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用于结直肠癌早期检测的血浆SEPT9基因甲基化检测技术进展

Advance in plasma SEPT9 gene methylation assay for colorectal cancer early detection.

作者信息

Wang Yu, Chen Pei-Min, Liu Rong-Bin

机构信息

School of Public Health, Guangzhou Medical University, Guangzhou 510180, Guangdong Province, China.

Department of Ultrasound, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China.

出版信息

World J Gastrointest Oncol. 2018 Jan 15;10(1):15-22. doi: 10.4251/wjgo.v10.i1.15.

DOI:10.4251/wjgo.v10.i1.15
PMID:29375744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5767789/
Abstract

This review article summarizes the research advances of the plasma-based gene methylation assay for the clinical detection of colorectal cancer and its limitations. Colorectal cancer is a common malignancy with a poor prognosis and a high mortality, for which early detection and diagnosis are particularly crucial for the high-risk groups. Increasing evidence supported that gene methylation is associated with the pathogenesis of colorectal cancer and that detecting the level of methylation of in the peripheral blood can be used for screening of colorectal cancer in susceptible populations. In recent years, the data obtained in clinical studies demonstrated that the gene methylation assay has a good diagnostic performance with regard to both sensitivity and specificity with the advantage of better acceptability, convenience and compliance with serological testing compared with fecal occult blood tests and carcinoembryonic antigen for colorectal cancer (CRC). Furthermore, the combination of multiple methods or markers has become a growing trend for CRC detection and screening. Nevertheless, the clinical availability of the methylated SEPT9 assay is still limited because of the large degree of sample heterogeneity caused by demographic characteristics, pathological features, comorbidities and/or technique selection. Another factor is the cost-effectiveness of colorectal cancer screening strategies that hinders its large-scale application. In addition, improvements in its accuracy in detecting adenomas and premalignant polyps are required.

摘要

这篇综述文章总结了基于血浆的基因甲基化检测法在结直肠癌临床检测方面的研究进展及其局限性。结直肠癌是一种常见的恶性肿瘤,预后较差且死亡率高,对于高危人群而言,早期检测和诊断尤为关键。越来越多的证据表明,基因甲基化与结直肠癌的发病机制相关,检测外周血中特定基因的甲基化水平可用于易感人群的结直肠癌筛查。近年来,临床研究获得的数据表明,与结直肠癌(CRC)的粪便潜血试验和癌胚抗原相比,特定基因甲基化检测法在敏感性和特异性方面均具有良好的诊断性能,且具有更好的可接受性、便利性以及与血清学检测的依从性等优势。此外,多种方法或标志物的联合已成为结直肠癌检测和筛查的发展趋势。然而,由于人口统计学特征、病理特征、合并症和/或技术选择导致样本异质性程度较大,甲基化SEPT9检测法的临床实用性仍然有限。另一个因素是结直肠癌筛查策略的成本效益,这阻碍了其大规模应用。此外,还需要提高其在检测腺瘤和癌前息肉方面的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3734/5767789/6e2312fbefbf/WJGO-10-15-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3734/5767789/6e2312fbefbf/WJGO-10-15-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3734/5767789/6e2312fbefbf/WJGO-10-15-g001.jpg

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本文引用的文献

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The performance of the SEPT9 gene methylation assay and a comparison with other CRC screening tests: A meta-analysis.SEPT9 基因甲基化检测的性能及其与其他 CRC 筛查试验的比较:一项荟萃分析。
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Colorectal cancer statistics, 2017.结直肠癌统计数据,2017 年。
通过检测肺活检和淋巴结活检标本中的[具体物质]和[具体物质]甲基化状态提高肺癌辅助诊断的准确性。
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Colorectal Cancer: Risk Factors, Novel Approaches in Molecular Screening and Treatment.结直肠癌:风险因素、分子筛查与治疗的新方法
Int J Mol Cell Med. 2025;14(1):576-605. doi: 10.22088/IJMCM.BUMS.14.1.576.
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SEPT9: From pan-cancer to lung squamous cell carcinoma.SEPT9:从泛癌到肺鳞癌。
BMC Cancer. 2024 Sep 5;24(1):1105. doi: 10.1186/s12885-024-12877-4.
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DNA methylation is associated with breast cancer recurrence or metastasis.DNA 甲基化与乳腺癌的复发或转移有关。
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Circulating tumor DNA for monitoring colorectal cancer: A prospective observational study to assess the presence of methylated SEPT9 and VIM promoter genes and its role as a biomarker in colorectal cancer management.循环肿瘤DNA用于监测结直肠癌:一项前瞻性观察性研究,评估甲基化SEPT9和VIM启动子基因的存在及其作为生物标志物在结直肠癌管理中的作用。
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J Mol Diagn. 2016 Jul;18(4):535-45. doi: 10.1016/j.jmoldx.2016.02.005. Epub 2016 Apr 28.