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CpG island methylation of microRNAs is associated with tumor size and recurrence of non-small-cell lung cancer

机译:microRNA的CpG岛甲基化与肿瘤大小和非小细胞肺癌的复发相关

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摘要

We investigated whether the CpG island methylation of certain microRNAs was associated with the clinicopathological features and the prognosis of non-small-cell lung cancer. The methylation of mir-152, -9-3, -124-1, -124-2, and -124-3 was analyzed in 96 non-small-cell lung cancer specimens using a combined bisulfite restriction analysis. The median observation period was 49.5months. The methylation of mir-9-3, -124-2, and -124-3 was individually associated with an advanced T factor independent of age, sex, and smoking habit. Moreover, the methylation of multiple microRNA loci was associated with a poorer progression-free survival in a univariate analysis. Our result enlightens the accumulation of aberrant DNA methylation which occurs in concordance with the tumor progression.
机译:我们调查了某些microRNA的CpG岛甲基化是​​否与非小细胞肺癌的临床病理特征和预后相关。使用联合的亚硫酸氢盐限制分析法在96个非小细胞肺癌标本中分析了mir-152,-9-3,-124-1,-124-2和-124-3的甲基化。中位观察期为49.5个月。 mir-9-3,-124-2和-124-3的甲基化分别与年龄,性别和吸烟习惯无关的晚期T因子相关。此外,在单变量分析中,多个microRNA基因座的甲基化与较差的无进展生存期相关。我们的结果启发了与肿瘤进展一致的异常DNA甲基化的积累。

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    《Cancer science.》 |2011年第12期|共6页
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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
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