Evidence map›Paper›PMID 31100982›Full record

ArticleCancers2019

Integrative Metabolomic and Transcriptomic Analysis for the Study of Bladder Cancer.

Alba Loras, Cristian Suárez-Cabrera, M Carmen Martínez-Bisbal, Guillermo Quintás, Jesús M Paramio, Ramón Martínez-Máñez, Salvador Gil, José Luis Ruiz-Cerdá

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. Metabolomic profiling of human bladder tissue extracts.Metabolomics : Official journal of the Metabolomic Society · 2024
    Article
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  10. Review
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  12. Article
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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 5 institutions in 1 country.

Alba LorasUnidad Mixta de Investigación en Nanomedicina y Sensores, Universitat Politècnica de València-Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain. lomonal@alumni.uv.es.ORCID 0000-0003-1426-1765
Cristian Suárez-CabreraGrupo de Oncología Celular y Molecular, Hospital Universitario 12 de Octubre, 28041 Madrid, Spain. cristian.suarez@externos.ciemat.es.ORCID 0000-0003-1897-1596
M Carmen Martínez-BisbalUnidad Mixta de Investigación en Nanomedicina y Sensores, Universitat Politècnica de València-Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain. mamarbis@upvnet.upv.es.ORCID 0000-0002-8526-4413
Guillermo QuintásAnalytical Unit, IIS La Fe, 46026 Valencia, Spain. gquintas@leitat.org.ORCID 0000-0002-4240-9846
Jesús M ParamioGrupo de Oncología Celular y Molecular, Hospital Universitario 12 de Octubre, 28041 Madrid, Spain. jesusm.paramio@ciemat.es.ORCID 0000-0001-7520-3177
Ramón Martínez-MáñezUnidad Mixta de Investigación en Nanomedicina y Sensores, Universitat Politècnica de València-Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain. rmaez@qim.upv.es.ORCID 0000-0001-5873-9674
Salvador GilInstituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico, Universitat Politècnica de València, Universitat de València, 46022 Valencia, Spain. salvador.gil@uv.es.ORCID 0000-0002-2818-1320
José Luis Ruiz-CerdáUnidad Mixta de Investigación en Nanomedicina y Sensores, Universitat Politècnica de València-Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain. jose.l.ruiz@uv.es.
Universitat de València · ESHospital Universitario 12 De Octubre · ESHospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ESLeitat Technological Center · ES

Funding

PDGF Regulation of Cell Growth and DeathR01CA064139 · NCI · WAYNE STATE UNIVERSITY · PI KIM, HYEONG-REH CHOI · 2002 to 2006
$1.3M
MECHANISM OF PDGF INDUCED APOPTOSISR29CA064139 · NCI · WAYNE STATE UNIVERSITY · PI KIM, HYEONG-REH CHOI · 1996 to 2001
$147k
HIGH RESOLUTION X RAY DETECTORS FOR DIGITAL MAMMOGRAPHYR01CA066015 · NCI · SUNNYBROOK &WOMEN'S COLL HLTH SCIS CTR · PI YAFFE, MARTIN J · 1994 to 1996
–
Conselleria d'Educació, Investigació, Cultura i Esport PROMETEO 2018/24Conselleria d'Educació, Investigació, Cultura i Esport PROMETEO II/2014/047Ministerio de Ciencia e Innovación CB/16/00228Ministerio de Ciencia e Innovación CTQ2016-79561-PMinisterio de Ciencia e Innovación ISCIII-RETICRD12/0036/0009Ministerio de Ciencia e Innovación MAT2015-64139-C4-1-RMinisterio de Ciencia e Innovación MAT2015-64139-C4-3-RMinisterio de Ciencia e Innovación SAF2015-66015-R
6 · The paper itself

Abstract

Metabolism reprogramming is considered a hallmark of cancer. The study of bladder cancer (BC) metabolism could be the key to developing new strategies for diagnosis and therapy. This work aimed to identify tissue and urinary metabolic signatures as biomarkers of BC and get further insight into BC tumor biology through the study of gene-metabolite networks and the integration of metabolomics and transcriptomics data. BC and control tissue samples (n = 44) from the same patients were analyzed by High-Resolution Magic Angle Spinning Nuclear Magnetic Resonance and microarrays techniques. Besides, urinary profiling study (n = 35) was performed in the same patients to identify a metabolomic profile, linked with BC tissue hallmarks, as a potential non-invasive approach for BC diagnosis. The metabolic profile allowed for the classification of BC tissue samples with a sensitivity and specificity of 100%. The most discriminant metabolites for BC tissue samples reflected alterations in amino acids, glutathione, and taurine metabolic pathways. Transcriptomic data supported metabolomic results and revealed a predominant downregulation of metabolic genes belonging to phosphorylative oxidation, tricarboxylic acid cycle, and amino acid metabolism. The urinary profiling study showed a relation with taurine and other amino acids perturbed pathways observed in BC tissue samples, and classified BC from non-tumor urine samples with good sensitivities (91%) and specificities (77%). This urinary profile could be used as a non-invasive tool for BC diagnosis and follow-up.

Indexed as

bladder cancercancer biomarkerscancer metabolic reprogrammingmetabolic pathwaysmetabolomicstranscriptomicstumor metabolome

Identifiers

PMID31100982
PMCPMC6562847
OpenAlexW2945550220

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.