TP53 tumor suppressor pathway in diffuse large B-cell lymphoma [J].
Gronbæk, K ;
Worm, J ;
Ralfkiaer, E ;
Ahrenkiel, V ;
Hokland, P ;
Guldberg, P .
BLOOD, 2002, 100 (04) :1430-1437
[6]
Concurrent disruption of p16INK4a and the ARF-p53 pathway predicts poor prognosis in aggressive non-Hodgkin's lymphoma [J].
Gronbæk, K ;
Brown, PD ;
Moller, MB ;
Nedergaard, T ;
Ralfkiaer, E ;
Moller, P ;
Zeuthen, J ;
Guldberg, P .
LEUKEMIA, 2000, 14 (10) :1727-1735
[7]
He T, 2000, CELL MOL BIOL, V46, P383
[8]
Prognostic significance of bcl-2 protein expression in aggressive non-Hodgkin's lymphoma [J].
Hermine, O ;
Haioun, C ;
Lepage, E ;
dAgay, MF ;
Briere, J ;
Lavignac, C ;
Fillet, G ;
Salles, G ;
Marolleau, JP ;
Diebold, J ;
Reyes, F ;
Gaulard, P .
BLOOD, 1996, 87 (01) :265-272
[9]
Metallothionein expression and oxidative stress in the brain [J].
Hidalgo, J ;
Penkowa, M ;
Giralt, M ;
Carrasco, J ;
Molinero, A .
PROTEIN SENSORS AND REACTIVE OXYGEN SPECIES, PT B, THIOL ENZYMES AND PROTEINS, 2002, 348 :238-249
[10]
Jaffe ES., 2001, PATHOLOGY GENETICS T