Growth-inhibitory effects of the synthetic retinoid CD437 against ovarian carcinoma models in vitro and in vivo

Abstract

The activity of CD437{6-[3-(1-adamantyl)-4 hydroxyphenyl]-2-naphthalene carboxylic acid}, a relatively selective activator of RAR-γ, was evaluated against four human ovarian-carcinoma cell lines : PE01, PE04 (a Pt-resistant in vivo-derived counterpart of PE01), PE01^CDDP (a Pt-resistant in vitro-derived model of PE01) and PE014. Growth inhibition was observed after 3 and 6 days of exposure to sub-micromolar concentrations as assessed by a reduction in cell number. IC₅₀ values against PE01, PE04, PE01^CDDP and PE014 were 0.09, 0.21, 0.12 and 0.28 μM (day 3) and 0.1, 0.14, 0.07 and 0.17 μM (day 6), respectively. Cisplatin-resistant cell lines were as responsive as cisplatin-sensitive lines, indicating potential activity in resistant disease. CD437 was also evaluated against the PE04 xenograft grown in nude mice using daily doses of 20 (days 0–4) and 10 mg/kg (days 0–4 and 7–11) given either by i.p. delivery or oral administration. Significant growth inhibition (P < 0.05) was obtained for both doses and by both routes. These data provide further support for the view that retinoids have value for the treatment of ovarian cancer.