Targeting superoxide dismutase to renal proximal tubule cells inhibits nephrotoxicity of cisplatin and increases the survival of cancer-bearing mice

被引:33
作者
Nishikawa, M
Nagatomi, H
Nishijima, M
Ohira, G
Chang, BJ
Sato, E
Inoue, M
机构
[1] Osaka City Univ, Sch Med, Dept Biochem, Abeno Ku, Osaka 5458585, Japan
[2] Osaka City Univ, Sch Med, Dept Internal Med, Abeno Ku, Osaka 5458585, Japan
关键词
cancer; cis-diamminedichloroplatinum(II); oxidative stress; kidney; hexamethylenediamine-conjugated superoxide dismutase;
D O I
10.1016/S0304-3835(01)00591-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because cis-diamminedichloroplatinum(II) (cisplatin) which generates reactive oxygen species induces renal dysfunction, administration of a large dose for killing cancer cells is highly limited. We recently synthesized a cationic superoxide dismutase (SOD) (hexamethylenediamine-conjugated SOD, AH-SOD) which rapidly accumulates in renal proximal tubule cells and inhibits oxidative injury of the kidney. Treatment of Ehrlich ascites tumor cells (EATC)-bearing mice with cisplatin sufficient for killing tumor cells increased their motality. The motality of cisplatin-treated EATC-bearing mice was markedly decreased by AH-SOD. These results suggest that targeting SOD to renal proximal tubule cells might permit the administration of high doses of cisplatin and related anticancer agents without causing renal injury, (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:133 / 138
页数:6
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