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尽管游离DNA存在片段化模式偏差,但它仍能很好地反映肿瘤基因组。

Cell-Free DNA Provides a Good Representation of the Tumor Genome Despite Its Biased Fragmentation Patterns.

作者信息

Ma Xiangyuan, Zhu Liangjun, Wu Xue, Bao Hua, Wang Xiaonan, Chang Zhili, Shao Yang W, Wang Zhenxin

机构信息

Geneseeq Technology Inc., Suite 300, MaRS Centre, South Tower, Toronto, Ontario, Canada.

Jiangsu Cancer Hospital, 42 Baiziting, Xuanwu, Nanjing, Jiangsu, China.

出版信息

PLoS One. 2017 Jan 3;12(1):e0169231. doi: 10.1371/journal.pone.0169231. eCollection 2017.

Abstract

Cell-free DNA (cfDNA) is short, extracellular, fragmented double-stranded DNA found in plasma. Plasma of patients with solid tumor has been found to show significantly increased quantities of cfDNA. Although currently poorly understood, the mechanism of cfDNA generation is speculated to be a product of genomic DNA fragmentation during cellular apoptosis and necrosis. Sequencing of cfDNA with tumor origin has identified tumor biomarkers, elucidating molecular pathology and assisting in accurate diagnosis. In this study, we performed whole-genome sequencing ofcfDNA samples with matching tumor and whole blood samples from five patients diagnosed with stage IV gastric or lung cancer. We analyzed the coverage spectrum of the human genome in our cfDNA samples. cfDNA exhibited no large regions with significant under-coverage, although we observed unbalanced coverage depth in cfDNA at transcription start sites and exon boundaries as a consequence of biased fragmentation due to ordered nucleosome positioning. We also analyzed the copy number variant status based on the whole-genome sequencing results and found high similarity between copy number profile constructed from tumor samples and cfDNA samples. Overall, we conclude that cfDNA comprises a good representation of the tumor genome in late stage gastric and lung cancer.

摘要

游离DNA(cfDNA)是存在于血浆中的短链、细胞外、双链断裂DNA。已发现实体瘤患者的血浆中cfDNA的含量显著增加。尽管目前对cfDNA的产生机制了解甚少,但推测其是细胞凋亡和坏死过程中基因组DNA片段化的产物。对具有肿瘤来源的cfDNA进行测序已鉴定出肿瘤生物标志物,阐明了分子病理学并有助于准确诊断。在本研究中,我们对来自5例诊断为IV期胃癌或肺癌患者的cfDNA样本以及匹配的肿瘤和全血样本进行了全基因组测序。我们分析了cfDNA样本中人类基因组的覆盖谱。尽管由于有序核小体定位导致的片段化偏差,我们在cfDNA的转录起始位点和外显子边界观察到覆盖深度不平衡,但cfDNA未表现出大片段显著低覆盖区域。我们还根据全基因组测序结果分析了拷贝数变异状态,发现从肿瘤样本和cfDNA样本构建的拷贝数图谱高度相似。总体而言,我们得出结论,cfDNA很好地代表了晚期胃癌和肺癌的肿瘤基因组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a80/5207727/fb602ef8417f/pone.0169231.g001.jpg

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