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Induction of renal metallothionein allows increasing dose of an extensively used antitumor drug, cis-diamminedichloroplatinum.

作者信息

Imura N, Naganuma A, Satoh M, Koyama Y

机构信息

Department of Public Health, School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.

出版信息

Experientia Suppl. 1987;52:655-60. doi: 10.1007/978-3-0348-6784-9_70.

DOI:10.1007/978-3-0348-6784-9_70
PMID:2959559
Abstract

The effect of preadministration of bismuth, a specific potent inducer of renal metallothionein (MT), on the lethal and renal toxicity of cis-DDP, an extensively used antitumor drug containing heavy metal platinum, in mice was investigated. Pretreatment of mice with two s.c. doses of bismuth nitrate (BN; 30 mumol/kg/day) at 24-hr interval prevented the lethal toxicity, the increase in BUN value and the occurrence of diarrhea caused by cis-DDP (35 mumol/kg, s.c.). This protective effect of BN-pretreatment was significantly correlated with increased MT levels in the kidney. The pretreatment of tumor-bearing mice with BN also depressed the lethal and renal toxicity of cis-DDP without compromising its antitumor activity, and allowed the administration of relatively high dose of cis-DDP. Daily five consecutive p.o. preadministration of bismuth subnitrate (BSN), one of the bismuth compounds being in use as a protectant of the gastrointestinal lining, was also effective to depress the lethal toxicity of cis-DDP. Since the effective dose of BSN is not far from that commonly used for men, this treatment will allow the increase in cis-DDP dose, promising a clinical advantage in cancer chemotherapy.

摘要

相似文献

1
Induction of renal metallothionein allows increasing dose of an extensively used antitumor drug, cis-diamminedichloroplatinum.
Experientia Suppl. 1987;52:655-60. doi: 10.1007/978-3-0348-6784-9_70.
2
Prevention of lethal and renal toxicity of cis-diamminedichloroplatinum(II) by induction of metallothionein synthesis without compromising its antitumor activity in mice.通过诱导金属硫蛋白合成预防顺二氯二氨铂(II)的致死性和肾毒性,同时不损害其在小鼠中的抗肿瘤活性。
Cancer Res. 1987 Feb 15;47(4):983-7.
3
Citrate enhances the protective effect of orally administered bismuth subnitrate against the nephrotoxicity of cis-diamminedichloroplatinum.柠檬酸盐可增强口服碱式硝酸铋对顺二氨二氯铂肾毒性的保护作用。
Cancer Chemother Pharmacol. 2004 Jan;53(1):33-8. doi: 10.1007/s00280-003-0706-9. Epub 2003 Oct 7.
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Metallothionein induction prevents toxic side effects of cisplatin and adriamycin used in combination.
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Protective role of metallothionein in renal toxicity of cisplatinum.金属硫蛋白在顺铂肾毒性中的保护作用。
Cancer Chemother Pharmacol. 1997;40(4):358-62. doi: 10.1007/s002800050670.
6
Tissue-specific induction of metallothionein by bismuth as a promising protocol for chemotherapy with repeated administration of cis-diamminedichloroplatinum (II) against bladder tumor.铋对金属硫蛋白的组织特异性诱导作为一种有前景的方案,用于顺二氯二氨铂(II)重复给药治疗膀胱肿瘤的化疗。
Anticancer Res. 1992 Nov-Dec;12(6B):2303-7.
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Effect of bismuth nitrate given in combination with cis-diamminedichloroplatinum(II) on the antitumor activity and renal toxicity of the latter in nude mice inoculated with human bladder tumor.硝酸铋与顺二氯二氨合铂(II)联合给药对接种人膀胱肿瘤的裸鼠体内后者抗肿瘤活性及肾毒性的影响
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Effect of coadministration of selenite on the toxicity and antitumor activity of cis-diamminedichloroplatinum (II) given repeatedly to mice.亚硒酸盐与顺二氯二氨铂(II)联合给药对反复给药小鼠的毒性及抗肿瘤活性的影响。
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Modulation of both cisplatin nephrotoxicity and drug resistance in murine bladder tumor by controlling metallothionein synthesis.通过控制金属硫蛋白的合成来调节顺铂对小鼠膀胱肿瘤的肾毒性和耐药性。
Cancer Res. 1993 Apr 15;53(8):1829-32.
10
Effect of preinduction of metallothionein synthesis on clastogenicity of anticancer drugs in mice.
Mutat Res. 1995 Sep;348(1):37-43. doi: 10.1016/0165-7992(95)90019-5.

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Bismuth adjuvant ameliorates adverse effects of high-dose chemotherapy in patients with multiple myeloma and malignant lymphoma undergoing autologous stem cell transplantation: a randomised, double-blind, prospective pilot study.铋佐剂改善接受自体干细胞移植的多发性骨髓瘤和恶性淋巴瘤患者大剂量化疗的不良反应:一项随机、双盲、前瞻性试点研究。
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Metallothionein and zinc homeostasis during tumor progression. Effect of methotrexate treatment.肿瘤进展过程中的金属硫蛋白与锌稳态。甲氨蝶呤治疗的影响。
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