4.7 Article

Catalytic inhibition of human DNA topoisomerase II by interactions of grape cell culture polyphenols

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 54, 期 6, 页码 2083-2087

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jf052700z

关键词

chemopreventive agents; grape cell culture; isobolographic analysis; resveratrol; synergistic interactions; topoisomerase II catalytic inhibition; Vitis

资金

  1. NCCIH NIH HHS [P50 AT-00477] Funding Source: Medline

向作者/读者索取更多资源

Previously, we isolated mixed polyphenolic fractions on a toyopearl matrix (TP-2 to TP-6) from grape cell cultures that were highly potent catalytic inhibitors in a human DNA topoisomerase 11 assay for cancer chemoprevention. The objectives of this study were to evaluate the potency of, and potential interactions between, individual fractions and some of the purified bioactive polyphenols that comprise these fractions on human DNA topoisomerase 11 catalytic activity. Treatments that combined anthocyan in-rich fractions (TP-2; 0.5 or 2.0 mu g of dried material/mL), fractions containing catechins, procyanidin dimers, and flavanones (TP-4; 0.25 mu g of dried material/mL), and/or fractions enriched with procyanidin oligomers and polymers (TP-6; 0.15 or 0.5 mu g of dried material/mL) showed additive effects toward catalytic inhibition of the enzyme. Epicatechin gallate (IC50 = 0.029 mu M), myricetin (0.39 mu M), procyanidin B-2 (PB2, 4.5 mu M), and resveratrol (65.7 mu M), constituents of the most bioactive mixed fraction from grape cell culture (TP-4), each individually provided potent catalytic inhibition of topoisomerase II. In addition, potentiating interactions between the PB2 and the other polyphenolic constituents mentioned above and between myricetin and resveratrol were clearly demonstrated. A synergistic interaction between myricetin and resveratrol was also confirmed with isobolographic analysis at a molar ratio of 1:70.

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