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Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia

机译:WWOX,FHIT和P73在急性淋巴细胞白血病中的基因表达

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摘要

The aim of the present study was to analyze the expression of WW-domain oxidoreductase (WWOX), fragile histidine triad (FHIT) and p73 in acute lymphoblastic leukemia (ALL). Samples from 122 ALL patients and 35 non-ALL control patients were collected in this study. RT-PCR was performed to detect the mRNA expression of WWOX, FHIT and p73. The methylation status of the WWOX promoter region, FHIT promoter region and the first exon region of p73 were also analyzed using the methylation-specific PCR method. The mRNA expression of WWOX, FHIT and p73 was significantly lower in the ALL samples compared with the controls (48.2, 42.9 and 55.4%, respectively). By contrast, the methylation frequency of WWOX, FHIT and p73 was significantly higher in the ALL samples compared with the controls (44.6, 46.4 and 37.5%, respectively). The mRNA expression of these three genes was inversely correlated with the methylation frequency in the ALL samples (correlation coefficients, -0.661, -0.685 and -0.536 for WWOX, FHIT and p73, respectively). Moreover, the mRNA expression of WWOX was positively correlated with that of FHIT and p73 (correlation coefficients, 0.569 and 0.556, respectively). However, the methylation status of WWOX had no correlation with that of FHIT or p73. It was concluded that the high methylation status of WWOX, FHIT and p73 may lead to the inactivation of expression and the silencing of these genes, promoting the occurrence and development of ALL. The determination of the mRNA expression and methylation status of WWOX, FHIT and p73 may aid in the development of treatment approaches for ALL.
机译:本研究的目的是分析急性淋巴细胞白血病(全部)中的WW-结构域氧化还原酶(WWOX),脆弱组氨酸三合会(FHIT)和P73的表达。在这项研究中收集了122名患者和35名非所有对照患者的样品。进行RT-PCR以检测WWOX,FHIT和P73的mRNA表达。还使用甲基化特异性PCR方法分析Wwox启动子区,FHIT启动子区和P73的第一外显子区域的甲基化状态。与对照(48.2,42.9和55.4%)相比,所有样品中WWOX,FHIT和P73的mRNA表达显着降低(48.2,42.9和55.4%)。相比之下,与对照(分别为44.6,46.4和37.5%)相比,所有样品中,WWOX,FHIT和P73的甲基化频率显着较高。这三种基因的mRNA表达与所有样品中的甲基化频率与WWOX,FHIT和P73的所有样品中的甲基化频率与甲基化频率相反。此外,WWOX的mRNA表达与FHIT和P73(分别相关系数,0.569和0.556)呈正相关。然而,WWOX的甲基化状态与FHIT或P73的甲基化状态无关。得出结论是,WWOX,FHIT和P73的高甲基化状态可能导致表达的灭活和这些基因的沉默,促进所有的发生和发展。 WWOX,FHIT和P73的mRNA表达和甲基化状态的测定可以有助于所有的处理方法。

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  • 来源
    《Oncology letters》 |2013年第4期|共7页
  • 作者单位

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

    Department of Clinical Laboratory First Affiliated Hospital of Guangxi Medical University Nanning;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

    Acute lymphoblastic leukemia; FHIT; Methylation; mRNA expression; p73; WWOX;

    机译:急性淋巴细胞白血病;fhit;甲基化;mRNA表达;p73;wwox;

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