School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Mutat Res. 2012 May 15;744(2):117-24. doi: 10.1016/j.mrgentox.2012.01.011. Epub 2012 Mar 3.
Cancer chemoprevention with low-dose combinations of bioactive phytochemicals instead of single agents has been suggested to induce less toxicity and improve efficacy. In this study, we selected four plant food-based phytochemicals, viz. chlorogenic acid (CLA), pelargonidin (PEL), resveratrol (RES) and epigallocatechin gallate (EGCG) to evaluate the in vitro chemoprevention of genotoxic damage in HL-60 cells. These agents were tested either individually or as a combination at two concentrations (with a 10-fold difference) against the genotoxins mitomycin C (MMC), diepoxybutane (DEB) and patulin (PAT). Our preliminary ferric reducing antioxidant power (FRAP) assay demonstrated additive effects when PEL, CLA, RES and EGCG were combined. Results of the cytokinesis-block micronucleus test showed significant protection against genotoxic damage induced by PAT, DEB and MMC when CLA, PEL, RES and EGCG were tested individually. This protective effect of the phytochemicals was not concentration-related. Both low- and high-concentration combinations of CLA, PEL, RES and EGCG showed significant reducing effects on the frequencies of micronuclei induced by PAT, DEB and MMC. However, the micronucleus test did not provide indications of additive or synergistic effects with this combination of phytochemicals. In conclusion, the chemo-preventive effects of PEL, CLA, RES and EGCG against genotoxic damage induced by MMC, DEB and PAT are indicative of a 'saturation effect' when higher concentrations and combinations of these phytochemicals are used.
用低剂量组合的生物活性植物化学物质进行癌症化学预防,而不是使用单一药物,据推测可以降低毒性并提高疗效。在这项研究中,我们选择了四种植物性食物来源的植物化学物质,即绿原酸(CLA)、锦葵素(PEL)、白藜芦醇(RES)和没食子儿茶素没食子酸酯(EGCG),以评估它们对 HL-60 细胞遗传毒性损伤的体外化学预防作用。这些药物以单独或组合的形式(相差 10 倍),在两种浓度下(相差 10 倍),针对遗传毒物丝裂霉素 C(MMC)、二环氧丁烷(DEB)和棒曲霉素(PAT)进行了测试。我们初步的铁还原抗氧化能力(FRAP)测定表明,当 PEL、CLA、RES 和 EGCG 联合使用时,具有相加作用。细胞分裂阻断微核试验的结果表明,当单独测试 CLA、PEL、RES 和 EGCG 时,它们对 PAT、DEB 和 MMC 诱导的遗传毒性损伤具有显著的保护作用。这种植物化学物质的保护作用与浓度无关。CLA、PEL、RES 和 EGCG 的低浓度和高浓度组合均对 PAT、DEB 和 MMC 诱导的微核频率表现出显著的降低作用。然而,微核试验并没有表明这种植物化学物质组合具有相加或协同作用的迹象。总之,PEL、CLA、RES 和 EGCG 对 MMC、DEB 和 PAT 诱导的遗传毒性损伤的化学预防作用表明,当使用更高浓度和这些植物化学物质的组合时,存在“饱和效应”。