Synergistic antitumor effects of liposomal honokiol combined with adriamycin in breast cancer models

Honokiol, a novel antitumor agent, could induce apoptosis and inhibit the growth of vascular endothelium in several tumor cell lines and xenograft models. It has been suggested that the antitumor effect of chemotherapy could be increased by combining it with an antiangiogenesis agent in anticancer s...

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Veröffentlicht in:Phytotherapy research 2008-08, Vol.22 (8), p.1125-1132
Hauptverfasser: Hou, Wenli, Chen, Lijuan, Yang, Guangli, Zhou, Hang, Jiang, Qiqi, Zhong, Zhenhua, Hu, Jia, Chen, Xiang, Wang, Xianhuo, Yuan, Yuan, Tang, Minghai, Wen, Jing, Wei, Yuquan
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container_end_page 1132
container_issue 8
container_start_page 1125
container_title Phytotherapy research
container_volume 22
creator Hou, Wenli
Chen, Lijuan
Yang, Guangli
Zhou, Hang
Jiang, Qiqi
Zhong, Zhenhua
Hu, Jia
Chen, Xiang
Wang, Xianhuo
Yuan, Yuan
Tang, Minghai
Wen, Jing
Wei, Yuquan
description Honokiol, a novel antitumor agent, could induce apoptosis and inhibit the growth of vascular endothelium in several tumor cell lines and xenograft models. It has been suggested that the antitumor effect of chemotherapy could be increased by combining it with an antiangiogenesis agent in anticancer strategy. The present study explored the potential to increase the antitumor effect of adriamycin by combining it with honokiol in mouse 4T1 breast cancer models, and the underlining mechanism was investigated. Honokiol was encapsulated in liposomes to improve the water insolubility. In vitro, liposomal honokiol inhibited the proliferation of 4T1 cells via apoptosis and significantly enhanced the apoptosis of 4T1 cells induced by adriamycin. In vivo, the systemic administration of liposomal honokiol and adriamycin significantly decreased tumor growth through increased tumor cell apoptosis compared with either treatment alone. Collectively, these findings suggest that liposomal honokiol may augment the induction of apoptosis in 4T1 cells in vitro and in vivo, and this combined treatment has shown synergistic suppression in tumor progression according to the analysis of isobologram. The present study may be important in future exploration of the potential application of the combined approach in the treatment of breast cancer. Copyright © 2008 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/ptr.2472
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It has been suggested that the antitumor effect of chemotherapy could be increased by combining it with an antiangiogenesis agent in anticancer strategy. The present study explored the potential to increase the antitumor effect of adriamycin by combining it with honokiol in mouse 4T1 breast cancer models, and the underlining mechanism was investigated. Honokiol was encapsulated in liposomes to improve the water insolubility. In vitro, liposomal honokiol inhibited the proliferation of 4T1 cells via apoptosis and significantly enhanced the apoptosis of 4T1 cells induced by adriamycin. In vivo, the systemic administration of liposomal honokiol and adriamycin significantly decreased tumor growth through increased tumor cell apoptosis compared with either treatment alone. Collectively, these findings suggest that liposomal honokiol may augment the induction of apoptosis in 4T1 cells in vitro and in vivo, and this combined treatment has shown synergistic suppression in tumor progression according to the analysis of isobologram. The present study may be important in future exploration of the potential application of the combined approach in the treatment of breast cancer. 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Res</addtitle><description>Honokiol, a novel antitumor agent, could induce apoptosis and inhibit the growth of vascular endothelium in several tumor cell lines and xenograft models. It has been suggested that the antitumor effect of chemotherapy could be increased by combining it with an antiangiogenesis agent in anticancer strategy. The present study explored the potential to increase the antitumor effect of adriamycin by combining it with honokiol in mouse 4T1 breast cancer models, and the underlining mechanism was investigated. Honokiol was encapsulated in liposomes to improve the water insolubility. In vitro, liposomal honokiol inhibited the proliferation of 4T1 cells via apoptosis and significantly enhanced the apoptosis of 4T1 cells induced by adriamycin. In vivo, the systemic administration of liposomal honokiol and adriamycin significantly decreased tumor growth through increased tumor cell apoptosis compared with either treatment alone. 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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects adriamycin
Animals
Antineoplastic Agents, Phytogenic - administration & dosage
Antineoplastic Agents, Phytogenic - pharmacology
Apoptosis - drug effects
Biological and medical sciences
Biphenyl Compounds - administration & dosage
Biphenyl Compounds - pharmacology
breast cancer
Breast Neoplasms - blood supply
Breast Neoplasms - drug therapy
Breast Neoplasms - pathology
Cell Line, Tumor
Cell Proliferation - drug effects
Cell Survival - drug effects
combined therapy
Dose-Response Relationship, Drug
Doxorubicin - administration & dosage
Doxorubicin - pharmacology
Drug Combinations
Drug Screening Assays, Antitumor
Drug Synergism
Drugs, Chinese Herbal - administration & dosage
Drugs, Chinese Herbal - pharmacology
Female
General pharmacology
Lignans - administration & dosage
Lignans - pharmacology
liposomal honokiol
Liposomes
Medical sciences
Mice
Mice, Inbred BALB C
Neovascularization, Pathologic - drug therapy
Neovascularization, Pathologic - metabolism
Neovascularization, Pathologic - pathology
Pharmacognosy. Homeopathy. Health food
Pharmacology. Drug treatments
synergistic
Xenograft Model Antitumor Assays
title Synergistic antitumor effects of liposomal honokiol combined with adriamycin in breast cancer models
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