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用于非侵入性检测结直肠癌的生物标志物:DNA、RNA还是蛋白质?

Biomarkers for detecting colorectal cancer non-invasively: DNA, RNA or proteins?

作者信息

Loktionov Alexandre

机构信息

DiagNodus Ltd, Babraham Research Campus, Cambridge CB22 3AT, United Kingdom.

出版信息

World J Gastrointest Oncol. 2020 Feb 15;12(2):124-148. doi: 10.4251/wjgo.v12.i2.124.

Abstract

Colorectal cancer (CRC) is a global problem affecting millions of people worldwide. This disease is unique because of its slow progress that makes it preventable and often curable. CRC symptoms usually emerge only at advanced stages of the disease, consequently its early detection can be achieved only through active population screening, which markedly reduces mortality due to this cancer. CRC screening tests that employ non-invasively detectable biomarkers are currently being actively developed and, in most cases, samples of either stool or blood are used. However, alternative biological substances that can be collected non-invasively (colorectal mucus, urine, saliva, exhaled air) have now emerged as new sources of diagnostic biomarkers. The main categories of currently explored CRC biomarkers are: (1) Proteins (comprising widely used haemoglobin); (2) DNA (including mutations and methylation markers); (3) RNA (in particular microRNAs); (4) Low molecular weight metabolites (comprising volatile organic compounds) detectable by metabolomic techniques; and (5) Shifts in gut microbiome composition. Numerous tests for early CRC detection employing such non-invasive biomarkers have been proposed and clinically studied. While some of these studies generated promising early results, very few of the proposed tests have been transformed into clinically validated diagnostic/screening techniques. Such DNA-based tests as Food and Drug Administration-approved multitarget stool test (marketed as Cologuard) or blood test for methylated septin 9 (marketed as Epi proColon 2.0 CE) show good diagnostic performance but remain too expensive and technically complex to become effective CRC screening tools. It can be concluded that, despite its deficiencies, the protein (haemoglobin) detection-based faecal immunochemical test (FIT) today presents the most cost-effective option for non-invasive CRC screening. The combination of non-invasive FIT and confirmatory invasive colonoscopy is the current strategy of choice for CRC screening. However, continuing intense research in the area promises the emergence of new superior non-invasive CRC screening tests that will allow the development of improved disease prevention strategies.

摘要

结直肠癌(CRC)是一个全球性问题,影响着全球数百万人。这种疾病具有独特性,因为其进展缓慢,这使得它具有可预防性且通常可治愈。CRC症状通常仅在疾病晚期出现,因此只有通过积极的人群筛查才能实现早期检测,这显著降低了这种癌症导致的死亡率。目前正在积极开发采用非侵入性可检测生物标志物的CRC筛查测试,在大多数情况下,使用粪便或血液样本。然而,现在可以非侵入性收集的替代生物物质(结直肠黏液、尿液、唾液、呼出气体)已成为诊断生物标志物的新来源。目前探索的CRC生物标志物的主要类别包括:(1)蛋白质(包括广泛使用的血红蛋白);(2)DNA(包括突变和甲基化标记);(3)RNA(特别是微小RNA);(4)可通过代谢组学技术检测的低分子量代谢物(包括挥发性有机化合物);以及(5)肠道微生物群组成的变化。已经提出并对许多采用此类非侵入性生物标志物进行早期CRC检测的测试进行了临床研究。虽然其中一些研究产生了有希望的早期结果,但很少有提议的测试转化为经过临床验证的诊断/筛查技术。诸如美国食品药品监督管理局批准的多靶点粪便检测(商品名为Cologuard)或甲基化septin 9血液检测(商品名为Epi proColon 2.0 CE)等基于DNA的测试显示出良好的诊断性能,但仍然过于昂贵且技术复杂,无法成为有效的CRC筛查工具。可以得出结论,尽管存在不足,但基于蛋白质(血红蛋白)检测的粪便免疫化学检测(FIT)目前是无创CRC筛查最具成本效益的选择。无创FIT与确诊性侵入性结肠镜检查相结合是目前CRC筛查的首选策略。然而,该领域持续的深入研究有望出现新的更优质的无创CRC筛查测试,这将有助于制定更好的疾病预防策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7263/7031146/565a1ac9182c/WJGO-12-124-g001.jpg

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