Cytotoxic effects of Eryngium kotschyi and Eryngium maritimum on Hep2, HepG2, Vero and U138 MG cell lines.

Pharm Biol

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine , Ankara , Turkey.

Published: December 2013

Context: Eryngium maritimum L. and the endemic Eryngium kotschyi Boiss. of the Apiaceae family are used for antiinflammatory, antivenom, antinociceptive and diuretic purposes in folk medicine in Turkey.

Objective: This study investigated the cytotoxic effects of the plant extracts belonging to Eryngium L. genus on various cell lines.

Materials And Methods: Cytotoxic activites of the lyophilized aqueous aereal and root parts of the plant extracts on human hepatocellular carcinoma (HepG2), human laryngeal epidermoid carcinoma (Hep2), human glioma (U138-MG) and African green monkey kidney epithelial (Vero) cell lines at 8.33-266.62 µg/ml concentrations were analyzed by lactate dehydrogenase (LDH) leakage and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) cell viability assays.

Results: Inhibitory concentration 50 (IC50) values were found <100 µg/ml in most cases varying around 16.33-125.66 µg/ml. IC50 values for E. kostchyi and E. maritimum root parts on Hep2 cells (32.86 and 30.25 µg/ml, respectively), E. kotschyi aereal, E. maritimum aereal and root parts on HepG2 cells (31.75, 32.42 and 35.01 µg/ml, respectively) by MTT assay were found to be close to the US National Cancer Institute (NCI) recommendations (IC50 < 30 µg/ml) to define the antivity aganist cancer cells. The lowest IC50 values according to the LDH method were observed in Hep2 cells and the highest in U138-MG cells. Root parts were found to be more toxic than aereal parts for both plants in both methods in general.

Discussion And Conclusion: Both plant extracts exerted cytotoxic activity aganist Hep2 and HepG2 cells, with low IC50 values defining their promising anticancer property according to NCI; however, further analysis are needed to confirm their activity.

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Source
http://dx.doi.org/10.3109/13880209.2013.803208DOI Listing

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