Effect of dehydrodidemnin B on human colon carcinoma cell lines

Lobo, C.; García-Pozo, S.G.; Núñez de Castro, I.; Alonso, F.J.

Anticancer Research 17(1a): 333-336

1997


ISSN/ISBN: 0250-7005
PMID: 9066673
Document Number: 478060
Didemnins are cytotoxic agents belonging to a depsipeptide family isolated from marine tunicates. In the present study, a new member, dehydrodidemnin B (DDB), isolated from the mediterranean tunicate Aplidium albicans, was used. The effect of the drug on human colon cultured cell lines was tested using multiple approaches: proliferation studies, long term survival after three hours of exposure to DDB by means of a clonogenic assay and the decrease of the protooncogene, ornithine decarboxylase, activity. A dehydrodidemnin B concentration of 10-8 M completely inhibited cell growth. The IC-50 obtained using the MTT proliferation test, indicated that the most proliferative cell line (CT-2) was the most sensitive to the drug. Using a clonogenic assay a clear dose-response was obtained for the three cell lines used; HT-29 cell line showed the minimum survival after 3 hours of dehydrodidemnin B treatment. A dose-dependent decrease in ornithine decarboxylase activity was also observed in three cell lines assayed. The data presented indicate that the dehydrodidemnin B is a potent cytotoxic agent on rapidly dividing human colon cancer cells.

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