Evidence map›Paper›PMID 35474296›Full record

ArticleClinical and translational medicine2022

Circle-Seq reveals genomic and disease-specific hallmarks in urinary cell-free extrachromosomal circular DNAs.

Wei Lv, Xiaoguang Pan, Peng Han, Ziyu Wang, Weijia Feng, Xue Xing, Qingqing Wang, Kunli Qu, Yuchen Zeng, Cailin Zhang and 17 more

Abstract read
In one paragraph

Article in Clinical and translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

52 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Extrachromosomal Circular DNA and Transposable Elements in Type 2 Diabetes.International journal of molecular sciences · 2025
    Review
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  14. Article
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  16. EccDNA-Driven VPS41 Amplification Alleviates Genotoxic Stress via Lysosomal KAI1 Degradation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

Wei LvCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Xiaoguang PanLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Peng HanLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Ziyu WangLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Weijia FengEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Xue XingDepartment of Nephrology, Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Qingqing WangCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Kunli QuLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Yuchen ZengIBMC-BGI Center, the Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, China.
Cailin ZhangDepartment of Nephrology, Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhe XuCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Yi LiBeijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.
Tianyu ZhengCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Ling LinLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Chengxun LiuCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Xuemei LiuLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Hanbo LiLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Rasmus Amund HenriksenEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Lars BolundLars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.
Lin LinDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Xin JinBGI-Shenzhen, Shenzhen, China.
Huanming YangCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Xiuqing ZhangCollege of Life Sciences, University of Chinese Academy of Science, Beijing, China.
Tailang YinDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, China.
Birgitte RegenbergEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Fan HeDepartment of Nephrology, Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0002-2487-5827
Yonglun LuoIBMC-BGI Center, the Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, China.ORCID 0000-0002-0007-7759

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtrachromosomal circular deoxyribonucleic acid (eccDNA) is evolving as a valuable biomarker, while little is known about its presence in urine.

methodsHere, we report the discovery and analysis of urinary cell-free eccDNAs (ucf-eccDNAs) in healthy controls and patients with advanced chronic kidney disease (CKD) by Circle-Seq.

resultsMillions of unique ucf-eccDNAs were identified and comprehensively characterised. The ucf-eccDNAs are GC-rich. Most ucf-eccDNAs are less than 1000 bp and are enriched in four pronounced peaks at 207, 358, 553 and 732 bp. Analysis of the genomic distribution of ucf-eccDNAs shows that eccDNAs are found on all chromosomes but enriched on chromosomes 17, 19 and 20 with a high density of protein-coding genes, CpG islands, short interspersed transposable elements (SINEs) and simple repeat elements. Analysis of eccDNA junction sequences further suggests that microhomology and palindromic repeats might be involved in eccDNA formation. The ucf-eccDNAs in CKD patients are significantly higher than those in healthy controls. Moreover, eccDNA with miRNA genes is highly enriched in CKD ucf-eccDNA.

conclusionsThis work discovers and provides the first deep characterisation of ucf-eccDNAs and suggests ucf-eccDNA as a valuable noninnvasive biomarker for urogenital disorder diagnosis and monitoring.

Indexed as

DNA, CircularRenal Insufficiency, ChronicBiomarkersDNAFemaleGenomicsHumansMaleBiomarkersDNADNA, Circularcell-free DNAchronic kidney diseaseearly diagnosisextrachromosomal circular DNAmiRNAnext generation sequencingnoninvasive biomarkers

Identifiers

PMID35474296
PMCPMC9042798

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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.