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Sodium Pancratistatin 3,4-O-Cyclic Phosphate, a water soluble synthetic derivative of Pancratistatin, is highly effective in a human colon tumour model

Shnyder, S.D; Cooper, P.A; Millington, N.J; Gill, J.H; Bibby, M.C

Authors

S.D Shnyder

P.A Cooper

N.J Millington

J.H Gill

M.C Bibby



Abstract

Sodium pancratistatin 3,4- O-cyclic phosphate ( 2) is a novel water-soluble synthetic derivative of pancratistatin ( 1), a natural alkaloid constituent of Amaryllidaceae plants, that exhibits good cytostatic and antineoplastic activity but is highly insoluble. Unlike most other natural alkaloids it does not act by binding to tubulin, and its mechanism of action has yet to be fully elucidated. Here the efficacy of 2 in a human colon adenocarcinoma model, DLD-1, and some understanding of its mode of action are investigated. Agreeing with previous studies, low cytotoxicity in vitro was seen for 2 with IC 50's of 253 and 19.7 microM for 1 and 96 h exposures, respectively. However in vivo the compound caused statistically significant tumor growth delays ( p < 0.01) at its maximum tolerated dose, and significant vascular shutdown and tumor necrosis were observed. Like 1, the compound appeared to have an unconventional mechanism of action with no effect on microtubule structure, yet causing a G 2/M block, while it was seen to disrupt mitochondrial function. The mechanism of action of 1 and 2 appears to be similar. Thus compound 2, being considerably more soluble than 1, has good potential as an anticancer agent, and further investigation is warranted.

Citation

Shnyder, S., Cooper, P., Millington, N., Gill, J., & Bibby, M. (2008). Sodium Pancratistatin 3,4-O-Cyclic Phosphate, a water soluble synthetic derivative of Pancratistatin, is highly effective in a human colon tumour model. Journal of Natural Products, 71(3), 321-324. https://doi.org/10.1021/np070477p

Journal Article Type Article
Publication Date Mar 1, 2008
Deposit Date Jan 7, 2013
Journal Journal of natural products.
Print ISSN 0163-3864
Electronic ISSN 1520-6025
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 71
Issue 3
Pages 321-324
DOI https://doi.org/10.1021/np070477p