Evidence map›Paper›PMID 33661419›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2021

Metabolomic and elemental profiling of human tissue in kidney cancer.

Joanna Nizioł, Valérie Copié, Brian P Tripet, Leonardo B Nogueira, Katiane O P C Nogueira, Krzysztof Ossoliński, Adrian Arendowski, Tomasz Ruman

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2021. 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
2.0field-weighted citation impact, top 13% 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, 35 citations in OpenAlex.

  1. Article
  2. Broadband Collision-Induced Dissociation Mass Spectrometry Imaging.Journal of the American Society for Mass Spectrometry · 2025
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  11. Metabolomic profiling of human bladder tissue extracts.Metabolomics : Official journal of the Metabolomic Society · 2024
    Article
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  13. Review
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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

8 authors at 4 institutions in 3 countries.

Joanna NiziołFaculty of Chemistry, Rzeszów University of Technology, 6 Powstańców Warszawy Ave., 35-959, Rzeszów, Poland. jniziol@prz.edu.pl.ORCID 0000-0002-4783-8615
Valérie CopiéThe Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT, 59717, USA.
Brian P TripetThe Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT, 59717, USA.
Leonardo B NogueiraDepartment of Geology, Federal University of Ouro Preto, Ouro Preto, Minas Gerais, Brazil.
Katiane O P C NogueiraDepartment of Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Minas Gerais, Brazil.
Krzysztof OssolińskiDepartment of Urology, John Paul II Hospital, Grunwaldzka 4 St., 36-100, Kolbuszowa, Poland.
Adrian ArendowskiFaculty of Chemistry, Rzeszów University of Technology, 6 Powstańców Warszawy Ave., 35-959, Rzeszów, Poland.
Tomasz RumanFaculty of Chemistry, Rzeszów University of Technology, 6 Powstańców Warszawy Ave., 35-959, Rzeszów, Poland.
Rzeszów University of Technology · PLMontana State University · USUniversidade Federal de Ouro Preto · BRJohn Paul II Hospital · PL

Funding

Acquisition of a 600 MHz NMR cryoprobe and 600 MHz spectrometer console upgradeS10RR026659 · NCRR · MONTANA STATE UNIVERSITY - BOZEMAN · PI COPIE, VALERIE · 2011 to 2011
$600k
NCRR NIH HHS S10 RR026659
6 · The paper itself

Abstract

introductionKidney cancer is one of the most frequently diagnosed and the most lethal urinary cancer. Despite advances in treatment, no specific biomarker is currently in use to guide therapeutic interventions.

objectivesMajor aim of this work was to perform metabolomic and elemental profiling of human kidney cancer and normal tissue and to evaluate cancer biomarkers.

methodsMetabolic and elemental profiling of tumor and adjacent normal human kidney tissue from 50 patients with kidney cancer was undertaken using three different analytical methods.

resultsFive potential tissue biomarkers of kidney cancer were identified and quantified using with high-resolution nuclear magnetic resonance spectroscopy. The contents of selected chemical elements in tissues was analyzed using inductively coupled plasma optical emission spectrometry. Eleven mass spectral features differentiating between kidney cancer and normal tissues were detected using silver-109 nanoparticle enhanced steel target laser desorption/ionization mass spectrometry.

conclusionsOur results, derived from the combination of ICP-OES, LDI MS and 1H NMR methods, suggest that tissue biomarkers identified herein appeared to have great potential for use in clinical prognosis and/or diagnosis of kidney cancer.

Indexed as

AgedBiomarkers, TumorFemaleHumansIsotopesKidneyKidney NeoplasmsMagnetic Resonance SpectroscopyMaleMetabolomicsMultivariate AnalysisSilverBiomarkers, TumorIsotopesSilverSilver-109BiomarkersCancerHuman kidney tissueMetabolomicsMetallomics

Identifiers

PMID33661419
PMCPMC7932981
OpenAlexW3134292496

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.