Cytotoxicity of psammaplin A from a two-sponge association may correlate with the inhibition of DNA replication

• Published in: BMC cancer 2004-09, Vol.4 (1), p.70-70, Article 70
• Main Authors: Jiang, Yahong, Ahn, Eun-Young, Ryu, Seung Hee, Kim, Dong-Kyoo, Park, Jang-Su, Yoon, Hyun Joo, You, Song, Lee, Burm-Jong, Lee, Dong Seok, Jung, Jee H
• Format: Article
• Language: English
• Subjects: Animals; Cell Line, Tumor; Cell Survival - drug effects; Disulfides - pharmacology; DNA Polymerase I - antagonists & inhibitors; DNA Primase - antagonists & inhibitors; DNA Replication - drug effects; Drug Screening Assays, Antitumor; Porifera - chemistry; Simian virus 40; Simian virus 40 - drug effects; Simian virus 40 - physiology; Topoisomerase II Inhibitors; Tyrosine - analogs & derivatives; Tyrosine - pharmacology; Virus Replication - drug effects; Virus Replication - genetics
• ISSN: 1471-2407; 1471-2407
• DOI: 10.1186/1471-2407-4-70

SV40 DNA replication system is a very useful tool to understand the mechanism of replication, which is a tightly regulated process. Many environmental and cellular factors can induce cell cycle arrest or apoptosis by inhibiting DNA replication. In the course of our search for bioactive metabolites from the marine sponges, psammaplin A was found to have some anticancer properties, the possible mechanism of which was studied. Cell viability was determined by Cell Counting Kit-8 (CCK-8) to count living RAW264.7 cells by combining 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium (WST-8) and 1-methoxy-phenazine methosulfate (1-methoxy-PMS). The effect of psammaplin A on DNA replication was carried out in SV40 DNA replication system in vitro. The activities of topoisomerase I and polymerase alpha-primase were measured by the relaxation of superhelical plasmid DNA and the incorporation of [3H]dTTP to the template respectively. The ssDNA binding activity of RPA was assessed by Gel Mobility Shift Assay (GMSA). We have found that psammaplin A delivers significant cytotoxic activity against the RAW264.7 cell line. It was also found that psammaplin A could substantially inhibit SV40 DNA replication in vitro, in which polymerase alpha-primase is one of its main targets. Taken together, we suggest that psammaplin A-induced cytotoxicity may correlate with its inhibition on DNA replication. Psammaplin A has the potential to be developed as an anticancer drug.