Distinct Features of Plasma Ultrashort Single-Stranded Cell-Free DNA as Biomarkers for Lung Cancer Detection

被引:4
作者
Cheng, Jordan [1 ]
Swarup, Neeti [1 ]
Li, Feng [1 ]
Kordi, Misagh [1 ]
Lin, Chien-Chung [2 ]
Yang, Szu-Chun [2 ]
Huang, Wei-Lun [3 ]
Aziz, Mohammad [1 ]
Kim, Yong [1 ]
Chia, David [4 ]
Yeh, Yu-Min [3 ,5 ]
Wei, Fang [1 ]
Zheng, David [6 ]
Zhang, Liying [4 ]
Pellegrini, Matteo [6 ]
Su, Wu-Chou [3 ,5 ,8 ]
Wong, David T. W. [1 ,7 ]
机构
[1] Univ Calif Los Angeles, Sch Dent, Los Angeles, CA USA
[2] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Internal Med, Tainan, Taiwan
[3] Natl Cheng Kung Univ, Ctr Appl Nanomed, Tainan, Taiwan
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA USA
[5] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Oncol, Tainan, Taiwan
[6] Univ Calif Los Angeles, Life Sci Div, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
[7] Univ Calif Los Angeles, Sch Dent, Los Angeles, CA 90095 USA
[8] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Oncol, Tainan 701, Taiwan
关键词
ORIGIN;
D O I
10.1093/clinchem/hvad131
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Using broad range cell-free DNA sequencing (BRcfDNA-Seq), a nontargeted next-generation sequencing (NGS) methodology, we previously identified a novel class of approximately 50 nt ultrashort single-stranded cell-free DNA (uscfDNA) in plasma that is distinctly different from 167 bp mononucleosomal cell-free DNA (mncfDNA). We hypothesize that uscfDNA possesses characteristics that are useful for disease detection. METHODS: Using BRcfDNA-Seq, we examined both cfDNA populations in the plasma of 18 noncancer controls and 14 patients with late-stage nonsmall cell lung carcinoma (NSCLC). In comparison to mncfDNA, we assessed whether functional element (FE) peaks, fragmentomics, end-motifs, and G-Quadruplex (G-Quad) signatures could be useful features of uscfDNA for NSCLC determination. RESULTS: In noncancer participants, compared to mncfDNA, uscfDNA fragments showed a 45.2-fold increased tendency to form FE peaks (enriched in promoter, intronic, and exonic regions), demonstrated a distinct end-motif-frequency profile, and presented with a 4.9-fold increase in G-Quad signatures. Within NSCLC participants, only the uscfDNA population had discoverable FE peak candidates. Additionally, uscfDNA showcased different end-motif-frequency candidates distinct from mncfDNA. Although both cfDNA populations showed increased fragmentation in NSCLC, the G-Quad signatures were more discriminatory in uscfDNA. Compilation of cfDNA features using principal component analysis revealed that the first 5 principal components of both cfDNA subtypes had a cumulative explained variance of >80%. CONCLUSIONS: These observations indicate that the distinct biological processes of uscfDNA and that FE peaks, fragmentomics, end-motifs, and G-Quad signatures are uscfDNA features with promising biomarker potential. These findings further justify its exploration as a distinct class of biomarker to augment pre-existing liquid biopsy approaches.
引用
收藏
页码:1270 / 1282
页数:13
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