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DOI: 10.1055/s-2006-951735
Potent Antitumor Activity of 3,4-seco-8βH-Ferna-4(23),9(11)-dien-3-oic Acid (EC-2) and 3,4-seco-Oleana-4(23),18-dien-3-oic Acid (EC-4), Evaluated by an in vitro Human Cancer Cell Line Panel
Publication History
Received: May 8, 2006
Accepted: August 25, 2006
Publication Date:
18 October 2006 (online)
Abstract
3,4-seco-8βH-Ferna-4(23),9(11)-dien-3-oic acid (EC-2) (1) and 3,4-seco-oleana-4(23),18-dien-3-oic acid (EC-4) (2) isolated from the whole herb of Euphorbia chamaesyce L. were evaluated for their anti-tumor activities using a panel including 39 human cancer cell lines (HCC) coupled with a drug sensitivity database. Compounds 1 and 2 showed strong cytotoxicity against the HCC panel, even though alcohols 1a and 2a and methyl esters 1b and 2b were inactive.
References
- 1 Tanaka R, Ida T, Kita S, Kamisako W, Matsunaga S. 3,4-seco-Oleana-8βH-fernadienoic acid and other constituents from Euphorbia chamaesyce . Phytochemistry. 1996; 41 1163-8
- 2 Tanaka R, Ida T, Takaoka Y, Kita S, Kamisako W, Matsunaga S. 3,4-seco-Oleana-4(23),18-dien-3-oic acid and other triterpenes from Euphorbia chamaesyce . Phytochemistry. 1994; 36 129-32
- 3 Wada S, Tanaka R, Iida A, Matsunaga S. In vitro inhibitory effects of DNA topoisomerase II by fernane-type triterpenoids isolated from a Euphorbia genes. Bioorg Med Chem Lett. 1998; 28 1219-23
- 4 Karim R, Iwai S, Morimura K, Wanibuchi H, Tanaka R, Matsunaga S. et al . Lack of modification of rat hepatocarcinogenesis by fernane-type triterpenoids, isolated from a Euphorbia genus. Teratog Carcinog Mutagen. 2002; 22 293-9
- 5 Yamori T, Matsunaga A, Sato S, Yamazaki K, Komi A, Ishizu K. et al . Potent antitumor activity of MS-247, a novel DNA minor groove binder, evaluated by an in vitro and in vivo human cancer cell line panel. Cancer Res. 1999; 59 4042-9
- 6 Paull K D, Shomaker R H, Hodes L, Monks A, Scudiero D A, Rubinstein L. et al . Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithum. J Natl Cancer Inst. 1989; 81 1088-92
- 7 Takada Y, Aggarwal B B. Betulinic acid suppresses carcinogen-induced NF-κB activation through inhibition of IκBa kinase and p65 phosphorylation: abrogation of cyclooxygenase-2 and matrix metalloprotease-9. J Immunol. 2003; 171 3278-86
- 8 Monks A, Scudiero D, Skehan P, Shoemaker R, Paull K, Vistica D. et al . Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J Natl Cancer Inst. 1991; 83 757-66
- 9 Stinson S F, Alley M C, Kopp W C, Fiebig H H, Mullendore L A, Pittman A F. et al . Morphological and immunocytochemical characteristics of human tumor cell lines for use in a disease-oriented anticancer drug screen. Anticancer Res. 1992; 12 1035-53
- 10 Yaguchi S, Fukui Y, Koshimizu I, Yoshimi H, Matsuno T, Gouda H. et al . Antitumor activity of ZSTK474, a new phosphatidylinositol 3-kinase inhibitor. J Natl Cancer Inst. 2006; 98 545-56
Dr. Reiko Tanaka
Department of Medicinal Chemistry
Osaka University of Pharmaceutical Sciences
4-20-1 Nasahara
Takatsuki
Osaka 569-1094
Japan
Phone: +81-72-690-1084
Fax: +81-72-690-1084
Email: tanakar@gly.oups.ac.jp