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DOI: 10.1055/s-2006-951680
© Georg Thieme Verlag KG Stuttgart · New York
Characterization of 3α-Acetyl-11-keto-α-boswellic Acid, a Pentacyclic Triterpenoid Inducing Apoptosis in vitro and in vivo
Publication History
Received: October 17, 2005
Accepted: August 14, 2006
Publication Date:
04 October 2006 (online)
Abstract
3α-Acetyl-11-keto-α-boswellic acid (3α-acetoxy-11-oxo-olean-12-en-24-oic acid, 1) was synthesized by a radical-type reaction using bromine and 3α-acetyl-α-boswellic acid isolated from the oleo-gum-resin of Boswellia carterii. 1D and 2D NMR (COSY, HMBC, ROESY) at 500 MHz were used for shift assignments and structure verification. The compound investigated is present in a herbal preparation extracted from Boswellia serrata oleo-gum-resin, it inhibits the growth of chemotherapy-resistant human PC-3 prostate cancer cells in vitro and induces apoptosis as shown by activation of caspase 3 and the induction of DNA fragmentation. In addition, compound 1 is active in vivo as shown by inhibition of proliferation and induction of apoptosis in PC-3 prostate cancer cells xenotransplanted onto the chick chorioallantoic membrane.
Key words
Cancer - triterpenoids - NMR - apoptosis
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- Supporting Information .
References
- 1 Heldt M R, Syrovets T, Winking M, Sailer E R, Safayhi H, Ammon H PT. et al . Boswellic acids exhibit cytotoxic effects on brain tumor cells independent from 5-lipoxygenase inhibition. Naunyn Schmiedebergs Arch Pharmacol. 1997; 355 R15
- 2 Hoernlein R F, Orlikowski T, Zehrer C, Niethammer D, Sailer E R, Simmet T. et al . Acetyl-11-keto-β-boswellic acid induces apoptosis in HL-60 and CCRF-CEM cells and inhibits topoisomerase I. J Pharmacol Exp Ther. 1999; 288 613-9
- 3 Syrovets T, Gschwend J E, Büchele B, Laumonnier Y, Zugmaier W, Genze F. et al . Inhibition of IκB kinase activity by acetyl-boswellic acids promotes apoptosis in androgen-independent PC-3 prostate cancer cells in vitro and in vivo . J Biol Chem. 2005; 280 6170-80
- 4 Krohn K, Rao M S, Raman N V, Khalilullah M. High-performance thin layer chromatographic analysis of anti-inflammatory triterpenoids from Boswellia serrata Roxb. Phytochem Anal. 2001; 12 374-6
- 5 Büchele B, Zugmaier W, Simmet T. Analysis of pentacyclic triterpenic acids from frankincense gum resins and related phytopharmaceuticals by high-performance liquid chromatography. Identification of lupeolic acid, a novel pentacyclic triterpene. J Chromatogr B. 2003; 791 21-30
- 6 Büchele B, Simmet T. Analysis of 12 different pentacyclic triterpenic acids from frankincense in human plasma by high-performance liquid chromatography and photodiode array detection. J Chromatogr B. 2003; 795 355-62
- 7 Ganzera M, Khan I A. A reversed phase high performance liquid chromatography method for the analysis of boswellic acids in Boswellia serrata . Planta Med. 2001; 67 778-80
- 8 Büchele B, Zugmaier W, Genze F, Simmet T. High-performance liquid chromatographic determination of acetyl-11-keto-α-boswellic acid, a novel pentacyclic triterpenoid, in plasma using a fluorinated stationary phase and photodiode array detection: application in pharmacokinetic studies. J Chromatogr B. 2005; 829 144-8
- 9 Rosenbaum E, Carducci M A. Pharmacotherapy of hormone refractory prostate cancer: new developments and challenges. Expert Opin Pharmacother. 2003; 4 875-87
- 10 Denmeade S R, Isaacs J T. A history of prostate cancer treatment. Nat Rev Cancer. 2002; 2 389-96
- 11 Lee K H. Anticancer drug design based on plant-derived natural products. J Biomed Sci. 1999; 6 236-50
- 12 Winterstein A, Stein G. Untersuchungen in der Saponinreihe. Zur Kenntnis der Mono-oxy-triterpensäuren. Z Physiol Chem. 1932; 208 9-23
- 13 Wieland T, Sucrow W. Die Praxis des organischen Chemikers. Berlin; Walter de Gruyter 1982: p 197-8
- 14 Burysek L, Syrovets T, Simmet T. The serine protease plasmin triggers expression of MCP-1 and CD40 in human primary monocytes via activation of p38 MAPK and Janus kinase (JAK)/STAT signaling pathways. J Biol Chem. 2002; 277 33 509-17
- 15 Pardhy R S, Bhattacharyya S C. β-Boswellic acid, acetyl-β-boswellic acid, acetyl-11-keto-β-boswellic acid and 11-keto-β-boswellic acid, four pentacyclic triterpene acids from the resin of Boswellia serrata Roxb. Indian J Chem. 1978; 16B 176-8
- 16 Belsner K, Büchele B, Werz U, Syrovets T, Simmet T. Structural analysis of pentacyclic triterpenes from the gum resin of Boswellia serrata by NMR spectroscopy. Magn Reson Chem. 2003; 41 115-22
- 17 Sterk V, Büchele B, Simmet T. Effects of food intake on the bioavailability of boswellic acids from a herbal preparation in healthy volunteers. Planta Med. 2004; 70 1155-60
- 18 Wang X Z, Beebe J R, Pwiti L, Bielawska A, Smyth M J. Aberrant sphingolipid signaling is involved in the resistance of prostate cancer cell lines to chemotherapy. Cancer Res. 1999; 59 5842-8
- 19 Li X, Marani M, Mannucci R, Kinsey B, Adriani F, Nicoletti I. et al . Overexpression of Bcl-xL underlies the molecular basis for resistance to staurosporine-induced apoptosis in PC-3 cells. Cancer Res. 2001; 61 1699-706
- 20 Nicholson D W, Ali A, Thornberry N A, Vaillantcourt J P, Ding C K, Gallant M. et al . Identification and inhibition of the ICE/CED-3 protease necessary for mammalian apoptosis. Nature. 1995; 376 37-43
- 21 Reed J C. Apoptosis-based therapies. Nat Rev Drug Discov. 2002; 1 111-21
- 22 Kunzi-Rapp K, Genze F, Küfer R, Reich E, Hautmann R E, Gschwend J E. Chorioallantoic membrane assay: vascularized 3-dimensional cell culture system for human prostate cancer cells as an animal substitute model. J Urol. 2001; 166 1502-7
- 23 Rajnikant V, Gupta V K, Rangari V D, Bapat S R, Agarwal R B, Gupta R. Crystallographic analysis of acetyl β-boswellic acid. Crystallogr Res Technol. 2001; 36 93-100
Dr. Thomas Simmet
Institute of Pharmacology of Natural Products and Clinical Pharmacology
University of Ulm
Helmholtzstr. 20
89081 Ulm
Germany
Fax: +49-731-500-65602
Email: thomas.simmet@uni-ulm.de
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