TY - JOUR
T1 - Cytotoxic activities of hexane, ethyl acetate and butanol extracts of marine sponges from Mauritian Waters on human cancer cell lines
AU - Beedessee, Girish
AU - Ramanjooloo, Avin
AU - Aubert, Geneviève
AU - Eloy, Laure
AU - Surnam-Boodhun, Rashmee
AU - Van Soest, Rob W.M.
AU - Cresteil, Thierry
AU - Marie, Daniel E.P.
PY - 2012
Y1 - 2012
N2 - The ocean is an exceptional source of natural products with many of them exhibiting novel structural features and bioactivity. As one of the most interesting phylum with respect to pharmacological active marine compounds, Poriferas have been investigated widely in the last few decades. A total of 60 organic extracts (hexane, ethyl acetate and butanol) from 20 species of marine sponges from Mauritius were screened at 50μg/ml in an in vitro screening assay against 9 human cancer cell lines. From these tested extracts, many exhibited pronounced cytotoxic effect at least in one of the cell lines and cell type cytotoxic specificity was observed. 27% of ethyl acetate, 11% of hexane and 2% of butanol extracts were found to possess a cytotoxicity ≥75% on 9 different cancer cell lines with the sponges Petrosia sp. 1, Petrosia sp. 2, Pericharax heteroraphis and Jaspis sp. being the most active. Overall, the HL-60 cellsweremuch more sensitive to most of the extracts than the other cell lines. We further evaluated the properties of the ethyl acetate (JDE) and hexane extract (JDH) of one sponge, Jaspis sp. on KB cells. JDE displayed a smaller IC50 than JDH. Clonogenic assay confirmed the antiproliferative effect of both extracts while mitochondrialmembrane potential change and microscopic analysis demonstrated extracts-induced apoptosis. Treatment with 100 ng/ml of JDE led to a significant increase of cells (24 h: 4.02%; 48 h: 26.23%) in sub-G1 phase. The cytotoxic properties of the tested extracts from these sponges suggest the presence of compounds with pharmacological potential and are currently undergoing fractionation to isolate the active constituents.
AB - The ocean is an exceptional source of natural products with many of them exhibiting novel structural features and bioactivity. As one of the most interesting phylum with respect to pharmacological active marine compounds, Poriferas have been investigated widely in the last few decades. A total of 60 organic extracts (hexane, ethyl acetate and butanol) from 20 species of marine sponges from Mauritius were screened at 50μg/ml in an in vitro screening assay against 9 human cancer cell lines. From these tested extracts, many exhibited pronounced cytotoxic effect at least in one of the cell lines and cell type cytotoxic specificity was observed. 27% of ethyl acetate, 11% of hexane and 2% of butanol extracts were found to possess a cytotoxicity ≥75% on 9 different cancer cell lines with the sponges Petrosia sp. 1, Petrosia sp. 2, Pericharax heteroraphis and Jaspis sp. being the most active. Overall, the HL-60 cellsweremuch more sensitive to most of the extracts than the other cell lines. We further evaluated the properties of the ethyl acetate (JDE) and hexane extract (JDH) of one sponge, Jaspis sp. on KB cells. JDE displayed a smaller IC50 than JDH. Clonogenic assay confirmed the antiproliferative effect of both extracts while mitochondrialmembrane potential change and microscopic analysis demonstrated extracts-induced apoptosis. Treatment with 100 ng/ml of JDE led to a significant increase of cells (24 h: 4.02%; 48 h: 26.23%) in sub-G1 phase. The cytotoxic properties of the tested extracts from these sponges suggest the presence of compounds with pharmacological potential and are currently undergoing fractionation to isolate the active constituents.
KW - Bioactive compound
KW - Cytotoxic
KW - Marine sponges
KW - Mauritius
UR - http://www.scopus.com/inward/record.url?scp=84862744131&partnerID=8YFLogxK
U2 - 10.1016/j.etap.2012.05.013
DO - 10.1016/j.etap.2012.05.013
M3 - Article
C2 - 22743579
AN - SCOPUS:84862744131
SN - 1382-6689
VL - 34
SP - 397
EP - 408
JO - Environmental Toxicology and Pharmacology
JF - Environmental Toxicology and Pharmacology
IS - 2
ER -