首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >A comparison of gene expression changes in response to diethylstilbestrol treatment in wild-type and p53+/- hemizygous knockout mice using focussed arrays.
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A comparison of gene expression changes in response to diethylstilbestrol treatment in wild-type and p53+/- hemizygous knockout mice using focussed arrays.

机译:使用聚焦阵列比较野生型和p53 +/-半合子敲除小鼠中对己烯雌酚处理的基因表达变化的比较。

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摘要

We have investigated the hepatic response of female C57BL/6J wild-type and p53(+/-) hemizygous mice to genotoxic levels of diethylstilbestrol (DES) using cell cycle and apoptosis-focussed cDNA expression arrays. DES induced the expression of 12 genes (bad, bax, bcl-x, caspase-1, p53, cyclin D3, GADD45, p21, p15, p27, p57 and Skp1) and down-regulated the expression of eight genes (bcl-2, caspase-2, caspase-7, caspase-8, E124, iNOS, mdm2 and NFkappab1) at twofold or greater levels. Taken together, these changes were strongly reflective of the induction of apoptosis in the livers of DES-treated mice. Of those genes showing the greatest changes in response to DES, p53, p21 and p57 were expressed at 2.1, 1.7 and 1.6 times greater (respectively) in wild-type mice as compared with p53(+/-) hemizygous mice. Differences in p53, p21 and bax expression were confirmed by RT-PCR and we conclude that the compromised response of p53(+/-) mice is likely to play a central role in the earlier appearance of tumours in this model, following exposure to genotoxic carcinogens.
机译:我们已经调查了雌性C57BL / 6J野生型和p53(+/-)半合子小鼠对遗传毒性水平的己烯雌酚(DES)的肝反应,使用细胞周期和凋亡集中的cDNA表达阵列。 DES诱导了12个基因(坏,bax,bcl-x,caspase-1,p53,细胞周期蛋白D3,GADD45,p21,p15,p27,p57和Skp1)的表达,并下调了8个基因(bcl-2 ,caspase-2,caspase-7,caspase-8,E124,iNOS,mdm2和NFkappab1)以两倍或更高的水平。综上所述,这些变化强烈反映了DES治疗小鼠肝脏中细胞凋亡的诱导。在那些对DES反应最大的基因中,与p53(+/-)半合子小鼠相比,p53,p21和p57在野生型小鼠中的表达分别高2.1、1.7和1.6倍。 RT-PCR证实了p53,p21和bax表达的差异,我们得出的结论是,暴露于基因毒性后,p53(+/-)小鼠的受损反应可能在此模型中肿瘤的早期出现中起核心作用致癌物。

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