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Detection of aberrant methylated SEPT9 and NTRK3 genes in sporadic colorectal cancer patients as a potential diagnostic biomarker

机译:检测散发性结直肠癌患者中异常甲基化的SEPT9和NTRK3基因可作为潜在的诊断生物标志物

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摘要

Colorectal cancer (CRC) is one of the most common malignancies, and the third leading cause of cancer mortality worldwide. Timely detection of CRC in patients with earlier stages provides the highest rate of survival. Epigenetic alterations are important in the occurrence and progression of CRC, and represent the primary modifications of cancer cells. Therefore, detection of these alterations in CRC cases are thought to hold great promise as diagnostic biomarkers. It has been shown that the SEPT9 and NTRK3 genes are aberrantly methylated and their detection can be used as biomarkers for early diagnosis of CRC. The present study analyzed promoter methylation status of these genes in CRC patients. Genomic DNA was extracted from 45 CRC and paired adjacent healthy tissues and undergone bisulfite conversion, and the methylation status of NTRK3 and SEPT9 were defined using the MS-HRM assay. Our results showed that there are statistically significant differences in methylation status of NTRK3 and specially SEPT9 between CRC and adjacent normal tissues (P<0.001). High sensitivity and specificity for a specific location in SEPT9 gene promoter as a diagnostic biomarker was observed. SEPT9 promoter hypermethylation may serve as a promising biomarker for the detection of CRC development. However, to validate the biomarker potential of NTRK3 there is a requirement for further investigation.
机译:大肠癌(CRC)是最常见的恶性肿瘤之一,也是全球癌症死亡的第三大主要原因。在早期阶段的患者中及时发现CRC可提供最高的存活率。表观遗传改变在CRC的发生和发展中很重要,并且代表了癌细胞的主要修饰。因此,在CRC病例中检测这些改变被认为具有作为诊断生物标志物的巨大希望。已显示SEPT9和NTRK3基因异常甲基化,它们的检测可用作早期CRC诊断的生物标记。本研究分析了CRC患者中这些基因的启动子甲基化状态。从45个CRC中提取基因组DNA,并将其配对到相邻的健康组织中并进行亚硫酸氢盐转化,并使用MS-HRM分析确定NTRK3和SEPT9的甲基化状态。我们的结果表明,在CRC和邻近正常组织之间,NTRK3尤其是SEPT9的甲基化状态存在统计学差异(P <0.001)。观察到作为诊断生物标志物的SEPT9基因启动子中特定位置的高灵敏度和特异性。 SEPT9启动子的甲基化水平高,可作为检测CRC发育的有前途的生物标记。然而,为了验证NTRK3的生物标志物潜力,需要进一步研究。

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