Evidence map›Paper›PMID 41046245›Full record

ArticleBritish journal of cancer2025

Distinct prognostic and molecular profiles of fat versus vein invasion in T3a renal cell carcinoma.

Hyun Young Lee, Ray Raehun Lee, Yunlim Kim, Ji-Hye Oh, Jungyo Suh, Chang-Wook Jeong, Cheol Kwak, Minyong Kang, Seong Il Seo, Ha-Na Woo and 3 more

Abstract read
In one paragraph

Article in British journal of cancer, 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. Review
  2. 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

13 authors.

Hyun Young Lee *Department of Urology, Soonchunhyang University Seoul Hospital, Seoul, Korea.
Ray Raehun Lee *Department of Urology, Asan Medical Center, Seoul, Korea.
Yunlim KimDepartment of Urology, Asan Medical Center, Seoul, Korea.
Ji-Hye OhDepartment of Bioinformatics Core Laboratory, Convergence Medicine Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Jungyo SuhDepartment of Urology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Chang-Wook JeongDepartment of Urology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Cheol KwakDepartment of Urology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Minyong KangDepartment of Urology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Seong Il SeoDepartment of Urology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Ha-Na WooDepartment of Biochemistry, University of Ulsan College of Medicine, Seoul, Korea.
Heuiran LeeDepartment of Microbiology, University of Ulsan College of Medicine, Seoul, Korea.
Chang Ohk SungDepartment of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.ORCID http://orcid.org/0000-0002-8567-456X
Cheryn SongDepartment of Urology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea. cherynsong@amc.seoul.kr.ORCID http://orcid.org/0000-0002-1823-4281

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundpT3a renal cell carcinoma (RCC) encompasses three different types of progression features leading to persistent debate on prognostic heterogeneity and the need for reclassification.

methodsData of 1606 patients with pT3aN0/xM0 RCC was analyzed according to the site of invasion (perinephric fat (PFI), sinus fat (SFI), renal vein (RVI), PFI and SFI without RVI (PFI + SFI), and both fat and vein (RVI + FI)) using Kaplan-Meier and Cox proportional hazards methods. RNA sequencing was performed on tumor samples from 19 SFI and 14 RVI patients to identify differentially expressed genes and pathway enrichments.

resultsFive-year DFS were 76%, 68.5%, 62.4%, 63.9%, and 50.1% for SFI, PFI, PFI + SFI, RVI and RVI + FI groups, respectively (p < 0.001). Vein invasion tumors demonstrating consistently poorer survival on size-stratified analysis. Site of invasion was an independent prognostic factor. Transcriptomic profiling revealed that SFI tumors were enriched for epithelial-mesenchymal transition, KRAS signaling, and extracellular matrix reprogramming, whereas RVI tumors exhibited hypoxia, oxidative phosphorylation, and DNA repair pathway activation.

conclusionIn T3a RCC, site of invasion was an independent prognosticator of survival regardless of tumor size. SFI and RVI tumors exhibited distinct genomic and pathway profiles suggesting an intrinsically disparate competencies directing the tumors to adopt different invasion mechanisms.

Indexed as

Adipose TissueCarcinoma, Renal CellKidney NeoplasmsRenal VeinsAdultAgedFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessPrognosisTranscriptome

Identifiers

PMID41046245
PMCPMC12690098

What OpenQuestion holds

Textmetadata
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.