Department of Molecular Genetics, University of Lodz, Lodz, Poland.
Arch Toxicol. 2011 Nov;85(11):1453-61. doi: 10.1007/s00204-010-0593-x. Epub 2010 Sep 29.
Bisphenol A-glycidyl methacrylate (BisGMA) is monomer of dental filling composites, which can be released from these materials and cause adverse biologic effects in human cells. In the present work, we investigated genotoxic effect of BisGMA on human lymphocytes and human acute lymphoblastic leukemia cell line (CCRF-CEM) cells. Our results indicate that BisGMA is genotoxic for human lymphocytes. The compound induced DNA damage evaluated by the alkaline, neutral, and pH 12.1 version of the comet assay. This damage included oxidative modifications of the DNA bases, as checked by DNA repair enzymes EndoIII and Fpg, alkali-labile sites and DNA double-strand breaks. BisGMA induced DNA-strand breaks in the isolated plasmid. Lymphocytes incubated with BisGMA at 1 mM were able to remove about 50% of DNA damage during 120-min repair incubation. The monomer at 1 mM evoked a delay of the cell cycle in the S phase in CCRF-CEM cells. The experiment with spin trap-DMPO demonstrated that BisGMA induced reactive oxygen species, which were able to damage DNA. BisGMA is able to induce a broad spectrum of DNA damage including severe DNA double-strand breaks, which can be responsible for a delay of the cell cycle in the S phase.
双酚 A 缩水甘油甲基丙烯酸酯(BisGMA)是牙科填充复合材料的单体,它可以从这些材料中释放出来,并对人体细胞产生不良的生物学影响。在本工作中,我们研究了 BisGMA 对人淋巴细胞和人急性淋巴细胞白血病细胞系(CCRF-CEM)细胞的遗传毒性作用。我们的结果表明,BisGMA 对人淋巴细胞具有遗传毒性。该化合物通过碱性、中性和 pH12.1 版本的彗星试验评估了 DNA 损伤。这种损伤包括 DNA 碱基的氧化修饰,通过 DNA 修复酶 EndoIII 和 Fpg 进行检查,碱不稳定位点和 DNA 双链断裂。BisGMA 诱导分离质粒中的 DNA 链断裂。在 1mM BisGMA 孵育的淋巴细胞在 120 分钟修复孵育期间能够去除约 50%的 DNA 损伤。在 CCRF-CEM 细胞中,浓度为 1mM 的单体使细胞周期在 S 期延迟。自旋捕获-DMPO 的实验表明,BisGMA 诱导了活性氧,能够损伤 DNA。BisGMA 能够诱导广泛的 DNA 损伤,包括严重的 DNA 双链断裂,这可能是导致 S 期细胞周期延迟的原因。