首页> 美国卫生研究院文献>Journal of Oncology >Short-Term Exposure to Tobacco Toxins Alters Expression ofMultiple Proliferation Gene Markers in Primary Human BronchialEpithelial Cell Cultures
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Short-Term Exposure to Tobacco Toxins Alters Expression ofMultiple Proliferation Gene Markers in Primary Human BronchialEpithelial Cell Cultures

机译:短期接触烟草毒素会改变的表达原发性人类支气管中的多个增殖基因标记上皮细胞培养

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摘要

The biological effects of only a finite number of tobacco toxins have been studied. Here, we describe exposure of cultures of human bronchial epithelial cells to low concentrations of tobacco carcinogens: nickel sulphate, benzo(b)fluoranthene, N-nitrosodiethylamine, and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). After a 24-hour exposure, EGFR was expressed in cell membrane and cytoplasm, BCL-2 was expressed only in the irregular nuclei of large atypical cells, MKI67 was expressed in nuclei with no staining in larger cells, cytoplasmic BIRC5 with stronger nuclear staining was seen in large atypical cells, and nuclear TP53 was strongly expressed in all cells. After only a 24-hour exposure, cells exhibited atypical nuclear and cytoplasmic features. After a 48-hour exposure, EGFR staining was localized to the nucleus, BCL-2 was slightly decreased in intensity, BIRC5 was localized to the cytoplasm, and TP53 staining was increased in small and large cells. BCL2L1 was expressed in both the cytoplasm and nuclei of cells at 24- and 48-hour exposures. We illustrate that short-termexposure of a bronchial epithelial cell line to smoking-equivalent concentrations of tobacco carcinogens alters the expression of key proliferation regulatory genes, EGFR, BCL-2, BCL2L1, BIRC5, TP53, and MKI67, similar to that reported in biopsy specimens of pulmonary epithelium described to be preneoplastic lesions.
机译:仅对有限数量的烟草毒素的生物学效应进行了研究。在这里,我们描述了人类支气管上皮细胞培养物对低浓度烟草致癌物的暴露:硫酸镍,苯并(b)荧蒽,N-亚硝基二乙胺和4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)。暴露24小时后,EGFR在细胞膜和细胞质中表达,BCL-2仅在大的非典型细胞的不规则核中表达,MKI67在细胞核中表达,在较大细胞中不染色,胞浆BIRC5的核染色更强。在大型非典型细胞中可见,而核TP53在所有细胞中均强烈表达。仅暴露24小时后,细胞显示出非典型的核和细胞质特征。暴露48小时后,EGFR染色位于细胞核内,BCL-2的强度略有降低,BIRC5位于细胞质内,TP53染色在大小细胞中均增加。在暴露24和48小时后,BCL2L1在细胞质和细胞核中均表达。我们举例说明,支气管上皮细胞系短期暴露于吸烟等浓度的烟草致癌物会改变关键增殖调节基因,EGFR,BCL-2,BCL2L1,BIRC5,TP53和MKI67的表达,与活检中报道的相似肺上皮标本描述为肿瘤前病变。

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