Evidence map›Paper›PMID 38017497›Full record

ArticleStem cell research & therapy2023

Deciphering the role of extrachromosomal circular DNA in adipose stem cells from old and young donors.

Sen Ren, Du Wu, Xiaoyong Shen, Qian Wu, Chengcheng Li, Hewei Xiong, Zhongwei Xiong, Rui Gong, Zheng Liu, Wei Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Extrachromosomal Circular DNA and Transposable Elements in Type 2 Diabetes.International journal of molecular sciences · 2025
    Review
  2. Review
  3. Article
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  10. A scATAC-seq atlas of stasis zone in rat skin burn injury wound process.Frontiers in cell and developmental biology · 2024
    Article
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

11 authors at 2 institutions in 1 country.

Sen RenDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Du WuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Xiaoyong ShenHospital of Stomatology Wuhan University, Wuhan, 430079, China.
Qian WuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Chengcheng LiDepartment of Hand Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Hewei XiongDepartment of Emergency Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Zhongwei XiongDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Rui GongDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Zheng LiuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. liuzheng@znhospital.cn.
Wei WangDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. wangwei820805@hotmail.com.
Jincao ChenDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. chenjc2020@126.com.ORCID 0000-0001-9882-7978
Wuhan University · CNUnion Hospital · CN

Funding

Fundamental Research Funds for the Central Universities 2042022kf1142
6 · The paper itself

Abstract

backgroundThe functional impairment of adipose stem cells (ASCs) during aging limits their clinical transformation. Studies have shown that extrachromosomal circular DNAs (eccDNAs) are associated with tumor progression and cell aging, but the roles of eccDNAs in ASCs remain unknown.

methodWe conducted Circle sequencing (Circle-seq) to identify eccDNAs in ASCs isolated from young and old donors. The differentially expressed eccDNAs were calculated, annotated and validated via polymerase chain reaction.

resultsThousands of eccDNAs were identified and comprehensively characterized. Most of them were GC-rich, < 1000 base pairs in size, and were enriched on chromosome 19 and 17 with a high density of Alu elements and genes, 2 kb upstream/downstream of genes and satellites. In total, 3025 eccDNAs were differentially expressed among the two ASC groups. Conjoint analysis of the Circle-seq results and previous RNA-seq results revealed that 73 eccDNAs and 55 genes exhibited the same differential expression between the two groups. KEGG and GO analyses revealed that genes encoding differentially expressed eccDNAs were enriched for cell adhesion, cellular senescence and TGF-β receptor signaling pathway. We also found that aged ASCs exhibited loss of eccDNAs, including CAMK2G

conclusionIn this study, we elucidated the first eccDNA profile relating to ASCs and demonstrated that three eccDNAs are lost in aged ASCs, which may be potential biomarkers of stem cell aging and valuable targets for stem cell rejuvenation.

Indexed as

DNADNA, CircularBiomarkersPolymerase Chain ReactionBiomarkersDNADNA, CircularAdipose stem cellAgingExtrachromosomal circular DNA

Identifiers

PMID38017497
PMCPMC10683086
OpenAlexW4389086937

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Registered trials

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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.