Abstract |
This paper describes the powerful cytotoxic action exerted by strychnopentamine (SP), a dimeric indole alkaloid extracted from Strychnos usambarensis Gilg, on B16 melanoma cells and on non- cancer human fibroblasts cultured in vitro. SP strongly inhibits cell proliferation and induces cell death at a relatively low concentration (less than 1 microgram/ml) after 72 h of treatment in the two lines. Incorporation of [3H] thymidine and [3H] leucine by B16 cells significantly decreases after only 1 h of treatment at 0.5 microgram/ml. SP induces the formation of dense lamellar bodies and vacuolization in the cytoplasm, intense blebbing at the cell surface and various cytological alterations leading to cell death.
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Authors | J Quetin-Leclercq, M C De Pauw-Gillet, L Angenot, R Bassleer |
Journal | Chemico-biological interactions
(Chem Biol Interact)
Vol. 80
Issue 2
Pg. 203-16
( 1991)
ISSN: 0009-2797 [Print] Ireland |
PMID | 1934150
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Alkaloids
- Antineoplastic Agents
- strychnopentamine
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Topics |
- Alkaloids
(pharmacology)
- Animals
- Antineoplastic Agents
(pharmacology)
- Cell Line
- Fibroblasts
(drug effects)
- Humans
- Melanoma, Experimental
(genetics, pathology, ultrastructure)
- Mice
- Mice, Inbred C57BL
- Mitotic Index
(drug effects)
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