Drug transporter-independent liver cancer cell killing by a marine steroid methyl spongoate via apoptosis induction.
Ontology highlight
ABSTRACT: Hepatocellular carcinoma (HCC) is inherently resistant to the majority of clinical anticancer drugs. To obtain drugs that can circumvent or evade such inherent drug resistance of HCC, we investigated the effect of the marinely derived steroid methyl spongoate (MESP) on HCC cells. MESP displayed potent cell killing against a panel of six HCC cell lines, independent of their expression of drug transporters. MESP did not change the function of the drug transporters, and its cell killing was not impaired in multidrug-resistant cancer cells overexpressing the transporters. The cell killing of MESP was irrelevant to estrogen or androgen signaling and was not associated with cell cycle progression, inhibition of microtubules, and topoisomerases. In contrast, MESP potently induced apoptosis via ac
SUBMITTER: Jiang Y
PROVIDER: S-EPMC3143610 | biostudies-literature | 2011 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA