溃疡性结肠炎患者白细胞介素-6异常表达与基因甲基化的关系

Qian Li, Rui Zhang, Jingwen Zhao, Wen-tian Liu
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引用次数: 1

摘要

目的探讨溃疡性结肠炎(UC)患者白细胞介素6 (IL-6)异常表达与基因甲基化的关系,并阐明UC的表观遗传学机制。方法选取2017年3月至2018年3月天津医科大学附属总医院消化内科收治的UC患者59例,同时选取接受健康体检的正常人58例作为健康对照。采集UC组和健康对照组的血液和结肠黏膜标本。检测DNA甲基转移酶(DNMT)活性、IL-6启动子区CpG位点甲基化水平及IL-6表达水平。采用卡方检验和学生t检验进行统计学分析。结果UC组分别有24例和30例完成了甲基化水平和IL-6表达水平检测;健康对照组分别检出21例和20例。UC组DNMT活性显著低于健康对照组((16.48±6.17)OD·h-1·mg-1 vs(62.48±33.88)OD·h-1·mg-1),差异有统计学意义(t=3.707, P<0.05)。UC组的甲基化、部分甲基化、非甲基化率分别为31.2%(15/48)、50.0%(24/48)、18.8%(9/48),健康对照组的甲基化率分别为58.3%(35/60)、21.7%(13/60)、20.0%(12/60),两组差异有统计学意义(χ2=10.495, P<0.05)。UC组IL-6在肠道黏膜的阳性表达率高于健康对照组(100.0%,21/21比25.0%,5/20),差异有统计学意义(χ2=24.837, P<0.05)。UC组血清IL-6水平高于健康对照组((1 075.02±661.95)ng/L vs(583.43±425.10)ng/L),差异有统计学意义(t=3.245, P<0.05)。结论UC患者肠黏膜DNMT活性降低可能降低IL-6基因启动子区甲基化水平,这与肠道黏膜和血清IL-6表达水平升高有关,参与UC的炎症过程。关键词:结肠炎;溃疡性;DNA甲基化;甲基转移酶;白细胞介素- 6
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationship between aberrant expression of interleukin-6 and gene methylation in ulcerative colitis
Objective To investigate the relationship between aberrant expression of interleukin 6 (IL-6) and gene methylation in patients with ulcerative colitis (UC), and to clarify the mechanism of epigenetics in UC. Methods From March 2017 to March 2018, a total of 59 UC patients admitted to the Department of Gastroenterology, General Hospital Affiliated to Tianjin Medical University were enrolled, and at the same time 58 normal individuals who received health checkups were selected as healthy controls. Blood samples and colonic mucosa specimens of UC group and healthy control group were collected. DNA methyltransferase (DNMT) activity, methylation level of CpG locus in IL-6 promoter region and expression level of IL-6 were detected. Chi-square test and student′s t test were performed for statistical analysis. Results The methylation level and IL-6 expression level examination were completed in 24 and 30 cases of UC group, respectively; which were detected in 21 and 20 cases of healthy control group, respectively. The activity of DNMT of UC group was significantly lower than that of healthy control group ((16.48±6.17) OD·h-1·mg-1 vs. (62.48±33.88) OD·h-1·mg-1), and the difference was statistically significant (t=3.707, P<0.05). The ratios of methylation, partial methylation and non-methylation of UC group were 31.2% (15/48), 50.0% (24/48) and 18.8% (9/48), respectively, and those of healthy control group were 58.3%(35/60), 21.7%(13/60) and 20.0%(12/60), and the difference between the two groups was statistically significant (χ2=10.495, P<0.05). The positive expression rate of IL-6 in intestinal mucosa of UC group was higher than that of healthy control group (100.0%, 21/21 vs. 25.0%, 5/20), and the difference was statistically significant (χ2=24.837, P<0.05). The serum IL-6 level of UC group was higher than that of healthy control group ((1 075.02±661.95) ng/L vs. (583.43±425.10) ng/L), and the difference was statistically significant (t=3.245, P<0.05). Conclusion The decrease of DNMT activity in the intestinal mucosa of UC patients may reduce the methylation level of IL-6 gene promoter region, which is correlated with the increased level of IL-6 expression in the intestinal mucosa and serum, and involve in the inflammatory process of UC. Key words: Colitis, ulcerative; DNA methylation; Methyltransferases; Interleukin-6
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