首页> 外文期刊>Environmental and molecular mutagenesis. >DNA damage in cytologically normal urothelial cells of patients with a history of urothelial cell carcinoma.
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DNA damage in cytologically normal urothelial cells of patients with a history of urothelial cell carcinoma.

机译:有尿路上皮细胞癌病史的患者的细胞学正常的尿路上皮细胞中的DNA损伤。

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摘要

In order to determine if patients with a history of previous urothelial cell carcinoma (UCC) but with current normal urinary cytology have DNA damage in urothelial cells, the single-cell gel electrophoresis (comet) assay was conducted with cells obtained by urinary bladder washings from 44 patients (28 with a history of previous UCC). Increased DNA damage was observed in cytologically "normal" urothelial cells of patients with a history of UCC when compared with referents with no similar history and after correcting the data for smoking status and age (P < 0.018). Increased DNA damage also correlated with the highest tumor grade, irrespective of time or course of the disease after clinical intervention (Kendall tau correlation, 0.37, P = 0.016). Moreover, aneuploidy, as assessed by DNA content ratio (DCR; 75th/25th percentile of total DNA fluorescence of 50 comets/patient) was unaltered by smoking status, but increased with UCC grade: 1.39 +/- 0.12 (median +/- 95% confidence interval; referents); 1.43 +/- 0.11 (Grade I UCC; P = 0.264, against referents); 1.49 +/- 0.16 (Grade II UCC; P = 0.057); 1.57 +/- 0.16 (Grade III UCC; P = 0.003). Micronucleated urothelial cells (MNC) were also scored on Giemsa-stained routine cytological smears and were found not to correlate with DNA damage or DCR. MNC frequencies were higher for patients with a history of UCC and/or smoking than referents with neither history, but there was no statistical difference between groups. Taken together, these results suggest that the normal-appearing urothelium of patients resected for UCC still harbor genetically unstable cells. Environ. Mol. Mutagen. 40:190-199, 2002.
机译:为了确定既往有尿路上皮细胞癌(UCC)病史但当前尿道细胞学正常的患者在尿路上皮细胞中是否存在DNA损伤,对单细胞凝胶电泳(彗星)法进行了分析,该方法是通过从44位患者(其中28位曾有UCC病史)。与无相似病史的参照对象相比,校正吸烟状态和年龄的数据后,在具有UCC病史的患者的细胞学上“正常”的尿道上皮细胞中观察到DNA损伤增加(P <0.018)。 DNA损伤的增加也与最高的肿瘤等级相关,而与临床干预后疾病的时间或病程无关(Kendall tau相关性,0.37,P = 0.016)。此外,通过DNA含量比率(DCR; 50颗彗星/患者的总DNA荧光的75/25%)评估的非整倍性不受吸烟状况的影响,但随UCC等级增加:1.39 +/- 0.12(中位数+/- 95)置信区间百分比;目标对象); 1.43 +/- 0.11(I UCC等级;对于参考对象,P = 0.264); 1.49 +/- 0.16(二级UCC; P = 0.057); 1.57 +/- 0.16(三级UCC; P = 0.003)。在吉姆萨染色的常规细胞学涂片上也对微核尿道上皮细胞(MNC)进行了评分,发现其与DNA损伤或DCR不相关。有UCC和/或吸烟史的患者的MNC频率高于无病史的患者,但两组之间无统计学差异。综上所述,这些结果表明,切除了UCC的患者正常出现的尿路上皮仍具有遗传不稳定的细胞。环境。大声笑诱变剂。 40:190-199,2002。

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