当前吸烟者的尿液在体外诱导非恶性人类细胞系的中心体畸变和纺锤体缺陷

Ute Gabriel , Michelle Giehl , Wiltrud Haass , Lutz Trojan , Maurice Stephan Michel , Wolf-Karsten Hofmann , Wolfgang Seifarth , Alice Fabarius
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引用次数: 3

摘要

含有大量衍生化学致癌物的烟草烟雾是尿路上皮癌的主要危险因素。这些致癌物可以诱导DNA损伤导致染色体不稳定,这在尿路上皮癌的发生中起着重要作用。可能的机制可能是中心体畸变,它导致纺锤体缺陷,并可能导致遗传不稳定。我们评估了从不吸烟者(NS)和当前吸烟者(CS)的尿液浓度为0 - 50%对正常人类真皮成纤维细胞和正常人类尿路上皮细胞(UROtsa)的细胞增殖、染色体、中心体和纺锤体状态的影响。尿液处理2周后,通过中心体和纺锤体免疫染色和常规细胞遗传学分析细胞培养。将效果与未治疗对照组的结果进行比较。对正常人类真皮成纤维细胞和UROtsa细胞的分析显示,与NS尿液和未处理的对照组相比,CS尿液诱导的中心体畸变值以剂量依赖和细胞系无关的方式增加。中心体改变与纺锤体缺陷和散发性染色体畸变增加有关。这些观察结果表明,CS尿液中的化学致癌物在离体中心体和纺锤体缺陷的起源中起着致病作用,导致染色体不稳定,并可能参与尿路上皮癌的发生。
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Urine from current smokers induces centrosome aberrations and spindle defects in vitro in nonmalignant human cell lines

Tobacco smoke containing numerous derived chemical carcinogens is the main risk factor for urothelial carcinoma. These carcinogens can induce DNA damage leading to chromosomal instability, which plays a fundamental role in urothelial carcinogenesis. Possible mechanisms could be centrosomal aberrations, which cause defective spindles and may be responsible for genetic instability. We evaluated the effect of urine from never smokers (NS) and current smokers (CS) in concentrations of 0 to 50% on cell proliferation, chromosomes, centrosomes, and the spindle status of normal human dermal fibroblasts and normal human urothelial cells (UROtsa). After 2 weeks of urine treatment, cell cultures were analyzed by centrosome and spindle immunostaining and conventional cytogenetics. Effects were compared to results of untreated controls. Analysis of normal human dermal fibroblasts and UROtsa cells revealed that urine from CS induced higher values of centrosome aberrations in a dose-dependent and cell line-independent manner when compared to cultures treated with urine from NS and untreated controls. Centrosomal alterations correlated with spindle defects and an increase of sporadic chromosomal aberrations. The observations suggest a causative role of chemical carcinogens in urine from CS in the origin of centrosome and spindle defects in vitro leading to chromosomal instability and may be involved in urothelial carcinogenesis.

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