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The cytotoxic activities of cardiac glycosides from Streptocaulon juventas and the structure-activity relationships
被引:20
|作者:
Xue, Rui
[1
]
Han, Na
[1
]
Ye, Chun
[1
]
Wang, Lihui
[2
]
Yang, Jingyu
[2
]
Wang, Yu
[3
]
Yin, Jun
[1
]
机构:
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Dev & Utilizat Key Lab Northeast Plant Mat, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Life Sci & Biopharmaceut, Shenyang 110016, Peoples R China
[3] Peoples Liberat Army 463 Hosp, Shenyang 110042, Peoples R China
来源:
关键词:
Cardiac glycosides;
Streptocaulon juventas;
Anti-tumor activity;
A549;
NCI-H460;
MRC-5;
CARDENOLIDE GLYCOSIDES;
ANTIPROLIFERATIVE ACTIVITY;
SIGNALING PATHWAYS;
CANCER;
DIGITOXIN;
PROLIFERATION;
APOPTOSIS;
BUFALIN;
DIGITALIS;
D O I:
10.1016/j.fitote.2014.08.008
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
A series of cardiac glycosides were isolated and identified from the anti-tumor fraction of the root of Streptocaulon juventas in previous studies. In the present research, the cytotoxic activities of the 43 cardiac glycosides on three cell lines, human lung A549 adenocarcinoma cell, large cell lung cancer NCI-H460 cell and normal human fetal lung fibroblast MRC-5 cell, were evaluated in vitro. Most of the tested compounds showed potent inhibitory activities toward the three cell lines. Then, the structure-activity relationships were discussed in detail. It was indicated that hydroxyl and acetyl groups at C-16 increased the activity, whereas hydroxyl group at C-1 and C-5 can both increase and decrease the activity. Two glucosyl groups which were connected by C1' -> C6' showed better inhibitory activity against cancer cell lines, while the C1' -> C4' connection showed stronger inhibitory activity against the normal cell line. Also, this is the first report that the activities of these compounds exhibited different variation trends between A549 and NCI-H460 cell lines, which indicated that these compounds could selectively inhibit the cell growth. The results would lay a foundation for further research on new anti-tumor drug development. (C) 2014 Elsevier B.V. All rights reserved.
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页码:228 / 233
页数:6
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