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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Coordinated Cancer Germline Antigen Promoter and Global DNA Hypomethylation in Ovarian Cancer: Association with the BORIS/CTCF Expression Ratio and Advanced Stage.
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Coordinated Cancer Germline Antigen Promoter and Global DNA Hypomethylation in Ovarian Cancer: Association with the BORIS/CTCF Expression Ratio and Advanced Stage.

机译:卵巢癌中协调一致的癌症生殖细胞抗原启动子和整体DNA甲基化不足:与BORIS / CTCF表达比和晚期相关。

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PURPOSE: Cancer germline (CG) antigens are frequently expressed and hypomethylated in epithelial ovarian cancer (EOC), but the relationship of this phenomenon to global DNA hypomethylation is unknown. In addition, the potential mechanisms leading to DNA hypomethylation, and its clinicopathologic significance in EOC, have not been determined. EXPERIMENTAL DESIGN: We used quantitative mRNA expression and DNA methylation analyses to determine the relationship between expression and methylation of X-linked (MAGE-A1, NY-ESO-1, XAGE-1) and autosomal (BORIS, SOHLH2) CG genes, global DNA methylation (5mdC levels, LINE-1, Alu, and Sat-alpha methylation), and clinicopathology, using 75 EOC samples. In addition, we examined the association between these parameters and a number of mechanisms proposed to contribute to DNA hypomethylation in cancer. RESULTS: CG genes were coordinately expressed in EOC and this was associated with promoter DNA hypomethylation. Hypomethylation of CG promoters was highly correlated and strongly associated with LINE-1 and Alu methylation, moderately with 5mdC levels, and rarely with Sat-alpha methylation. BORIS and LINE-1 hypomethylation, and BORIS expression, were associated with advanced stage. GADD45A expression, MTHFR genotype, DNMT3B isoform expression, and BORIS mRNA expression did not associate with methylation parameters. In contrast, the BORIS/CTCF expression ratio was associated with DNA hypomethylation, and furthermore correlated with advanced stage and decreased survival. CONCLUSIONS: DNA hypomethylation coordinately affects CG antigen gene promoters and specific repetitive DNA elements in EOC, and correlates with advanced stage disease. The BORIS/CTCF mRNA expression ratio is closely associated with DNA hypomethylation and confers poor prognosis in EOC. Clin Cancer Res; 17(8); 2170-80. (c)2011 AACR.
机译:目的:癌种系(CG)抗原在上皮性卵巢癌(EOC)中经常表达和甲基化不足,但是这种现象与总体DNA甲基化不足的关系尚不清楚。此外,尚未确定导致DNA低甲基化的潜在机制及其在EOC中的临床病理意义。实验设计:我们使用定量的mRNA表达和DNA甲基化分析来确定X连锁(MAGE-A1,NY-ESO-1,XAGE-1)和常染色体(BORIS,SOHLH2)CG基因的表达与甲基化之间的关系使用75个EOC样本进行DNA甲基化(5mdC水平,LINE-1,Alu和Sat-α甲基化)和临床病理。此外,我们检查了这些参数与许多机制之间的关联,这些机制被认为有助于癌症中的DNA低甲基化。结果:CG基因在EOC中协同表达,这与启动子DNA低甲基化有关。 CG启动子的低甲基化与LINE-1和Alu甲基化高度相关且高度相关,与5mdC水平适度相关,而与Sat-α甲基化很少相关。 BORIS和LINE-1的低甲基化以及BORIS的表达与晚期有关。 GADD45A表达,MTHFR基因型,DNMT3B亚型表达和BORIS mRNA表达与甲基化参数无关。相比之下,BORIS / CTCF表达比率与DNA低甲基化有关,并且还与晚期阶段和存活率降低有关。结论:DNA低甲基化协调影响EOC中的CG抗原基因启动子和特定的重复性DNA元素,并与晚期疾病相关。 BORIS / CTCF mRNA表达比率与DNA低甲基化密切相关,并赋予EOC预后不良。临床癌症研究; 17(8); 2170-80。 (c)2011年美国机修协会。

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