Evidence map›Paper›PMID 38191424›Full record

ArticleJournal of translational medicine2024

Single-cell transcriptome sequencing reveals aberrantly activated inter-tumor cell signaling pathways in the development of clear cell renal cell carcinoma.

Junfeng Zhang, Fuzhong Liu, Wenjia Guo, Xing Bi, Shuai Yuan, Fuerhaiti Shayiti, Ting Pan, Kailing Li, Peng Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-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

17 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

9 authors at 2 institutions in 1 country.

Junfeng ZhangDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.ORCID 0000-0002-3511-8055
Fuzhong LiuCancer Institute, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Wenjia GuoCancer Institute, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Xing BiDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Shuai YuanDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Fuerhaiti ShayitiDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Ting PanDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Kailing LiDepartment of Urology, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, No. 158 Wuyang Avenue, Enshi, 445000, Hubei, China. 726589787@qq.com.
Peng ChenDepartment of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China. chenpeng9@126.com.
Xinjiang Medical University · CNThe Central Hospital of Enshi Tujia and Miao Autonomous Prefecture · CN

Funding

The National Natural Science Foundation of China No. 82260791
6 · The paper itself

Abstract

backgroundAberrant intracellular or intercellular signaling pathways are important mechanisms that contribute to the development and progression of cancer. However, the intercellular communication associated with the development of ccRCC is currently unknown. The purpose of this study was to examine the aberrant tumor cell-to-cell communication signals during the development of ccRCC.

methodsWe conducted an analysis on the scRNA-seq data of 6 ccRCC and 6 normal kidney tissues. This analysis included sub clustering, CNV analysis, single-cell trajectory analysis, cell-cell communication analysis, and transcription factor analysis. Moreover, we performed validation tests on clinical samples using multiplex immunofluorescence.

resultsThis study identified eleven aberrantly activated intercellular signaling pathways in tumor clusters from ccRCC samples. Among these, two of the majors signaling molecules, MIF and SPP1, were mainly secreted by a subpopulation of cancer stem cells. This subpopulation demonstrated high expression levels of the cancer stem cell markers POU5F1 and CD44 (POU5F1

conclusionAberrantly activated tumor intercellular signaling pathways promote the development and progression of ccRCC. The cancer stem cell subpopulation (POU5F1

Indexed as

Carcinoma, Renal CellKidney NeoplasmsCell CommunicationHumansSignal TransductionTranscriptomeCancer stem cellsCell communicationClear cell renal cell carcinomaSingle-cell RNA sequencingSPP1 signaling pathway

Identifiers

PMID38191424
PMCPMC10775677
OpenAlexW4390675542

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.