Evidence map›Paper›PMID 41115248›Full record

ArticleJournal of proteome research2025

New Method Enhanced Extraction of Protein Signatures of Renal Cell Carcinoma from Proteomics Data.

Hongyi Liu, Zhuo Ma, T Mamie Lih, Lijun Chen, Yingwei Hu, Yuefan Wang, Zhenyu Sun, Yuanyu Huang, Yuanwei Xu, Hui Zhang

Abstract read
In one paragraph

Article in Journal of proteome 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Hongyi LiuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0000-0002-9444-3632
Zhuo MaKrieger School of Arts and Sciences, Johns Hopkins University, Baltimore, Maryland 21218, United States.
T Mamie LihDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0000-0003-0317-2660
Lijun ChenDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.
Yingwei HuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0000-0002-4629-0985
Yuefan WangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0000-0001-5731-6143
Zhenyu SunDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0009-0002-5004-5904
Yuanyu HuangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0009-0002-5930-8424
Yuanwei XuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.
Hui ZhangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, United States.ORCID 0000-0001-8726-7098

Funding

Proteogenomic Characterization of Tumor Tissues and Preclinical Models with High PrecisionU24CA271079 · NCI · JOHNS HOPKINS UNIVERSITY · PI DANIEL Wanyui CHAN, Hui Zhang · 2022 to 2026
$6.6M
NCI NIH HHS U24 CA271079
6 · The paper itself

Abstract

In this study, we generated label-free data-independent acquisition (DIA)-based liquid chromatography (LC)-mass spectrometry (MS) proteomics data from 261 renal cell carcinomas (RCC) and 195 normal adjacent tissues (NAT). The RCC tumors included 48 nonclear cell renal cell carcinomas (non-ccRCC) and 213 ccRCC. A total of 219,740 peptides and 11,943 protein groups were identified, with 9,787 protein groups per sample on average. We adopted a comprehensive approach to select representative samples with different mutations, considering histopathological, immune, methylation, and non-negative matrix factorization (NMF)-based subtypes, along with clinical characteristics (gender, grade, and stage) to capture the complexity and diversity of ccRCC tumors. We identified a protein signature containing 55 proteins that distinguish RCC tumors from NATs. Furthermore, a protein signature containing 39 proteins that differentiate different RCC tumor subtypes was also identified. Our findings offer an extensive perspective of the proteomic landscape in RCC, illuminating specific proteins that serve to distinguish RCC tumors from NATs and among various RCC tumor subtypes.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellKidney NeoplasmsNeoplasm ProteinsProteomeProteomicsAgedChromatography, LiquidFemaleHumansMaleMass SpectrometryMiddle AgedBiomarkers, TumorNeoplasm ProteinsProteomeclear cell renal cell carcinomaclinical proteomic tumor analysis consortium (CPTAC)data-independent acquisition (DIA)non-clear cell renal cell carcinomaproteomicsrenal cell carcinoma

Identifiers

PMID41115248
PMCPMC13089382

What OpenQuestion holds

Textmetadata
LicenceTDM
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.