Doxorubicin coupled to lactosaminated albumin inhibits the growth of hepatocellular carcinomas induced in rats by diethylnitrosamine

被引:50
作者
Fiume, L
Bolondi, L
Busi, C
Chieco, P
Kratz, F
Lanza, M
Mattioli, A
Di Stefano, G
机构
[1] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
[2] Univ Bologna, Dept Internal Med & Gastroenterol, Bologna, Italy
[3] St Orsola Malpighi Univ Hosp, CRBA, Bologna, Italy
[4] Tumor Biol Ctr, Freiburg, Germany
关键词
drug targeting; asialoglycoprotein receptor; hepatotropic conjugate of doxorubicin; hepatocellular carcinoma targeted doxorubicin; hepatocellular carcinoma chemotherapy;
D O I
10.1016/j.jhep.2005.02.045
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The hepatocyte receptor for asialoglycoproteins internalizes galactosyl terminating macromolecules which can be used as hepatotropic drug carriers. Since this receptor is also expressed on the cells of well differentiated human hepatocellular carcinomas (HCCs), we studied whether conjugation of doxorubicin (DOXO) with lactosaminated human albumin (L-HSA) increases the drug efficacy on HCCs induced in rats by diethylnitrosamine (DENA). Methods: DENA was given in the drinking water for 8 weeks. One week after the last day of DENA administration, animals were randomly assigned to three groups. Each group was administered with either saline, free or coupled DOXO (1 mu g/g). Rats received 4 weekly intravenous injections. One week after the last administration, rats were killed and HCC development was evaluated by counting the tumor nodules on the surface of hepatic lobes. Results: In rats treated with L-HSA coupled DOXO the number of neoplastic nodules was significantly lower (P < 0.05) than that counted in animals injected with saline or with free DOXO. Coupled DOXO did not decrease body rat weight, which was markedly reduced by the free drug. Conclusions: Conjugation with L-HSA increased the antineoplastic efficacy and decreased the systemic toxicity of DOXO administered to rats with HCCs produced by DENA. (c) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:645 / 652
页数:8
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