Metallothioneins in human kidneys and associated tumors

被引:24
作者
Hellemans, G
Soumillion, A
Proost, P
Van Damme, J
Van Poppel, H
Baert, L
De Ley, M
机构
[1] Katholieke Univ Leuven, Biochem Lab, Dept Chem, B-3001 Heverlee, Belgium
[2] Katholieke Univ Leuven, Rega Inst, Lab Mol Immunol, B-3001 Heverlee, Belgium
[3] Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Div Urol, B-3001 Heverlee, Belgium
关键词
metallothionein; kidney; transitional cell carcinoma; adenocarcinoma; oncofetal marker;
D O I
10.1159/000045425
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Human kidneys and their associated tumors (nonneoplastic kidney tissues from patients with a transitional cell carcinoma or an adenocarcinoma and the adenocarcinomas themselves) were evaluated for their Zn, Cd, and Cu contents as well as for their metallothionein (MT) level. The total Cd content was correlated with the MT content, and both values were significantly decreased in the adenocarcinomas in comparison with the other tissues. After extraction and separation by anion-exchange chromatography, MT-0 was identified in the nonneoplastic tissues from both the adenocarcinomas as well as the transitional cell carcinomas. Since until now MT-0 protein was only found in human fetal liver and in Zn-stimulated human monocytes, a possible role for this isoform as an oncofetal marker is hypothesized. Separation of the isoforms of MT by reversed-phase high-performance liquid chromatography and sequence analysis showed besides MT-1e and MT-1l the isoform-MT-1g, which is not expressed in the healthy kidney, and MT-1k, an isoform which is not yet demonstrated in renal tissues. We conclude that the expression profile of the MT isoforms in the kidney changes due to the presence of a tumor. Copyright (C) 1999 S. Karger AG, Basel.
引用
收藏
页码:331 / 340
页数:10
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