Evidence map›Paper›PMID 40979497›Full record

ArticleJournal of inflammation research2025

Single-Cell RNA Sequencing Reveals Cellular Heterogeneity and Microenvironmental Remodeling in Human Ureteral Scar Stricture Tissue.

Xiaobo Ding, Guoxiang Li, Yuehan Yang, Zhengyao Song, Xudong Shen, Bingbing Hou, Meng Zhang, Shifang Sang, Jian Dai, Jiankang Zhang and 3 more

Abstract read
In one paragraph

Article in Journal of inflammation research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Xiaobo Ding *Department of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Guoxiang Li *Department of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Yuehan Yang *Department of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Zhengyao SongDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Xudong ShenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Bingbing HouDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Meng ZhangDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.ORCID 0000-0003-4935-4005
Shifang SangDepartment of Urology, Lu'an People's Hospital of Anhui Province, Lu'an, Anhui, People's Republic of China.
Jian DaiDepartment of Otorhinolaryngology, Lu'an People's Hospital of Anhui Province, Lu'an, Anhui, People's Republic of China.
Jiankang ZhangDepartment of Infectious Diseases, Lu'an People's Hospital of Anhui Province, Lu'an, Anhui, People's Republic of China.
Zongyao HaoDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Yang ChenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Chaozhao LiangDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study aimed to construct a comprehensive single-cell transcriptomic atlas of human ureteral scar stricture tissue using single-cell RNA sequencing (scRNA-seq), to uncover cellular heterogeneity, subpopulation dynamics, and intercellular communication networks. Methods: Ureteral tissues were collected from three normal controls (CTR) and three patients with ureteral scar stricture (US). Single-cell suspensions were prepared using the MobiNova-100 platform and sequenced on the Illumina NovaSeq 6000 system. Data were analyzed using Seurat, Harmony, Monocle2 (for pseudotime trajectory analysis), CellChat (for cell-cell communication), and SCP (for GO/KEGG enrichment). Key findings were validated by multiplex immunofluorescence (IF) and immunohistochemistry (IHC). Results: Eleven major cell types were identified, including epithelial, stromal, endothelial, and immune cells, each comprising distinct subpopulations. Compared to CTR tissues, US tissues exhibited an increased proportion of S100A8 Conclusion: This study presents the first high-resolution single-cell atlas of ureteral scar stricture tissue, revealing profound cellular heterogeneity and remodeling of the immune-stromal-epithelial landscape. The findings also highlight intensified intercellular communication within the fibrotic microenvironment, offering novel insights into disease pathogenesis and potential therapeutic targets.

Indexed as

cell-cell communicationimmune microenvironmentsingle-cell rna sequencingureteral stricture

Identifiers

PMID40979497
PMCPMC12449274

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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.