数字聚合酶链反应
循环肿瘤DNA
微小残留病
癌症
DNA测序
液体活检
医学
循环肿瘤细胞
肿瘤科
癌症生物标志物
表观遗传学
内科学
癌症的体细胞进化
计算生物学
聚合酶链反应
癌症研究
DNA
生物
基因
遗传学
白血病
转移
作者
Mathilde Postel,Alice Roosen,Pierre Laurent‐Puig,Valérie Taly,Shufang Renault
标识
DOI:10.1080/14737159.2018.1400384
摘要
Introduction: Early detection of cancers through the analysis of ctDNA could have a significant impact on morbidity and mortality of cancer patients. However, using ctDNA for early cancer diagnosis is challenging partly due to the low amount of tumor DNA released in the circulation and its dilution within DNA originating from non-tumor cells. Development of new technologies such as droplet-based digital PCR (ddPCR) or optimized next generation sequencing (NGS) has greatly improved the sensitivity, specificity and precision for the detection of rare sequences.Areas covered: This paper will focus on the potential application of ddPCR and optimized NGS to detect ctDNA for detection of cancer recurrence and minimal residual disease as well as early diagnosis of cancer patients.Expert commentary: Compared to tumor tissue biopsies, blood-based ctDNA analyses are minimally invasive and accessible for regular follow-up of cancer patients. They are also described as a better picture of patients' pathology allowing to highlight both tumor heterogeneity and multiple tumor sites. After a brief introduction on the application of the follow-up of ctDNA using genetic or epigenetic biomarkers for prognosis and surveillance of cancer patients, potential perspectives of using ctDNA for early diagnosis of cancers will be presented.
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