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首页> 外文期刊>Carcinogenesis >Single-CpG-resolution methylome analysis identifies clinicopathologically aggressive CpG island methylator phenotype clear cell renal cell carcinomas
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Single-CpG-resolution methylome analysis identifies clinicopathologically aggressive CpG island methylator phenotype clear cell renal cell carcinomas

机译:单CpG分辨率甲膜分析识别临床病理侵略性CPG岛甲基甲虫表型清除细胞肾细胞癌

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摘要

To clarify the significance of DNA methylation alterations during renal carcinogenesis, methylome analysis using single-CpG-resolution Infinium array was performed on 29 normal renal cortex tissue (C) samples, 107 non-cancerous renal cortex tissue (N) samples obtained from patients with clear cell renal cell carcinomas (RCCs) and 109 tumorous tissue (T) samples. DNA methylation levels at 4830 CpG sites were already altered in N samples compared with C samples. Unsupervised hierarchical clustering analysis based on DNA methylation levels at the 801 CpG sites, where DNA methylation alterations had occurred in N samples and were inherited by and strengthened in T samples, clustered clear cell RCCs into Cluster A (n = 90) and Cluster B (n = 14). Clinicopathologically aggressive tumors were accumulated in Cluster B, and the cancer-free and overall survival rates of patients in this cluster were significantly lower than those of patients in Cluster A. Clear cell RCCs in Cluster B were characterized by accumulation of DNA hypermethylation on CpG islands and considered to be CpG island methylator phenotype (CIMP)-positive cancers. DNA hypermethylation of the CpG sites on the FAM150A, GRM6, ZNF540, ZFP42, ZNF154, RIMS4, PCDHAC1, KHDRBS2, ASCL2, KCNQ1, PRAC, WNT3A, TRH, FAM78A, ZNF671, SLC13A5 and NKX6-2 genes became hallmarks of CIMP in RCCs. On the other hand, Cluster A was characterized by genome-wide DNA hypomethylation. These data indicated that DNA methylation alterations at precancerous stages may determine tumor aggressiveness and patient outcome. Accumulation of DNA hypermethylation on CpG islands and genome-wide DNA hypomethylation may each underlie distinct pathways of renal carcinogenesis. Abbreviations: BAMCAbacterial artificial chromosome array-based methylated CpG island amplification. Cnormal renal cortex tissue obtained from patients without any primary renal tumor. CIMPCpG island methylator phenotype. HCChepatocellular carcinoma. Nnon-cancerous renal cortex tissue obtained from patients with clear cell renal cell carcinomas. NCBINational Center for Biotechnology Information. RCCrenal cell carcinoma. Ttumorous tissue. TNMTumor-Node-Metastasis.
机译:为了澄清DNA致癌过程中DNA甲基化改变的重要性,在29例正常肾皮层组织(C)样品上进行使用单CpG分辨率infinium阵列的甲基族分析,107个非癌性肾皮质组织(n)样品透明细胞肾细胞癌(RCC)和109个肿瘤组织(T)样品。与C样品相比,在N样品中已经改变了4830个CPG位点的DNA甲基化水平。在801个CPG位点的DNA甲基化水平的无监督分层聚类分析,其中在N个样品中发生DNA甲基化改变,并在T样品中遗传并加强,聚类透明细胞RCC成簇A(n = 90)和簇B( n = 14)。临床病理侵袭性肿瘤累积在B组中,该簇中患者的无癌症和整体存活率显着低于簇A中的患者。群体B中的透明细胞RCCS通过CPG岛上的DNA高甲基化积累的特征是表征并被认为是CpG岛甲基甲蛋白表型(CIMP) - 阳性癌症。 DNA在FAM150A,GRM6,ZNF540,ZFP42,ZNF154,RIMS4,PCDHAC1,KHDRBS2,ASCL2,KCNQ1,PRAC,WNT3A,TRH,FAM78A,ZNF671,SLC13A5和NKX6-2基因上的DNA高甲基化物质的DNA高甲基化的DNA高甲基化位于ZFP42,ZNF154,ASCL2,KCNQ1,PRAC,WNT3A,SLC13A5和NKX6-2基因成为CIMP的标志。另一方面,簇A的特征在于宽的基因组DNA低甲基化。这些数据表明,癌前阶段的DNA甲基化改变可以确定肿瘤侵袭性和患者结果。 DNA高甲基化对CPG岛和基因组的DNA低甲基化的积累可以各自为肾癌发生的底层明显的途径。缩写:基于Bamcabacterial人工染色体阵列的甲基化CpG岛扩增。没有任何原发性肾肿瘤的患者获得的CNORAL肾皮层组织。 Cimpcpg岛甲基素表型。 Hcchepatocellular癌。 NNON-癌性肾皮质组织从透明细胞肾细胞癌患者获得。生物技术信息的NcBinational。 rccrenal细胞癌。 T.rumory组织。 tnmtumor-node-metastasis。

著录项

  • 来源
    《Carcinogenesis 》 |2012年第8期| 共7页
  • 作者单位

    Division of Molecular Pathology National Cancer Center Research Institute Tokyo 104-0045 Japan;

    Science Solutions Division Mizuho Information and Research Institute Inc. Tokyo 101-8443 Japan;

    Division of Molecular Pathology National Cancer Center Research Institute Tokyo 104-0045 Japan;

    Division of Molecular Pathology National Cancer Center Research Institute Tokyo 104-0045 Japan;

    Department of Urology National Cancer Center Hospital Tokyo 104-0045 Japan;

    Department of Urology National Cancer Center Hospital Tokyo 104-0045 Japan;

    Division of Molecular Pathology National Cancer Center Research Institute Tokyo 104-0045 Japan;

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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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