Evidence map›Paper›PMID 36593286›Full record

ArticleScientific reports2023

CDCP1 expression is frequently increased in aggressive urothelial carcinoma and promotes urothelial tumor progression.

Miriam Saponaro, Sina Flottmann, Markus Eckstein, Oliver Hommerding, Niklas Klümper, Dillon Corvino, Sana Hosni, Anja Schmidt, Nicolas Mönig, Doris Schmidt and 8 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 2 institutions in 2 countries.

Miriam Saponaro *Department of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Sina Flottmann *Department of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Markus EcksteinInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Oliver HommerdingInstitute of Pathology, University Medical Center Bonn (UKB), Bonn, Germany.
Niklas KlümperDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Dillon CorvinoInstitute of Experimental Oncology, University Medical Center Bonn (UKB), Bonn, Germany.
Sana HosniDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Anja SchmidtDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Nicolas MönigDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Doris SchmidtDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Jörg EllingerDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Marieta TomaInstitute of Pathology, University Medical Center Bonn (UKB), Bonn, Germany.
Glen KristiansenInstitute of Pathology, University Medical Center Bonn (UKB), Bonn, Germany.
Tobias BaldInstitute of Experimental Oncology, University Medical Center Bonn (UKB), Bonn, Germany.
Andrea AlimontiInstitute of Oncology Research, Università Della Svizzera Italiana, Bellinzona, Switzerland.
Manuel RitterDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany.
Michael HölzelInstitute of Experimental Oncology, University Medical Center Bonn (UKB), Bonn, Germany.
Abdullah AlajatiDepartment of Urology and Pediatric Urology, University Medical Center Bonn (UKB), Venusberg-Campus 1, 53127, Bonn, Germany. abdullah.alajati@ukbonn.de.
Institute of Oncology Research · CHUniversitätsklinikum Erlangen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of patients with advanced urothelial carcinoma (UC) remains poor and improving treatment continues to be a major medical need. CUB domain containing protein 1 (CDCP1) is a known oncogene in various types of solid cancers and its overexpression is associated with impaired prognosis. However, its role in UC remains undetermined. Here we assessed the clinical relevance of CDCP1 in two cohorts of UC at different stages of the disease. Immunohistochemistry showed that CDCP1 is highly expressed in advanced UC, which significantly correlates with shorter overall survival. Importantly, the basal/squamous UC subtype showed significantly enriched CDCP1 at the mRNA and protein levels. The functional role of CDCP1 overexpression was assessed taking advantage of ex vivo organoids derived from the CDCP1

Indexed as

Carcinoma, Transitional CellCell Adhesion MoleculesUrinary Bladder NeoplasmsUrologic NeoplasmsAnimalsAntigens, NeoplasmCell Line, TumorHumansMiceNeoplasm ProteinsAntigens, NeoplasmCDCP1 protein, humanCDCP1 protein, mouseCell Adhesion MoleculesNeoplasm Proteins

Identifiers

PMID36593286
PMCPMC9807563
OpenAlexW4313478145

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.