Please use this identifier to cite or link to this item: https://doi.org/10.3390/md10051126
Title: Biochemical studies of the lagunamides, potent cytotoxic cyclic depsipeptides from the marine cyanobacterium Lyngbya majuscula
Authors: Tripathi, A.
Fang, W. 
Leong, D.T. 
Tan, L.T.
Keywords: Apoptosis
Cyclic depsipeptides
Cytotoxicity
Lagunamides
Marine cyanobacterium
Issue Date: May-2012
Source: Tripathi, A., Fang, W., Leong, D.T., Tan, L.T. (2012-05). Biochemical studies of the lagunamides, potent cytotoxic cyclic depsipeptides from the marine cyanobacterium Lyngbya majuscula. Marine Drugs 10 (5) : 1126-1137. ScholarBank@NUS Repository. https://doi.org/10.3390/md10051126
Abstract: Lagunamides A (1) and B (2) are potent cytotoxic cyclic depsipeptides isolated from the filamentous marine cyanobacterium, Lyngbya majuscula, from Pulau Hantu, Singapore. These compounds are structurally related to the aurilide-class of molecules, which have been reported to possess exquisite antiproliferative activities against cancer cells. The present study presents preliminary findings on the selectivity of lagunamides against various cancer cell lines as well as their mechanism of action by studying their effects on programmed cell death or apoptosis. Lagunamide A exhibited a selective growth inhibitory activity against a panel of cancer cell lines, including P388, A549, PC3, HCT8, and SK-OV3 cells, with IC50 values ranging from 1.6 nM to 6.4 nM. Morphological studies showed blebbing at the surface of cancer cells as well as cell shrinkage accompanied by loss of contact with the substratum and neighboring cells. Biochemical studies using HCT8 and MCF7 cancer cells suggested that the cytotoxic effect of 1 and 2 might act via induction of mitochondrial mediated apoptosis. Data presented in this study warrants further investigation on the mode of action and underscores the importance of the lagunamides as potential anticancer agents. © 2012 by the authors.
Source Title: Marine Drugs
URI: http://scholarbank.nus.edu.sg/handle/10635/63533
ISSN: 16603397
DOI: 10.3390/md10051126
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