Evidence map›Paper›PMID 41029134›Full record

Observational studyMedicine2025

Prognostic difference of molecular subtypes in non-muscle invasive bladder cancer.

Mahmut Naci Çatal, İlker Akarken, Yelda Dere, Hasan Deliktaş, Hüseyin Tarhan, Hayrettin Şahin

Abstract readObservational Study
In one paragraph

Observational study in Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Mahmut Naci ÇatalDepartment of Urology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.
İlker AkarkenDepartment of Urology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.
Yelda DereDepartment of Pathology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.ORCID 0000-0003-0238-2236
Hasan DeliktaşDepartment of Urology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.
Hüseyin TarhanDepartment of Urology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.
Hayrettin ŞahinDepartment of Urology, Muğla Sitki Koçman University Faculty of Medicine, Muğla, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, 2 molecular types have been defined in urothelial carcinoma, as luminal and basal. The molecular subtyping is generally based on genetic studies in non-muscle invasive bladder cancer (NMIBC) however the studies with immunohistochemical reflection of this subtyping in NMIBC is limited. In our study, we aimed to use GATA3 and keratin 5/6 for subtyping of NMIBC, and to investigate the follow-up results. Materials and methods: Patients who underwent transurethral resection for the first time and whose final diagnosis was reported as NMIBC were prospectively included. A block representing the tumor was stained with GATA3 and keratin 5/6.The relationships between the subtypes and demographic data, recurrence rates, and time to recurrence were evaluated. A total of 100 patients diagnosed with NMIBC were included. The keratin 5/6 negativity was 64% and all of these patients were GATA3 positive. The keratin 5/6 positivity was 36%. None of the age, tumor size, lamina propria invasion, keratin 5/6 and GATA3 positivity were significant for predicting the risk of recurrence. The mean time to recurrence was 283 days and 332 days in the keratin 5/6 positive and negative group, respectively but the relation was not statistically significant. Molecular classification is difficult due to technical reasons, but it can be performed with GATA3 and keratin 5/6 by immunohistochemistry. New studies are needed to determine the clinical differences and to specialize the management of bladder tumors.

Indexed as

GATA3 Transcription FactorUrinary Bladder NeoplasmsAgedAged, 80 and overBiomarkers, TumorFemaleHumansImmunohistochemistryKeratin-5Keratin-6MaleMiddle AgedNeoplasm InvasivenessNeoplasm Recurrence, LocalNon-Muscle Invasive Bladder NeoplasmsPrognosisBiomarkers, TumorGATA3 protein, humanGATA3 Transcription FactorKeratin-5Keratin-6bladder cancerGATA3keratin 5/6molecular subtype

Identifiers

PMID41029134
PMCPMC13592937

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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.