Home Neoplasma 2005 Neoplasma Vol.52, p.510-516, 2005

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Founded: 1954
ISSN 0028-2685
ISSN 1338-4317 (online)

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Neoplasma Vol.52, p.510-516, 2005

Title: Enhanced sensitivity of human ovarian carcinoma cell lines A2780 and A2780/CP to the combination of cisplatin and synthetic isothiocyanate ethyl 4-isothiocyanatobutanoate
Author: J., BODO ; J., CHOVANCOVA ; L., HUNAKOVA ; J., SEDLAK ;

Abstract: Naturally occurring and synthetic isothiocyanates (ITCs) are known as chemopreventive agents. The present study shows a new synthetic ITC derivate ethyl 4-isothiocyanatobutanoate (E- 4IB) as an effective modulator of cellular proliferation and inducer of apoptosis with potential utility as an anticancer drug, as well as a sensitizer to routinely used chemotherapeutic agent cisplatin (cis-Pt). Evaluation of the growth inhibitory effects of E-4IB in the human ovarian carcinoma cell line A2780 and its cisplatin-resistant variant A2780/CP using MTT-test and its apoptosis-inducing properties by flow cytometry was performed. Effect of E-4IB was assessed both alone and in paired combination with cisplatin. Combination index (CI) values from Calcusyn software were used to characterize the interactions as synergistic, additive, or antagonistic. Significant synergistic effect in growth inhibition of E-4IB (0.5–5 µM) with cis-Pt (2.5–10 µM) on A2780 parental cell line (CI from 0.39 to 0.75) was also observed on A2780/CP resistant subline, although to a lesser extent (CI from 0.43 to 0.86) for cis-Pt concentrations 5–25 µM and the same concentrations of E-4IB. Synergy in growth inhibition correlated with the potential of E-4IB to stimulate apoptosis induced by cis-Pt (from 9.5% to 24.7% at 24 hours) while E-4IB alone induced 3.6% of apoptotic cells in A2780 cell line. We conclude that E-4IB may be worth of further studies assessing its value in the ovarian carcinoma treatment, in combination with the other chemotherapeutic agents.

Keywords: ovarian carcinoma, isothiocyanate, cisplatin, growth inhibition, apoptosis
Year: 2005, Volume: 52, Issue: Page From: 510, Page To: 516

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