Antineoplastic unsaturated fatty acids from Fijian macroalgae

被引:38
作者
Jiang, Ren-Wang [1 ]
Hay, Mark E. [1 ]
Fairchild, Craig R. [3 ]
Prudhomme, Jacques [4 ]
Le Roch, Karine [4 ]
Aalbersberg, William [5 ]
Kubanek, Julia [1 ,2 ]
机构
[1] Georgia Inst Technol, Sch Biol, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[3] Bristol Myers Squibb Pharmaceut Res Inst, Princeton, NJ 08543 USA
[4] Univ Calif Riverside, Dept Cell Biol & Neurosci, Riverside, CA 92521 USA
[5] Univ S Pacific, Inst Appl Sci, Suva, Fiji
基金
美国国家卫生研究院;
关键词
Hydrolithon reinboldii; Tydemania expeditionis; Alga; Cancer; Marine; Unsaturated fatty acid;
D O I
10.1016/j.phytochem.2008.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phytochemical analysis of Fijian populations of the green alga Tydemania expeditionis led to the isolation of two unsaturated fatty acids, 3(zeta)-hydroxy-octadeca-4(E),6(Z),15(Z)-trienoic acid (1) and 3(zeta)-hydroxy-hexadeca-4(E),6(Z)-dienoic acid (2), along with the known 3(zeta)-hydroxy-octadeca-4(E),6(Z)-dienoic acid (4), Investigations of the red alga Hydrolithon reinboldii led to identification of a glycolipid, lithonoside (3), and five known compounds, 15-tricosenoic acid, hexacosa-5,9-dienoic methyl ester, beta-sitosterol, 10(S)-hydroxypheophytin A, and 10(R)-hydroxypheophytin A. The structures of 1-3 were elucidated by spectroscopic methods (1D and 2D NMR spectroscopy and ESI-MS). Compounds 1, 2, and 4, containing conjugated double bonds, demonstrated moderate inhibitory activity against a panel of tumor cell lines (including breast, colon, lung, prostate and ovarian cells) with IC50 values ranging from 1.3 to 14.4 mu M. The similar cell selectivity patterns of these three compounds suggest that they might act by a common, but unknown, mechanism of action. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2495 / 2500
页数:6
相关论文
共 33 条
[1]   Glycolipids from the red alga Chondria armata (Kutz.) Okamura [J].
Al-Fadhli, Ammar ;
Wahidulla, Solimabi ;
D'Souza, Lisette .
GLYCOBIOLOGY, 2006, 16 (10) :902-915
[2]   Oxylipin profiling of the hypersensitive response in Arabidopsis thaliana -: Formation of a novel oxo-phytodienoic acid-containing galactolipid, arabidopside E [J].
Andersson, Mats X. ;
Hamberg, Mats ;
Kourtchenko, Olga ;
Brunnstrom, Asa ;
McPhail, Kerry L. ;
Gerwick, William H. ;
Goebel, Cornelia ;
Feussner, Ivo ;
Ellerstrom, Mats .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (42) :31528-31537
[3]   Novel, rapid, and inexpensive cell-based quantification of antimalarial drug efficacy [J].
Bennett, TN ;
Paguio, M ;
Gligorijevic, B ;
Seudieu, C ;
Kosar, AD ;
Davidson, E ;
Roepe, PD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (05) :1807-1810
[4]  
Birch Eileen E., 1997, P183
[5]   Identification and total synthesis of novel fatty acids from the Caribbean sponge Calyx podatypa [J].
Carballeira, NM ;
Pagán, M ;
Rodríguez, AD .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (08) :1049-1052
[6]   Terpenoids and Glycolipids from Euphorbiaceae [J].
Cateni, F. ;
Falsone, G. ;
Zilic, J. .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2003, 3 (05) :425-437
[7]  
Cesano A, 1998, ANTICANCER RES, V18, P1429
[8]   Galactolipids rather than phlorotannins as herbivore deterrents in the brown seaweed Fucus vesiculosus [J].
Deal, MS ;
Hay, ME ;
Wilson, D ;
Fenical, W .
OECOLOGIA, 2003, 136 (01) :107-114
[9]  
DEROME AE, 1987, MODERN NMR TECHNIQUE, P270
[10]   Conjugated linoleic acid and oxidative behaviour in cancer cells [J].
Devery, R ;
Miller, A ;
Stanton, C .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2001, 29 :341-344