PT - JOURNAL ARTICLE AU - LUISA BENASSI AU - CRISTINA MAGNONI AU - STEFANIA GIUDICE AU - GIORGIA BERTAZZONI AU - MARIA PAOLA COSTI AU - MARCELLA RINALDI AU - ALBERTO VENTURELLI AU - ANDREA COPPI AU - TIZIANA ROSSI TI - Pharmacological and Toxicological Evaluation of a New Series of Thymidylate Synthase Inhibitors as Anticancer Agents DP - 2006 Sep 01 TA - Anticancer Research PG - 3499--3504 VI - 26 IP - 5A 4099 - http://ar.iiarjournals.org/content/26/5A/3499.short 4100 - http://ar.iiarjournals.org/content/26/5A/3499.full SO - Anticancer Res2006 Sep 01; 26 AB - Thymidylate synthase (TS) is responsible for catalysing the de novo biosynthesis of doexythymidine monophosphate and is a target for many anticancer drugs. A series of thymidylate synthase inhibitors (TSIs), synthesised in our laboratory, were submitted to primary anticancer screening by the National Cancer Institute (NCI). Four compounds, 3,3-bis(4-methoxyphenyl)-1H,3H-naphtho[1,8-cd]pyran-1-one (MR7), 6-chloro-3,3-bis(4-hydroxyphenyl)-1H,3H-naphtho[1,8-cd]pyran-1-one (MR21), 3,3-bis(3-fluoro-4-hydroxyphenyl)-1H,3H-naphtho[1,8-cd]pyran-1-one (MR35) and 6-bromo-3,3-bis(3-chloro-4-hydroxyphenyl)-1H,3H-naphtho[1,8-cd]pyran-1-one (MR36), passed the criteria and were automatically scheduled for evaluation against the full panel of 60 human tumour cell lines. In this study, the antiproliferative activity of the substances against SK-MEL-2 cells (from metastatic tissue) and SK-MEL-28 cells (from primary malignant melanoma cells) was investigated. Neutral Red uptake and the MTT test were performed to confirm the results of the NCI, and [3H]-thymidine incorporation was performed as a test of the proliferation rate. Our results indicated that compounds MR21 and MR36 were the most active agents and the [3H]-thymidine test was the best in predicting toxicity against melanoma cells. Copyright© 2006 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved