Honokiol: A Novel Natural Agent for Cancer Prevention and Therapy

被引:182
|
作者
Arora, S. [1 ]
Singh, S. [1 ]
Piazza, G. A. [1 ,2 ]
Contreras, C. M. [3 ]
Panyam, J. [4 ]
Singh, A. P. [1 ,2 ]
机构
[1] Univ S Alabama, Dept Oncol Sci, Mitchell Canc Inst, Mobile, AL 36604 USA
[2] Univ S Alabama, Coll Med, Dept Biochem & Mol Biochem, Mobile, AL 36604 USA
[3] Univ S Alabama, Coll Med, Dept Surg, Mobile, AL 36604 USA
[4] Univ Minnesota, Coll Pharm, Dept Pharmaceut, Minneapolis, MN 55455 USA
关键词
Honokiol; chemoprevention; chemotherapy; natural agent; COMBINING LIPOSOMAL HONOKIOL; MAGNOLIA BARK EXTRACT; NF-KAPPA-B; BREAST-CANCER; IN-VITRO; INHIBITS ANGIOGENESIS; NITRIC-OXIDE; APOPTOSIS; GROWTH; ACTIVATION;
D O I
10.2174/156652412803833508
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Honokiol (3',5-di-(2-propenyl)-1,1'-biphenyl-2,4'-diol) is a bioactive natural product derived from Magnolia spp. Recent studies have demonstrated anti-inflammatory, anti-angiogenic, anti-oxidative and anticancer properties of honokiol in vitro and in preclinical models. Honokiol targets multiple signaling pathways including nuclear factor kappa B (NF-kappa B), signal transducers and activator of transcription 3 (STAT3), epidermal growth factor receptor (EGFR) and mammalian target of rapamycin (m-TOR), which have great relevance during cancer initiation and progression. Furthermore, pharmacokinetic profile of honokiol has revealed a desirable spectrum of bioavailability after intravenous administration in animal models, thus making it a suitable agent for clinical trials. In this review, we discuss recent data describing the molecular targets of honokiol and its anti-cancer activities against various malignancies in pre-clinical models. Evaluation of honokiol in clinical trials will be the next step towards its possible human applications.
引用
收藏
页码:1244 / 1252
页数:9
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