>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
血浆中ZNF582甲基化在结直肠癌早期诊断中的可行性研究
作者:戴彦苗  彭惠平  王杰  夏晨静  高黎明  徐宏伟 
单位:昆山市中医医院 脾胃肝胆科, 江苏 昆山 215300
关键词:结直肠癌 甲基化 血浆 ZNF582 诊断 
分类号:R735.3
出版年·卷·期(页码):2023·42·第二期(252-256)
摘要:

目的:探讨血浆锌指蛋白582(zinc finger protein 582, ZNF582)基因甲基化检测用于结直肠癌早期诊断的可行性。方法: 选择2021年1月至2022年6月在昆山市中医医院就诊的结直肠癌患者78例(直肠癌组)、结直肠息肉患者62例(结直肠息肉组)为研究对象,另选83例结肠镜检查正常者作为正常对照组。采用甲基化特异性荧光定量PCR检测血浆中ZNF582的甲基化状态,并进行统计学分析。 结果: ZNF582在结直肠癌组患者血浆中的甲基化水平显著高于结直肠息肉组和正常对照组(P<0.000 1)。ROC曲线分析显示,ZNF582甲基化用于诊断结直肠癌的AUC为0.879(95%CI 0.818~0.925)。ZNF582甲基化对结直肠息肉和结直肠癌的检测灵敏度分别为37.1%、73.1%,对结直肠病变的诊断特异性为90.4%。ZNF582甲基化对不同性别、分期、分化程度以及肿瘤大小的结直肠癌检测灵敏度无显著差异。结论:血浆ZNF582可以作为一种潜在的操作简便的、非侵入性结直肠癌早期诊断替代方案。

Objective: To investigate the feasibility of plasma-based methylated zinc finger protein 582(ZNF582) for early detection of colorectal cancer. Methods: From January 2021 to June 2022, the plasma of 78 colorectal cancers(colorectal cancer group), 62 colorectal polyps(colorectal polyp group)and 83 normal control subjects(control group) in Kunshan Hospital of Traditional Chinese Medicine were collected. The methylation levels of ZNF582 in plasma was detected by methylation-specific fluorescence quantitative PCR, and statistical analysis was performed. Results: The methylation level of ZNF582 in plasma of colorectal cancer group was significantly higher than that in colorectal polyp group and control group(P<0.000 1). The AUC of methylated ZNF582 methylation for detection of colorectal cancer was 0.879(95% CI 0.818-0.925). The sensitivities of methylated ZNF582 for detecting colorectal polyps and colorectal cancer were 37.1% and 73.1%, respectively, and the specificity of colorectal disease was 90.4%. Methylated ZNF582 had no significant difference in the detection of colorectal cancer with different gender, stage, differentiation and tumor size. Conclusion: Plasma-based methylated ZNF582 can be used as a potential non-invasive alternative for early diagnosis of colorectal cancer.

参考文献:

[1] ZHENG R,ZHANG S,ZENG H,et al.Cancer incidence and mortality in China,2016[J].J Natl Cancer Cent,2022,2(1):1-9.
[2] LICHTENSTERN C R,NGU R K,SHALAPOUR S,et al.Immunotherapy,inflammation and colorectal cancer[J].Cells,2020,9(3):618.
[3] ZENG H,RAN X,AN L,et al.Disparities in stage at diagnosis for five common cancers in China:a multicentre,hospital-based,observational study[J].Lancet Public Health,2021,6(12):e877-e887.
[4] LIU Y,ZHAO G,MIAO J,et al.Performance comparison between plasma and stool methylated SEPT9 tests for detecting colorectal cancer[J].Front Genet,2020,6(11):324.
[5] 翟爱军,杜丽娜,张续乾,等.亚太结直肠癌筛查评分系统在我国体检人群结直肠癌机会性筛查中的应用[J].中华胃肠内镜电子杂志,2018,5(3):114-117.
[6] 张丽丽,李文彬,阮戈冲,等.亚太地区结直肠筛选评分系统在健康体格检查人群结直肠癌筛查中的评价分析[C].重庆:第十四届全国消化系病学术会议,2014:104.
[7] WOLF A M D,FONTHAM E T H,CHURCH T R,et al.Colorectal cancer screening for average-risk adults:2018 guideline update from the American Cancer Society[J].Ca-Cancer J Clin,2018,68(4):250-281.
[8] 陈万青,李霓,兰平.中国结直肠癌筛查与早诊早治指南(2020,北京)[J].中国肿瘤,2021,30(1):1-28.
[9] 高官壮,韩野,匡玉庭.ZNF582基因启动子区在结直肠癌组织中的甲基化状态及临床意义[J].江苏医药,2021,47(1):25-28.
[10] TANG L,LIOU Y L,WAN Z R,et al.Aberrant DNA methylation of PAX1,SOX1 and ZNF582 genes as potential biomarkers for esophageal squamous cell carcinoma[J].Biomed Pharmacother,2019,120:109488.
[11] ZHANG C,FU S,WANG L,et al.The value and clinical significance of ZNF582 gene methylation in the diagnosis of cervical cancer[J].Onco Targets Ther,2021,14:403-411.
[12] CAO Y,ZHAO G,CAO Y,et al.Feasibility of methylated CLIP4 in stool for early detection of colorectal cancer:a training study in Chinese population[J].Front Oncol,2021,11:647066.
[13] NASSAR F J,MSHEIK Z S,NASR R R,et al.Methylated circulating tumor DNA as a biomarker for colorectal cancer diagnosis,prognosis,and prediction[J].Clin Epigenetics,2021,13(1):111.
[14] POTTER N T,HURBAN P,WHITE M N,et al.Validation of a real-time PCR-based qualitative assay for the detection of methylated SEPT9 DNA in human plasma[J].Clin Chem,2014,60(9):1183-1191.
[15] WU D,ZHOU G,JIN P,et al.Detection of colorectal cancer using a simplified SEPT9 gene methylation assay is a reliable method for opportunistic screening[J].J Mole Diagn,2016,18(4):535-545.
[16] WANG J,LIU S,WANG H,et al.Robust performance of a novel stool DNA test of methylated SDC2 for colorectal cancer detection:a multicenter clinical study[J].Clin Epigenetics,2020,12(1):162.
[17] ZHANG D,WANG Y,HU X.Identification and comprehensive validation of a DNA methylation-driven gene-based prognostic model for clear cell renal cell carcinoma[J].DNA Cell Biol,2020,39(10):1799-1812.
[18] LI N,HE Y,MI P,et al.ZNF582 methylation as a potential biomarker to predict cervical intraepithelial neoplasia type Ⅲ/worse:a meta-analysis of related studies in Chinese population[J].Medicine,2019,98(6):e14297.

服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 413481 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364