Evidence map›Paper›PMID 35954418›Full record

ArticleCancers2022

Prognostic Gene Expression-Based Signature in Clear-Cell Renal Cell Carcinoma.

Fiorella L Roldán, Laura Izquierdo, Mercedes Ingelmo-Torres, Juan José Lozano, Raquel Carrasco, Alexandra Cuñado, Oscar Reig, Lourdes Mengual, Antonio Alcaraz

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 36 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Fiorella L RoldánLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Laura IzquierdoLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0001-6015-2987
Mercedes Ingelmo-TorresLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Juan José LozanoPlataforma de Bioinformàtica, Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBERehd), Hospital Clínic, 08036 Barcelona, Spain.
Raquel CarrascoLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Alexandra CuñadoLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Oscar ReigServei d'Oncologia Mèdica, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Lourdes MengualLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.ORCID 0000-0001-7418-9422
Antonio AlcarazLaboratori i Servei d'Urologia, Hospital Clínic de Barcelona, 08036 Barcelona, Spain.
Hospital Clínic de Barcelona · ESCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESDepartament de Salut · ES

Funding

Hospital Clínic de Barcelona FRC2019
6 · The paper itself

Abstract

The inaccuracy of the current prognostic algorithms and the potential changes in the therapeutic management of localized ccRCC demands the development of an improved prognostic model for these patients. To this end, we analyzed whole-transcriptome profiling of 26 tissue samples from progressive and non-progressive ccRCCs using Illumina Hi-seq 4000. Differentially expressed genes (DEG) were intersected with the RNA-sequencing data from the TCGA. The overlapping genes were used for further analysis. A total of 132 genes were found to be prognosis-related genes. LASSO regression enabled the development of the best prognostic six-gene panel. Cox regression analyses were performed to identify independent clinical prognostic parameters to construct a combined nomogram which includes the expression of CERCAM, MIA2, HS6ST2, ONECUT2, SOX12, TMEM132A, pT stage, tumor size and ISUP grade. A risk score generated using this model effectively stratified patients at higher risk of disease progression (HR 10.79; p < 0.001) and cancer-specific death (HR 19.27; p < 0.001). It correlated with the clinicopathological variables, enabling us to discriminate a subset of patients at higher risk of progression within the Stage, Size, Grade and Necrosis score (SSIGN) risk groups, pT and ISUP grade. In summary, a gene expression-based prognostic signature was successfully developed providing a more precise assessment of the individual risk of progression.

Indexed as

biomarkersclear-cell renal cell carcinomadisease progressiongene expressionprognostic factorsRNA sequencing

Identifiers

PMID35954418
PMCPMC9367562
OpenAlexW4289313499

What OpenQuestion holds

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LicenceCC BY
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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.