3β,5α,6β-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function

被引:24
作者
Liu, Tao-Fang [1 ,2 ]
Lu, Xin [3 ]
Tang, Hua [1 ,2 ]
Zhang, Min-Min [4 ]
Wang, Pan [1 ,2 ]
Sun, Peng [1 ,2 ]
Liu, Zhi-Yong [3 ]
Wang, Zeng-Lei [1 ,2 ]
Li, Ling [1 ,2 ]
Rui, Yao-Cheng [1 ,2 ]
Li, Tie-Jun [1 ,2 ]
Zhang, Wen [1 ,2 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Res Ctr Marine Drugs, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Dept Pharmacol, Shanghai 200433, Peoples R China
[3] Second Mil Med Univ, Changhai Hosp, Dept Urol, Shanghai 200433, Peoples R China
[4] Anhui Univ Tradit Chinese Med, Sch Pharm, Hefei 230038, Peoples R China
关键词
3; beta; 5; alpha; 6 beta-Oxygenated sterols; Tumor cell growth inhibition; Structure elucidation; Structure-activity; Apoptosis; Muriceopsis flavida; SOFT CORAL; ALCYONACEAN METABOLITES; MARINE STEROLS; POLYHYDROXYLATED STEROLS; BRIARANE DITERPENOIDS; SECONDARY METABOLITES; METHYL SPONGOATE; POLYHYDROXYSTEROLS; INVERTEBRATES;
D O I
10.1016/j.steroids.2012.10.003
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
Three new polyhydroxysterols, named muriflasteroids A-C (1-3) were isolated from the South China Sea gorgonian Muriceopsis flavida, together with sixteen known analogs, cholest-3 beta,5 alpha,6 beta-triol,3 beta-acetate (4), 5 alpha-methoxycholest-3 beta,6 beta-diol (5), (22E)-cholest-22-en-3 beta,5 alpha,6 beta-triol (6), cholest-3 beta,5 alpha,6 beta-triol (7), (22E)-24-norcholest-22-en-3 beta,5 alpha,6 beta-triol (8), (22E,24S)-ergost-22-en-3 beta,5 alpha,6 beta-triol (9), ergost-24(28)-en-3 beta,5 alpha,6 beta-triol (10), (22E)-cholest-7,22-dien-3 beta,5 alpha,6 beta-triol (11), cholest-7-en-3 beta,5 alpha,6 beta-triol (12), (22E)-24-norcholest-7,22-dien-3 beta,5 alpha,6 beta-triol (13), ergost-7,24(28)-dien-3 beta,5 alpha,6 beta-triol (14), (22E,24R)-ergost-7,22-dien-3 beta,5 alpha,6 beta-triol (15), (22E)-cholest-22-en-1 beta,3 beta,5 alpha,6 beta-tetrol (16), (22E)-24-norcholest-22-en-1 beta,3 beta,5 alpha,6 beta-tetrol (17), cholest-1 beta,3 beta,5 alpha,6 beta-tetrol (18), and (24 xi)-ergost-1 beta,3 beta,5 alpha,6 beta-tetrol (19). The structures of the new compounds were elucidated by detailed spectroscopic analysis in combination with comparison of reported data. All the compounds are reported for the first time from the animal. In the bioassay in vitro, these compounds exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. In particular, compound 18 displayed a considerable activity, being similar as that of positive control adriamycin. An annexin V analysis indicated that compounds 7 and 18 can significantly induce apoptosis in A549 cell, and compound 7 is more potent in the induction of apoptosis. Preliminary structure-activity analysis suggests that the acetylation on 3-OH and appearance of Delta(7) may decrease the activity while substitution of 1-OH and the nature of side chain may also play an important role in the activity. Methylation of 5-OH contributed a little to the activity. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 114
页数:7
相关论文
共 45 条
[1]   Marine natural products [J].
Blunt, John W. ;
Copp, Brent R. ;
Keyzers, Robert A. ;
Munro, Murray H. G. ;
Prinsep, Michele R. .
NATURAL PRODUCT REPORTS, 2012, 29 (02) :144-222
[2]   ACID CATALYSED REACTIONS OF 5ALPHA-HYDROXY-STEROIDS .3. WESTPHALEN REARRANGEMENT [J].
BLUNT, JW ;
FISCHER, A ;
HARTSHOR.MP ;
JONES, FW ;
KIRK, DN ;
YOONG, SW .
TETRAHEDRON, 1965, 21 (06) :1567-&
[3]   Selective Cytotoxicity of Oxysterols through Structural Modulation on Rings A and B. Synthesis, in Vitro Evaluation, and SAR [J].
Carvalho, Joao F. S. ;
Manuel Cruz Silva, M. ;
Moreira, Joao N. ;
Simoes, Sergio ;
Luisa Sa e Melo, M. .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (18) :6375-6393
[4]   Efficient trans-diaxial hydroxylation of Δ5-steroids [J].
Carvalho, Joao F. S. ;
Cruz Silva, M. Manuel ;
Sa e Melo, M. Luisa .
TETRAHEDRON, 2010, 66 (13) :2455-2462
[5]   Intrapopulation Variability in the Terpene Metabolism of the Antarctic Opisthobranch Mollusc Austrodoris kerguelenensis [J].
Cutignano, Adele ;
Zhang, Wen ;
Avila, Conxita ;
Cimino, Guido ;
Fontana, Angelo .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 2011 (27) :5383-5389
[6]  
DANNENBERG H, 1964, LIEBIGS ANN CHEM, V674, P152
[7]  
ENDO Y, 1994, CHEM PHARM BULL, V42, P462
[8]   Synthesis and antitumor evaluation of methyl spongoate analogs [J].
Jiang, Cheng-Shi ;
Huang, Cai-Guo ;
Feng, Bo ;
Li, Jia ;
Gong, Jing-Xu ;
Kurtan, Tibor ;
Guo, Yue-Wei .
STEROIDS, 2010, 75 (13-14) :1153-1163
[9]   Drug Transporter-independent Liver Cancer Cell Killing by a Marine Steroid Methyl Spongoate via Apoptosis Induction [J].
Jiang, Yi ;
Miao, Ze-Hong ;
Xu, Lei ;
Yu, Bing ;
Gong, Jing-Xu ;
Tong, Lin-Jiang ;
Chen, Yi ;
Zhou, Zhao-Li ;
Liu, Hong-Chun ;
Wang, Yi ;
Guo, Yue-Wei ;
Ding, Jian .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (30) :26461-26469
[10]  
KOBAYASHI M, 1983, CHEM PHARM BULL, V31, P1848