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首页> 外文期刊>Oncology letters >Promoter methylation and downregulated expression of the TBX15 gene in ovarian carcinoma
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Promoter methylation and downregulated expression of the TBX15 gene in ovarian carcinoma

机译:TBX15基因在卵巢癌中的启动子甲基化和下调表达

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摘要

TBX15 is a gene involved in the development of mesodermal derivatives. As the ovaries and the female reproductive system are of mesodermal origin, the aim of the present study was to determine the methylation status of the TBX15 gene promoter and the expression levels of TBX15 in ovarian carcinoma, which is the most lethal and aggressive type of gynecological tumor, in order to determine the role of TBX15 in the pathogenesis of ovarian carcinoma. This alteration could be used to predict tumor development, progression, recurrence and therapeutic effects. The study was conducted on 80 epithelial ovarian carcinoma and 17 control cases (normal ovarian and tubal tissues). TBX15 promoter methylation was first determined by pyrosequencing following bisulfite modification, then by cloning and sequencing, in order to obtain information about the epigenetic haplotype. Immunohistochemical analysis was performed to evaluate the correlation between the methylation and protein expression levels. Data revealed a statistically significant increase of the TBX15 promoter region methylation in 82% of the tumor samples and in various histological subtypes. Immunohistochemistry showed an inverse correlation between methylation levels and the expression of the TBX15 protein. Furthermore, numerous tumor samples displayed varying degrees of intratumor heterogeneity. Thus, the present study determined that ovarian carcinoma typically expresses low levels of TBX15 protein, predominantly due to an epigenetic mechanism. This may have a role in the pathogenesis of ovarian carcinoma independent of the histological subtype.
机译:TBX15是参与中胚层衍生物开发的基因。由于卵巢和女性生殖系统是中胚层来源的,因此本研究的目的是确定TBX15基因启动子的甲基化状态以及TBX15在卵巢癌中的表达水平,这是最致命,最积极的妇科类型。为了确定TBX15在卵巢癌的发病机理中的作用,这种改变可用于预测肿瘤的发展,进展,复发和治疗效果。该研究针对80例上皮性卵巢癌和17例对照病例(正常的卵巢和输卵管组织)进行。首先通过亚硫酸氢盐修饰后的焦磷酸测序来确定TBX15启动子的甲基化,然后通过克隆和测序来确定有关表观遗传单倍型的信息。进行了免疫组织化学分析以评估甲基化和蛋白质表达水平之间的相关性。数据显示在82%的肿瘤样品和各种组织学亚型中TBX15启动子区域甲基化在统计学上显着增加。免疫组织化学显示甲基化水平与TBX15蛋白表达呈负相关。此外,许多肿瘤样品显示出不同程度的肿瘤内异质性。因此,本研究确定卵巢癌通常表达低水平的TBX15蛋白,这主要归因于表观遗传机制。这可能在卵巢癌的发病机理中具有独立于组织学亚型的作用。

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