Boswellia sacra essential oil induces tumor cell-specific apoptosis and suppresses tumor aggressiveness in cultured human breast cancer cells

被引:123
作者
Suhail, Mahmoud M.
Wu, Weijuan [1 ,2 ]
Cao, Amy [3 ]
Mondalek, Fadee G. [1 ]
Fung, Kar-Ming [1 ,4 ]
Shih, Pin-Tsen [2 ,5 ]
Fang, Yu-Ting [2 ,5 ]
Woolley, Cole [6 ]
Young, Gary [6 ]
Lin, Hsueh-Kung [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Urol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Physiol, Oklahoma City, OK 73104 USA
[3] Univ So Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
[4] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73104 USA
[5] Natl Pingtung Univ Sci & Technol, Dept Food Sci, Pingtung 91207, Taiwan
[6] Young Living Essential Oils, Lihi, UT 84043 USA
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2011年 / 11卷
关键词
ACTIVATED PROTEIN-KINASE; CYCLIN D1; IN-VITRO; ACETYL-11-KETO-BETA-BOSWELLIC ACID; SIGNALING PATHWAYS; TRITERPENE ACIDS; FRANKINCENSE OIL; INHIBITION; RESISTANCE; PHOSPHORYLATION;
D O I
10.1186/1472-6882-11-129
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Gum resins obtained from trees of the Burseraceae family (Boswellia sp.) are important ingredients in incense and perfumes. Extracts prepared from Boswellia sp. gum resins have been shown to possess anti-inflammatory and anti-neoplastic effects. Essential oil prepared by distillation of the gum resin traditionally used for aromatic therapy has also been shown to have tumor cell-specific anti-proliferative and pro-apoptotic activities. The objective of this study was to optimize conditions for preparing Boswellea sacra essential oil with the highest biological activity in inducing tumor cell-specific cytotoxicity and suppressing aggressive tumor phenotypes in human breast cancer cells. Methods: Boswellia sacra essential oil was prepared from Omani Hougari grade resins through hydrodistillation at 78 or 100 degrees C for 12 hours. Chemical compositions were identified by gas chromatography-mass spectrometry; and total boswellic acids contents were quantified by high-performance liquid chromatography. Boswellia sacra essential oil-mediated cell viability and death were studied in established human breast cancer cell lines (T47D, MCF7, MDA-MB-231) and an immortalized normal human breast cell line (MCF10-2A). Apoptosis was assayed by genomic DNA fragmentation. Anti-invasive and anti-multicellular tumor properties were evaluated by cellular network and spheroid formation models, respectively. Western blot analysis was performed to study Boswellia sacra essential oil-regulated proteins involved in apoptosis, signaling pathways, and cell cycle regulation. Results: More abundant high molecular weight compounds, including boswellic acids, were present in Boswellia sacra essential oil prepared at 100 degrees C hydrodistillation. All three human breast cancer cell lines were sensitive to essential oil treatment with reduced cell viability and elevated cell death, whereas the immortalized normal human breast cell line was more resistant to essential oil treatment. Boswellia sacra essential oil hydrodistilled at 100 degrees C was more potent than the essential oil prepared at 78 degrees C in inducing cancer cell death, preventing the cellular network formation (MDA-MB-231) cells on Matrigel, causing the breakdown of multicellular tumor spheroids (T47D cells), and regulating molecules involved in apoptosis, signal transduction, and cell cycle progression. Conclusions: Similar to our previous observations in human bladder cancer cells, Boswellia sacra essential oil induces breast cancer cell-specific cytotoxicity. Suppression of cellular network formation and disruption of spheroid development of breast cancer cells by Boswellia sacra essential oil suggest that the essential oil may be effective for advanced breast cancer. Consistently, the essential oil represses signaling pathways and cell cycle regulators that have been proposed as therapeutic targets for breast cancer. Future pre-clinical and clinical studies are urgently needed to evaluate the safety and efficacy of Boswellia sacra essential oil as a therapeutic agent for treating breast cancer.
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页数:14
相关论文
共 73 条
[1]   Cancer chemopreventive effects and cytotoxic activities of the triterpene acids from the resin of Boswellia carteri [J].
Akihisa, Toshihiro ;
Tabata, Keiichi ;
Banno, Norihiro ;
Tokuda, Harukuni ;
Nishihara, Reiko ;
Nakamura, Yuji ;
Kimura, Yumiko ;
Yasukawa, Ken ;
Suzuki, Takashi .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (09) :1976-1979
[2]   Boswellic acids activate p42MAPK and p38 MAPK and stimulate Ca2+ mobilization [J].
Altmann, A ;
Fischer, L ;
Schubert-Zsilavecz, M ;
Steinhilber, D ;
Werz, O .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (01) :185-190
[3]   Gene amplification and overexpression of CDK4 in sporadic breast carcinomas is associated with high tumor cell proliferation [J].
An, HX ;
Beckmann, MW ;
Reifenberger, G ;
Bender, HG ;
Niederacher, D .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (01) :113-118
[4]   Mechanisms underlying the anti-inflammatory actions of boswellic acid derivatives in experimental colitis [J].
Anthoni, C. ;
Laukoetter, M. G. ;
Rijcken, E. ;
Vowinkel, T. ;
Mennigen, R. ;
Mueller, S. ;
Senninger, N. ;
Russell, J. ;
Jauch, J. ;
Bergmann, J. ;
Granger, D. N. ;
Krieglstein, C. F. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2006, 290 (06) :G1131-G1137
[5]   Anti-inflammatory activities of the triterpene acids from the resin of Boswellia carteri [J].
Banno, Norihiro ;
Akihisa, Toshihiro ;
Yasukawa, Ken ;
Tokuda, Harukuni ;
Tabata, Keiichi ;
Nakamura, Yuji ;
Nishimura, Reiko ;
Kimura, Yumiko ;
Suzuki, Takashi .
JOURNAL OF ETHNOPHARMACOLOGY, 2006, 107 (02) :249-253
[6]  
BARTKOVA J, 1995, ONCOGENE, V10, P775
[7]   CYCLIN D1 PROTEIN EXPRESSION AND FUNCTION IN HUMAN BREAST-CANCER [J].
BARTKOVA, J ;
LUKAS, J ;
MULLER, H ;
LUTZHOFT, D ;
STRAUSS, M ;
BARTEK, J .
INTERNATIONAL JOURNAL OF CANCER, 1994, 57 (03) :353-361
[8]   Akt-induced endocrine therapy resistance is reversed by inhibition of mTOR signaling [J].
Beeram, M. ;
Tan, Q.-T. N. ;
Tekmal, R. R. ;
Russell, D. ;
Middleton, A. ;
deGraffenried, L. A. .
ANNALS OF ONCOLOGY, 2007, 18 (08) :1323-1328
[9]   Characterization of 3α-acetyl-11-keto-α-boswellic acid, a pentacyclic triterpenoid inducing apoptosis in vitro and in vivo [J].
Buechele, Berthold ;
Zugmaier, Waltraud ;
Estrada, Aidee ;
Genze, Felicitas ;
Syrovets, Tatiana ;
Paetz, Christian ;
Schneider, Bernd ;
Simmet, Thomas .
PLANTA MEDICA, 2006, 72 (14) :1285-1289
[10]   BREAST TUMOR-CELL LINES FROM PLEURAL EFFUSIONS [J].
CAILLEAU, R ;
YOUNG, R ;
OLIVE, M ;
REEVES, WJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1974, 53 (03) :661-674