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Overexpression of the MUC2 gene through promoter hypomethylation in mucinous cell carcinomas and signet ring cell carcinomas of gastric cancer

机译:MUC2基因通过启动子低甲基化在胃黏液细胞癌和印戒细胞癌中的过表达

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摘要

Gastric carcinoma (GC) remains an important cause of mortality and morbidity in East Asia and the histological classification is still controversial, despite considerable understanding of the molecular nature of this disease and its precursor lesions.Mucins play important roles in carcinogenesis or tumor invasion and their aberrant expression are also associated with pathophysiological conditions and clinical outcomes. To investigate if differences with MUC2 expression in GC are associated through changes in promoter methylation and to evaluate the relationship with the histological features of GCs, the expression and methylation status of MUC2 gene was examined in samples from 40 gastric mucosa of GC by immunohistochemistry (IHC) and by methylation-specific PCR (MSP). MUC2 was minimally and focally expressed in well-differentiated (WD) and moderately-differentiated (MD) GC, while mucinous cell carcinomas (MCC) and signet ring cell carcinomas (SRC) displayed a uniform and strong staining intensitywith a diffused cytoplasmic pattern. In addition, the MUC2 hypomethylation were found in 33% of the WD, 0% of the MD, 77% of the MCC, 75% of the MCC/SRC, and 80% of the SRC. Moreover, IHC and MSP analyses showed that MUC2 hypomethylation correlated withits overexpression. Collectively, these results suggest that MUC2 overexpression mediated by promoter hypomethylation may be a common event in MCC and SRC types of GCs. However, further studies with large numbers of patients will be needed to confirm these findings.
机译:胃癌(GC)仍然是东亚地区死亡率和发病率的重要原因,尽管对这种疾病及其前体病变的分子性质有相当的了解,但组织学分类仍存在争议。粘蛋白在致癌或肿瘤侵袭及其发生中起着重要作用。异常表达还与病理生理状况和临床结果相关。为研究是否通过启动子甲基化的变化与GC中MUC2表达的差异有关并评估其与GCs的组织学特征之间的关系,采用免疫组织化学方法(IHC)检测了40个胃癌胃黏膜样品中MUC2基因的表达和甲基化状态)并通过甲基化特异性PCR(MSP)。 MUC2在高分化(WD)和中分化(MD)GC中极少且集中表达,而粘液细胞癌(MCC)和印戒细胞癌(SRC)表现出均匀而强的染色强度,具有弥散的细胞质模式。另外,在33%的WD,0%的MD,77%的MCC,75%的MCC / SRC和80%的SRC中发现了MUC2的低甲基化。此外,IHC和MSP分析表明MUC2的甲基化不足与其过表达有关。总的来说,这些结果表明由启动子低甲基化介导的MUC2过表达可能是MCC和SRC类型的GC中的常见事件。但是,将需要对大量患者进行进一步研究以证实这些发现。

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