Cell-free DNA end characteristics enable accurate and sensitive cancer diagnosis

The fragmentation patterns of cell-free DNA (cfDNA) in plasma can potentially be utilized as diagnostic biomarkers in liquid biopsy. However, our knowledge of this biological process and the information encoded in fragmentation patterns remains preliminary. Here, we investigated the cfDNA fragmentomic characteristics against nucleosome positioning patterns in hematopoietic cells. cfDNA molecules with ends located within nucleosomes were relatively shorter with altered end motif patterns, demonstrating the feasibility of enriching tumor-derived cfDNA in patients with cancer through the selection of molecules possessing such ends. We then developed three cfDNA fragmentomic metrics after end selection, which showed significant alterations in patients with cancer and enabled cancer diagnosis. By incorporating machine learning, we further built high-performance diagnostic models, which achieved an overall area under the curve of 0.95 and 85.1% sensitivity at 95% specificity. Hence, our investigations explored the end characteristics of cfDNA fragmentomics and their merits in building accurate and sensitive cancer diagnostic models.

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Publication Details

Journal
Cell Reports Methods
Published
2024-10-01
DOI
https://doi.org/10.1016/j.crmeth.2024.100877
Citations
19
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
5.42

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article

Cell-free DNA end characteristics enable accurate and sensitive cancer diagnosis

Yunyun An, Zhaohua Xia, Dingxue Hu, Jia Ju et al.
19 citations
Cell Reports Methods
Cancer Genomics and Diagnostics
5.42
article

Cell-free DNA end characteristics enable accurate and sensitive cancer diagnosis

Yunyun An, Zhaohua Xia, Dingxue Hu, Jia Ju, Kun Sun, Xiaoyi Liu, Xin Zhao, Fei Fan, Wanqiu Wang, Ziteng Zhang, Mengqi Yang, Yuqi Pan
article en
19 citations

Abstract

The fragmentation patterns of cell-free DNA (cfDNA) in plasma can potentially be utilized as diagnostic biomarkers in liquid biopsy. However, our knowledge of this biological process and the information encoded in fragmentation patterns remains preliminary. Here, we investigated the cfDNA fragmentomic characteristics against nucleosome positioning patterns in hematopoietic cells. cfDNA molecules with ends located within nucleosomes were relatively shorter with altered end motif patterns, demonstrating the feasibility of enriching tumor-derived cfDNA in patients with cancer through the selection of molecules possessing such ends. We then developed three cfDNA fragmentomic metrics after end selection, which showed significant alterations in patients with cancer and enabled cancer diagnosis. By incorporating machine learning, we further built high-performance diagnostic models, which achieved an overall area under the curve of 0.95 and 85.1% sensitivity at 95% specificity. Hence, our investigations explored the end characteristics of cfDNA fragmentomics and their merits in building accurate and sensitive cancer diagnostic models.

Cell Reports MethodsVol. 4(10)
Union Hospital (HK), Southern University of Science and Technology (CN), Shenzhen Bay Laboratory (CN), Shenzhen Second People's Hospital (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Science, Technology and Innovation Commission of Shenzhen Municipality, Shenzhen Bay Laboratory, Key Technologies Research and Development Program, Basic and Applied Basic Research Foundation of Guangdong Province
Good health and well-being
Openalex Percentile: Top 3%
Cancer Genomics and Diagnostics
5.42
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