Evidence map›Paper›PMID 28488172›Full record

ArticleVirchows Archiv : an international journal of pathology2017

Clear cell renal cell carcinoma: a comparative study of histological and chromosomal characteristics between primary tumors and their corresponding metastases.

Julien Dagher, Solène-Florence Kammerer-Jacquet, Frédéric Dugay, Marion Beaumont, Alexandra Lespagnol, Laurence Cornevin, Grégory Verhoest, Karim Bensalah, Nathalie Rioux-Leclercq, Marc-Antoine Belaud-Rotureau

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Development and Identification of a Nomogram Prognostic Model for Patients with Primary Clear Cell Carcinoma of the Liver.Medical science monitor : international medical journal of experimental and clinical research · 2020
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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

10 authors at 5 institutions in 1 country.

Julien DagherIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France.
Solène-Florence Kammerer-JacquetIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France.
Frédéric DugayIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France.
Marion BeaumontIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France.
Alexandra LespagnolService de Génétique Moléculaire et Génomique, Université de Rennes 1, 35042, Rennes, France.
Laurence CornevinService de Cytogénétique et Biologie Cellulaire, Université de Rennes 1, 35042, Rennes, France.
Grégory VerhoestService d'Urologie, Université de Rennes 1, 35042, Rennes, France.
Karim BensalahService d'Urologie, Université de Rennes 1, 35042, Rennes, France.
Nathalie Rioux-LeclercqIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France.
Marc-Antoine Belaud-RotureauIRSET INSERM UMR 1085, Faculté de Médecine de Rennes 1, 35043, Rennes, France. marc-antoine.belaud-rotureau@chu-rennes.fr.
Université de Rennes · FRCentre Hospitalier Universitaire de Rennes · FRInstitut de Recherche en Santé, Environnement et Travail · FRInserm · FRLaboratoire de Génétique Cellulaire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) has a poor prognosis with a 50% risk of metastases. Little is known about the phenotypic and molecular profiles of metastases regarding their corresponding primary tumors. This study aimed to screen phenotypic and genotypic differences between metastases and their corresponding primary tumors. We selected four cases with available frozen material. The histological, immunohistochemical (VEGFA, CD31, SMA, Ki67, p53, PAR-3), FISH (VHL gene), next-generation sequencing (VHL and c-MET genes), multiplex ligation-dependent probe amplification, and array-(comparative genomic hybridization) CGH analyses were realized. Metastases were nodal, hepatic (synchronous), adrenal, and pulmonary (metachronous). High-grade tumor cells were significantly more frequent in metastases (p = 0.019). Metastases and high-grade zones of primary tumors shared similar characteristics compared to low-grade zones: a lower microscopic vascular density (43.5 vs 382.5 vessels/mm

Indexed as

AgedCarcinoma, Renal CellComparative Genomic HybridizationHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryIn Situ Hybridization, FluorescenceKidney NeoplasmsMaleMiddle AgedMultiplex Polymerase Chain ReactionMutationNeoplasm MetastasisOligonucleotide Array Sequence AnalysisProto-Oncogene Proteins c-metVon Hippel-Lindau Tumor Suppressor ProteinMET protein, humanProto-Oncogene Proteins c-metVHL protein, humanVon Hippel-Lindau Tumor Suppressor ProteinCGHChromosomeClear cell renal cell carcinomaMetastasis

Identifiers

PMID28488172
OpenAlexW2613031934

What OpenQuestion holds

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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.