首页> 外文期刊>The Journal of Urology >mRNA expression profiles of methylated APAF-1 and DAPK-1 tumor suppressor genes uncover clear cell renal cell carcinomas with aggressive phenotype.
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mRNA expression profiles of methylated APAF-1 and DAPK-1 tumor suppressor genes uncover clear cell renal cell carcinomas with aggressive phenotype.

机译:甲基化的APAF-1和DAPK-1肿瘤抑制基因的mRNA表达谱揭示了具有侵袭性表型的透明细胞肾细胞癌。

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PURPOSE: We determined the relation between promoter methylation and mRNA expression of the p53 target genes APAF-1 and DAPK-1 in 55 consecutive tumor and corresponding normal tissue samples. MATERIALS AND METHODS: Tissue was taken from nonmetastatic clear cell renal cell carcinoma at a median followup of 75 months. Quantitative methylation specific real-time polymerase chain reaction and quantitative real-time reverse transcriptase-polymerase chain reaction were used. RESULTS: The mRNA expression levels of APAF-1 and DAPK-1 were significantly higher in tumor vs nontumor tissue from the same kidney (p = 0.003 and 0.0001, respectively). Expression levels of the 2 genes did not correlate with tumor stage but they were significantly lower in high grade (G3) tumors (p = 0.018 and 0.05, respectively). In patients with positive lymph node staging mRNA expression of APAF-1 and DAPK-1 was significantly lower. On matched pair analysis of tumor tissue the methylation level of the APAF-1 gene correlated inverselywith the mRNA expression level (p = 0.02). In tumor and normal kidney tissue from patients with lesions 4 cm or greater mRNA expression levels of DAPK-1 were significantly lower in those who later had metastatic disease (p = 0.04 and 0.02, respectively). CONCLUSIONS: These data demonstrate decreased tumor suppressor gene expression in more aggressive subtypes of clear cell renal cell carcinoma. The lower mRNA level of the DAPK-1 gene in tumor and normal tissue from patients with an unfavorable clinical outcome suggests the organ specific loss of tumor suppressor gene expression, predisposing to metastatic tumor disease and shorter overall survival.
机译:目的:我们确定了55个连续肿瘤和相应的正常组织样本中启动子甲基化与p53靶基因APAF-1和DAPK-1的mRNA表达之间的关系。材料与方法:组织取自非转移性透明细胞肾细胞癌,平均随访75个月。使用定量甲基化特异性实时聚合酶链反应和定量实时逆转录酶-聚合酶链反应。结果:同一肾脏的肿瘤组织中,APAF-1和DAPK-1的mRNA表达水平明显高于非肿瘤组织(分别为p = 0.003和0.0001)。这两种基因的表达水平与肿瘤分期无关,但在高级别(G3)肿瘤中却显着降低(分别为p = 0.018和0.05)。在具有阳性淋巴结分期的患者中,APAF-1和DAPK-1的mRNA表达显着降低。在对肿瘤组织进行配对分析后,APAF-1基因的甲基化水平与mRNA表达水平呈负相关(p = 0.02)。在患有转移性疾病的患者中,具有4 cm或更大病变的患者的肿瘤和正常肾脏组织中DAPK-1的mRNA表达水平显着降低(分别为p = 0.04和0.02)。结论:这些数据证明在透明细胞肾细胞癌的更具侵略性的亚型中,肿瘤抑制基因的表达降低。临床结果不利的患者,肿瘤和正常组织中DAPK-1基因的mRNA水平较低,提示器官特异性肿瘤抑制基因表达的丧失,易导致转移性肿瘤疾病和较短的总生存期。

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