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Xanthorrhizol: a Review of Its Pharmacological Activities and Anticancer Properties

Overview
Journal Cancer Cell Int
Publisher Biomed Central
Date 2015 Oct 27
PMID 26500452
Citations 29
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Abstract

Xanthorrhizol (XNT) is a bisabolane-type sesquiterpenoid compound extracted from Curcuma xanthorrhiza Roxb. It has been well established to possess a variety of biological activities such as anticancer, antimicrobial, anti-inflammatory, antioxidant, antihyperglycemic, antihypertensive, antiplatelet, nephroprotective, hepatoprotective, estrogenic and anti-estrogenic effects. Since many synthetic drugs possess toxic side effects and are unable to support the increasing prevalence of disease, there is significant interest in developing natural product as new therapeutics. XNT is a very potent natural bioactive compound that could fulfil the current need for new drug discovery. Despite its importance, a comprehensive review of XNT's pharmacological activities has not been published in the scientific literature to date. Here, the present review aims to summarize the available information in this area, focus on its anticancer properties and indicate the current status of the research. This helps to facilitate the understanding of XNT's pharmacological role in drug discovery, thus suggesting areas where further research is required.

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References
1.
Yamazaki M, Maebayashi Y, Iwase N, Kaneko T . Studies on pharmacologically active principles from Indonesian crude drugs. I. Principle prolonging pentobarbital-induced sleeping time from Curcuma xanthorrhiza Roxb. Chem Pharm Bull (Tokyo). 1988; 36(6):2070-4. DOI: 10.1248/cpb.36.2070. View

2.
Chung W, Park J, Kim M, Kim H, Hwang J, Lee S . Xanthorrhizol inhibits 12-O-tetradecanoylphorbol-13-acetate-induced acute inflammation and two-stage mouse skin carcinogenesis by blocking the expression of ornithine decarboxylase, cyclooxygenase-2 and inducible nitric oxide synthase through.... Carcinogenesis. 2007; 28(6):1224-31. DOI: 10.1093/carcin/bgm005. View

3.
Noomhorm N, Chang C, Wen C, Wang J, Chen J, Tseng L . In vitro and in vivo effects of xanthorrhizol on human breast cancer MCF-7 cells treated with tamoxifen. J Pharmacol Sci. 2014; 125(4):375-85. DOI: 10.1254/jphs.14024fp. View

4.
Cummings J, Ward T, Ranson M, Dive C . Apoptosis pathway-targeted drugs--from the bench to the clinic. Biochim Biophys Acta. 2004; 1705(1):53-66. DOI: 10.1016/j.bbcan.2004.09.005. View

5.
Wilken R, Veena M, Wang M, Srivatsan E . Curcumin: A review of anti-cancer properties and therapeutic activity in head and neck squamous cell carcinoma. Mol Cancer. 2011; 10:12. PMC: 3055228. DOI: 10.1186/1476-4598-10-12. View