Evidence map›Paper›PMID 37081700›Full record

ArticleCancer medicine2023

Clear cell renal cell carcinoma molecular variations in non-Hispanic White and Hispanic patients.

Ken Batai, Yuliang Chen, Brenna A Rheinheimer, Amit Arora, Ritu Pandey, Ronald L Heimark, Erika R Bracamonte, Nathan A Ellis, Benjamin R Lee

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. 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
0.5field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  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

9 authors at 2 institutions in 1 country.

Ken BataiDepartment of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.ORCID 0000-0002-0317-1118
Yuliang ChenDepartment of Epidemiology and Biostatistics, University of Arizona, Tucson, Arizona, USA.
Brenna A RheinheimerDepartment of Nutritional Sciences, University of Arizona, Tucson, Arizona, USA.
Amit AroraDepartment of Epidemiology and Biostatistics, University of Arizona, Tucson, Arizona, USA.
Ritu PandeyDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, Arizona, USA.
Ronald L HeimarkDepartment of Surgery, University of Arizona, Tucson, Arizona, USA.
Erika R BracamonteDepartment of Pathology, University of Arizona, Tucson, Arizona, USA.
Nathan A EllisDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, Arizona, USA.
Benjamin R LeeDepartment of Urology, University of Arizona, Tucson, Arizona, USA.
University of Arizona · USRoswell Park Comprehensive Cancer Center · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
NCI NIH HHS P30 CA023074
6 · The paper itself

Abstract

backgroundThe United States is becoming increasingly diverse, but few molecular studies have assessed the progression of clear cell renal cell carcinoma (ccRCC) in diverse patient populations. This study examined ccRCC molecular variations in non-Hispanic White (NHW) and Hispanic patients and their effect on the association of gene expression with high-grade (Grade 3 or 4) ccRCC and overall mortality.

methodsA total of 156 patients were included in VHL sequencing and/or TempO-Seq analysis. DESeq2 was used to identify the genes associated with high-grade ccRCC. Logistic regression analysis was performed to assess whether race and ethnicity was associated with high/moderate impact VHL somatic mutations and the ccA/ccB subtype. Cox regression analysis was performed to assess association of molecular subtype and gene expression with overall mortality.

resultsNHWs had moderate or high impact mutations in the VHL gene at a higher frequency than Hispanics (40.2% vs. 27.4%), while Hispanics had a higher frequency of the ccA subtype than NHWs (61.9% vs. 45.8%). ccA was more common in patients with BMI≥35 (65.2%) than in those with BMI < 25 (45.0%). There were 11 differentially expressed genes between high- and low-grade tumors. The Haptoglobin (HP) gene was most significantly overexpressed in high- compared to low-grade ccRCC in all samples (p-adj = 1.7 × 10

conclusionThis study reports ccRCC molecular variations in Hispanic patients who were previously underrepresented.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsEthnicityHispanic or LatinoHumansWhitegene expression and diversity Hispanics and European Americans (comparison)health disparitiesmolecular subtypeVHL

Identifiers

PMID37081700
PMCPMC10278477
OpenAlexW4366602930

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.