首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Evaluation of the genotoxicity of the phytoestrogen, coumestrol, in AHH-1 TK+/- human lymphoblastoid cells
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Evaluation of the genotoxicity of the phytoestrogen, coumestrol, in AHH-1 TK+/- human lymphoblastoid cells

机译:评价植物雌激素香豆酚对AHH-1 TK +/-人淋巴母细胞的遗传毒性

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Coumestrol, a phytoestrogen found in high levels in alfalfa and red clover, is of concern since endocrine disorders have been observed in farm animals exposed to high levels of phytoestrogens. Previous studies found that coumestrol was an effective inducer of DNA strand breaks, micronuclei, and mutations in the Hypoxanthine phosphoribosyl transferase (HPRT) gene of Chinese hamster ovary cells. In the experiments presented here, we extended the previous studies to examine the effect of coumestrol exposure on AHH-1 TK+/- human lymphoblastoid cells. Micronuclei were induced with the highest frequency occurring at day ? after exposure. Flow cytometric analysis of annexin V-FITC-7-aminoactinomycin D stained cells indicated that the primary pathway of cell death was by apoptosis. Mutations were induced in the Thymidine Kinase (TK) gene and were due primarily to the induction of clones with the slow-growth phenotype. Subsequent molecular analysis revealed the loss of exon 4 in the coumestrol-induced clones. indicative of loss-of heterozygosity and consistent with a proposed inhibition of topoisomerase-II activity as a mechanism of action for coumestrol. Taken together, these results suggest that coumestrol exhibits both mutagenic and clastogenic properties in cultured human lymphoblastoid cells. Published by Elsevier Science B.V. [References: 37]
机译:香豆酚是在苜蓿和红三叶草中高水平发现的一种植物雌激素,由于人们已在暴露于高水平植物雌激素的农场动物中观察到内分泌失调,因此值得关注。以前的研究发现,香豆酚是中国仓鼠卵巢细胞DNA链断裂,微核和次黄嘌呤磷酸核糖基转移酶(HPRT)基因突变的有效诱导剂。在此处介绍的实验中,我们扩展了先前的研究,以检查香豆酚暴露对AHH-1 TK +/-人淋巴母细胞的影响。微核诱导发生的频率最高的是第2天。接触后。 Annexin V-FITC-7-氨基放线菌素D染色细胞的流式细胞仪分析表明,细胞死亡的主要途径是细胞凋亡。胸腺嘧啶激酶(TK)基因中诱导了突变,这主要归因于具有慢速生长表型的克隆的诱导。随后的分子分析揭示了香豆酚诱导的克隆中外显子4的丢失。指示杂合性丧失,并与拟议的拓扑异构酶-II活性抑制作用(作为香豆酚的作用机制)相一致。综上所述,这些结果表明香豆酚在培养的人淋巴母细胞中既具有诱变特性又具有致裂特性。由Elsevier Science B.V.发布[参考:37]

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