Evidence map›Paper›PMID 30019121›Full record

ArticlePathology oncology research : POR2020

Nuclear Localization of Robo is Associated with Better Survival in Bladder Cancer.

Ulrich Krafft, Henning Reis, Marc Ingenwerth, Ilona Kovalszky, Markus Becker, Christian Niedworok, Christopher Darr, Péter Nyirády, Boris Hadaschik, Tibor Szarvas

Abstract read
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In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
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 2 institutions in 2 countries.

Ulrich KrafftDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany.
Henning ReisInstitute of Pathology, Faculty of Medicine, University Duisburg-Essen, Essen, Germany.
Marc IngenwerthInstitute of Pathology, Faculty of Medicine, University Duisburg-Essen, Essen, Germany.
Ilona Kovalszky1st Institute of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Markus BeckerDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany.
Christian NiedworokDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany.
Christopher DarrDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany.
Péter NyirádyDepartment of Urology, Semmelweis University, Üllöi út 78/b, Budapest, 1082, Hungary.
Boris HadaschikDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany.
Tibor SzarvasDepartment of Urology, Faculty of Medicine, University Duisburg-Essen, Hufelandstr 55, 45147, Essen, Germany. sztibusz@gmail.com.
University of Duisburg-Essen · DESemmelweis University · HU

Funding

Magyar Tudományos Akadémia BolyaiNKFIH PD 115616
6 · The paper itself

Abstract

The Slit-Robo pathway has shown to be altered in several malignant diseases. However, its role in bladder cancer is poorly understood. Therefore, we aimed to assess the tissue expression of Robo1 and Robo4 as well as their ligand Slit2 in different stages of bladder cancer to explore possible changes of Slit-Robo signalling during the progression of bladder cancer. Robo1, Robo4 and Slit2 gene expressions were analyzed in 92 frozen bladder cancer tissue samples by using reverse transcription quantitative real-time PCR. Immunohistochemical analyses were performed on 149 formalin-fixed and paraffin-embedded bladder cancer tissue samples. Results were correlated with the clinical and follow-up data by performing both univariable and multivariable analyses. Robo1 and Robo4 nuclear staining intensitiy was significantly higher in low stage and low grade bladder cancer. Elevated Robo1 nuclear staining was associated with better disease-specific survival (DSS) (p = 0.045). Similarly, stronger Robo4 nuclear staining tended to be associated with longer DSS (p = 0.061). We found higher Robo1 and Slit2 gene expression levels in advanced stages of bladder cancer (p = 0.007 and p < 0.001). High Slit2 gene expression was correlated with significantly shorter DSS (p < 0.005), while Robo1 and Robo4 gene expressions were not associated with patients' prognosis. Our results demonstrate that the nuclear expression of Robo1 and Robo4 is associated with a favourable prognosis suggesting that its translocation into the nucleus represent a posttranslational regulation process which may exhibit an antitumor effect in bladder cancer.

Indexed as

AgedBiomarkers, TumorCell NucleusFemaleHumansIntercellular Signaling Peptides and ProteinsMaleMiddle AgedNerve Tissue ProteinsPrognosisReceptors, Cell SurfaceReceptors, ImmunologicRoundabout ProteinsSlit Homolog 2 ProteinUrinary Bladder NeoplasmsBiomarkers, TumorIntercellular Signaling Peptides and ProteinsNerve Tissue ProteinsReceptors, Cell SurfaceReceptors, ImmunologicROBO4 protein, humanRoundabout ProteinsSlit Homolog 2 ProteinAngiogenesisBladder CancerNuclear translocationPrognosisRobo1Robo4Slit2

Identifiers

PMID30019121
OpenAlexW2884830167

What OpenQuestion holds

Textmetadata
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.