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甲基化的凋亡蛋白酶激活因子-1(APAF-1)和死亡相关蛋白激酶-1(DAPK-1)肿瘤抑制基因的信使核糖核酸(mRNA)表达谱揭示了具有侵袭性表型的透明细胞肾细胞癌。

mRNA expression profiles of methylated APAF-1 and DAPK-1 tumor suppressor genes uncover clear cell renal cell carcinomas with aggressive phenotype.

作者信息

Christoph F, Hinz S, Kempkensteffen C, Schostak M, Schrader M, Miller K

机构信息

Department of Urology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

出版信息

J Urol. 2007 Dec;178(6):2655-9. doi: 10.1016/j.juro.2007.07.116. Epub 2007 Oct 22.

Abstract

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 inversely with 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.

摘要

目的

我们确定了55例连续的肿瘤及相应正常组织样本中,p53靶基因APAF-1和DAPK-1的启动子甲基化与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,中位随访时间为75个月。采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聚合酶链反应。

结果

同一肾脏的肿瘤组织与非肿瘤组织相比,APAF-1和DAPK-1的mRNA表达水平显著更高(分别为p = 0.003和0.0001)。这两个基因的表达水平与肿瘤分期无关,但在高级别(G3)肿瘤中显著更低(分别为p = 0.018和0.05)。在淋巴结分期为阳性的患者中,APAF-1和DAPK-1的mRNA表达显著更低。对肿瘤组织进行配对分析时,APAF-1基因的甲基化水平与mRNA表达水平呈负相关(p = 0.02)。在病变4 cm或更大的患者的肿瘤和正常肾组织中,后来发生转移的患者DAPK-1的mRNA表达水平显著更低(分别为p = 0.04和0.02)。

结论

这些数据表明,在侵袭性更强的透明细胞肾细胞癌亚型中,肿瘤抑制基因表达降低。临床结局不佳的患者的肿瘤和正常组织中DAPK-1基因的mRNA水平较低,提示肿瘤抑制基因表达存在器官特异性缺失,易发生转移性肿瘤疾病且总生存期较短。

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