Evidence map›Paper›PMID 36653380›Full record

ArticleNature communications2023

DNA methylation analysis explores the molecular basis of plasma cell-free DNA fragmentation.

Yunyun An, Xin Zhao, Ziteng Zhang, Zhaohua Xia, Mengqi Yang, Li Ma, Yu Zhao, Gang Xu, Shunda Du, Xiang'an Wu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
23.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 97 citations in OpenAlex.

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  20. Cancer-Like Fragmentomic Characteristics of Somatic Variants in Cell-Free DNA.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article

19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 1 country.

Yunyun AnInstitute of Cancer Research, Shenzhen Bay Laboratory, 518132, Shenzhen, China.
Xin ZhaoHepato-Biliary Surgery Division, Shenzhen Third People's Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, 518100, Shenzhen, China.
Ziteng ZhangHepato-Biliary Surgery Division, Shenzhen Third People's Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, 518100, Shenzhen, China.
Zhaohua XiaThoracic Surgical Department, Shenzhen Third People's Hospital, The Second Affiliated Hospital, Southern University of Science and Technology, 518100, Shenzhen, China.
Mengqi YangInstitute of Cancer Research, Shenzhen Bay Laboratory, 518132, Shenzhen, China.
Li MaInstitute of Cancer Research, Shenzhen Bay Laboratory, 518132, Shenzhen, China.
Yu ZhaoMolecular Cancer Research Center, School of Medicine, Shenzhen Campus of Sun Yat-sen University, Sun Yat-sen University, 518107, Shenzhen, China.
Gang XuDepartment of Liver Surgery and Liver Transplant Center, West China Hospital of Sichuan University, 610041, Chengdu, China.
Shunda DuDepartment of Liver Surgery, Peking Union Medical College Hospital, PUMC and Chinese Academy of Medical Sciences, 100730, Beijing, Dongcheng, China.ORCID 0000-0002-9357-3259
Xiang'an WuDepartment of Liver Surgery, Peking Union Medical College Hospital, PUMC and Chinese Academy of Medical Sciences, 100730, Beijing, Dongcheng, China.
Shuowen ZhangDepartment of Liver Surgery, Peking Union Medical College Hospital, PUMC and Chinese Academy of Medical Sciences, 100730, Beijing, Dongcheng, China.ORCID 0000-0002-1466-1788
Xin HongDepartment of Biochemistry, School of Medicine, Southern University of Science and Technology, 518055, Shenzhen, China.
Xin JinBGI-Shenzhen, 518083, Shenzhen, China. jinxin@genomics.cn.ORCID 0000-0001-7554-4975
Kun SunInstitute of Cancer Research, Shenzhen Bay Laboratory, 518132, Shenzhen, China. sunkun@szbl.ac.cn.ORCID 0000-0002-9883-1616
Shenzhen Bay Laboratory · CNSouthern University of Science and Technology · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNBGI Group (China) · CNSichuan University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma cell-free DNA (cfDNA) are small molecules generated through a non-random fragmentation procedure. Despite commendable translational values in cancer liquid biopsy, however, the biology of cfDNA, especially the principles of cfDNA fragmentation, remains largely elusive. Through orientation-aware analyses of cfDNA fragmentation patterns against the nucleosome structure and integration with multidimensional functional genomics data, here we report a DNA methylation - nuclease preference - cutting end - size distribution axis, demonstrating the role of DNA methylation as a functional molecular regulator of cfDNA fragmentation. Hence, low-level DNA methylation could increase nucleosome accessibility and alter the cutting activities of nucleases during DNA fragmentation, which further leads to variation in cutting sites and size distribution of cfDNA. We further develop a cfDNA ending preference-based metric for cancer diagnosis, whose performance has been validated by multiple pan-cancer datasets. Our work sheds light on the molecular basis of cfDNA fragmentation towards broader applications in cancer liquid biopsy.

Indexed as

Cell-Free Nucleic AcidsNeoplasmsBiomarkers, TumorDNA FragmentationDNA MethylationHumansNucleosomesBiomarkers, TumorCell-Free Nucleic AcidsNucleosomes

Identifiers

PMID36653380
PMCPMC9849216
OpenAlexW4317209249

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.