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KDM1A启动子低甲基化与中国汉族人群结直肠癌之间存在显著关联。

Significant association between KDM1A promoter hypomethylation and colorectal cancer in Han Chinese.

作者信息

Zhong Jie, Pan Ranran, Ying Xiuru, Wu Boyi, Zhou Cong, Wu Dongping, Ying Jieer, Duan Shiwei

机构信息

Medical Genetics Center, School of Medicine, Ningbo University, Ningbo, Zhejiang, 315211, China.

Department of Medical Oncology, Shaoxing People's Hospital, Shaoxing Hospital of Zhejiang University, Zhejiang, 312000, China.

出版信息

Pathol Res Pract. 2019 Mar;215(3):532-538. doi: 10.1016/j.prp.2018.12.005. Epub 2018 Dec 7.

Abstract

Lysine-specific histone demethylase 1A gene (KDM1A) promotes tumorigenesis. The aim of this study was to investigate the association between KDM1A methylation and colorectal cancer (CRC). Currently, we collected 37 paired CRC tissues and adjacent non-tumor tissues from Jiangsu province and 75 paired CRC tissues and adjacent non-tumor tissues from Zhejiang province to conduct a two-stage experiment to study the association between KDM1A methylation and CRC. We used qMSP to measure the KDM1A promoter methylation, and the percentage of methylation reference (PMR) to quantify the KDM1A promoter methylation level. To investigate the effect of the selected KDM1A fragment on gene expression regulation, we also performed a dual luciferase reporter gene assay. In the stage I study, the KDM1A promoter methylation level in CRC tumor tissues was significantly lower than that in adjacent non-tumor tissues (median PMR: 6.93% vs 10.25%, P =  0.033). The results of the stage II study were similar to those of the stage I study (mean PMR: 12.94% versus 17.42%, P =  0.016). In addition, a clinical pathology subgroup analysis found that KDM1A hypomethylation was associated with CRC only in patients with well-differentiated CRC (stage I: P =  0.047; stage II: P =  0.040). The dual luciferase reporter assay showed that the transcriptional activity of the recombinant pGL3-KDM1A plasmid was significantly higher (fold change = 2, P =  0.0009). In conclusion, our results suggest that KDM1A hypomethylation is significantly associated with CRC.

摘要

赖氨酸特异性组蛋白去甲基化酶1A基因(KDM1A)促进肿瘤发生。本研究旨在探讨KDM1A甲基化与结直肠癌(CRC)之间的关联。目前,我们收集了来自江苏省的37对结直肠癌组织及相邻非肿瘤组织,以及来自浙江省的75对结直肠癌组织及相邻非肿瘤组织,进行两阶段实验以研究KDM1A甲基化与结直肠癌之间的关联。我们使用qMSP检测KDM1A启动子甲基化,并使用甲基化参考百分比(PMR)来量化KDM1A启动子甲基化水平。为了研究所选KDM1A片段对基因表达调控的影响,我们还进行了双荧光素酶报告基因检测。在第一阶段研究中,结直肠癌肿瘤组织中KDM1A启动子甲基化水平显著低于相邻非肿瘤组织(中位PMR:6.93%对10.25%,P = 0.033)。第二阶段研究结果与第一阶段研究相似(平均PMR:12.94%对17.42%,P = 0.016)。此外,临床病理亚组分析发现,KDM1A低甲基化仅在高分化结直肠癌患者中与结直肠癌相关(I期:P = 0.047;II期:P = 0.040)。双荧光素酶报告检测显示重组pGL3 - KDM1A质粒的转录活性显著更高(倍数变化 = 2,P = 0.0009)。总之,我们的结果表明KDM1A低甲基化与结直肠癌显著相关。

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