Abstract |
Scopadulcic acid B (SDB), a tetracyclic diterpenoid isolated from a medicinal plant, Scoparia dulcis L., inhibited the effects of tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) in vitro and in vivo; SDB inhibited TPA-enhanced phospholipid synthesis in cultured cells, and also suppressed the promoting effect of TPA on skin tumor formation in mice initiated with 7,12-dimethylbenz[a] anthracene. The potency of SDB proved to be stronger than that of other natural antitumor-promoting terpenoids, such as glycyrrhetinic acid.
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Authors | H Nishino, T Hayashi, M Arisawa, Y Satomi, A Iwashima |
Journal | Oncology
(Oncology)
1993 Mar-Apr
Vol. 50
Issue 2
Pg. 100-3
ISSN: 0030-2414 [Print] Switzerland |
PMID | 8451033
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anticarcinogenic Agents
- Diterpenes
- Phospholipids
- scopadulcic acid B
- 9,10-Dimethyl-1,2-benzanthracene
- Tetradecanoylphorbol Acetate
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Topics |
- 9,10-Dimethyl-1,2-benzanthracene
- Animals
- Anticarcinogenic Agents
(therapeutic use)
- Cells, Cultured
- Diterpenes
(isolation & purification, therapeutic use)
- Female
- HeLa Cells
- Humans
- Mice
- Mice, Inbred ICR
- Phospholipids
(metabolism)
- Plants, Medicinal
(chemistry)
- Skin Neoplasms
(chemically induced, prevention & control)
- Tetradecanoylphorbol Acetate
(pharmacology)
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