Evidence map›Paper›PMID 38817335›Full record

ArticleWorld journal of stem cells2024

Therapeutic potential of urine-derived stem cells in renal regeneration following acute kidney injury: A comparative analysis with mesenchymal stem cells.

Fang Li, Bin Zhao, Lei Zhang, Guo-Qing Chen, Li Zhu, Xiao-Ling Feng, Meng-Jia Gong, Cheng-Chen Hu, Yuan-Yuan Zhang, Ming Li and 1 more

Abstract read
In one paragraph

Article in World journal of stem cells, 2024. 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
–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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Tracking of Urine-Derived Stem Cells in Mice.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Review
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.

Fang LiDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Bin ZhaoDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Lei ZhangDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Guo-Qing ChenDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Li ZhuDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Xiao-Ling FengDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China.
Meng-Jia GongDepartment of Pediatric Research Institute, Children's Hospital of Chongqing Medical University, Chongqing 401147, China.
Cheng-Chen HuDepartment of Pediatric Research Institute, Children's Hospital of Chongqing Medical University, Chongqing 401147, China.
Yuan-Yuan ZhangDepartment of Pediatric Research Institute, Children's Hospital of Chongqing Medical University, Chongqing 401147, China.
Ming LiDepartment of Pediatric Research Institute, Children's Hospital of Chongqing Medical University, Chongqing 401147, China.
Yong-Qiang LiuDepartment of General Surgery, Chongqing General Hospital, Chongqing 401147, China. wklyq007@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is a common clinical syndrome with high morbidity and mortality rates. The use of pluripotent stem cells holds great promise for the treatment of AKI. Urine-derived stem cells (USCs) are a novel and versatile cell source in cell-based therapy and regenerative medicine that provide advantages of a noninvasive, simple, and low-cost approach and are induced with high multidifferentiation potential. Whether these cells could serve as a potential stem cell source for the treatment of AKI has not been determined.

aimTo investigate whether USCs can serve as a potential stem cell source to improve renal function and histological structure after experimental AKI.

methodsStem cell markers with multidifferentiation potential were isolated from human amniotic fluid. AKI severe combined immune deficiency (SCID) mice models were induced by means of an intramuscular injection with glycerol. USCs isolated from human-voided urine were administered

resultsTreatment with USCs significantly alleviated histological destruction and functional decline. The renal function was rapidly restored after intravenous injection of 5 × 10

conclusionOur study demonstrated the potential of USCs for the treatment of AKI, representing a new clinical therapeutic strategy.

Indexed as

Acute kidney injuryCell therapyRegenerative medicineRenal function recoveryUrine-derived stem cells

Identifiers

PMID38817335
PMCPMC11135250

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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.