Evidence map›Paper›PMID 42334004›Full record

ArticleThe journal of pathology. Clinical research2026

Ectonucleotidases CD39 and CD73 expression levels are independent and inverse predictors of survival in muscle-invasive bladder cancer.

Stephan Ledderose, Julia Schwenke, Lennert Eismann, Severin Rodler, Martina Rudelius, Carola Ledderose

Abstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2026. 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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Stephan LedderoseInstitute of Pathology, Ludwig Maximilian University Munich, Munich, Germany.ORCID https://orcid.org/0000-0001-7313-2088
Julia SchwenkeInstitute of Pathology, Ludwig Maximilian University Munich, Munich, Germany.
Lennert EismannDepartment of Urology, Ludwig Maximilian University Munich, Munich, Germany.
Severin RodlerDepartment of Urology, University Hospital of Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Martina RudeliusInstitute of Pathology, Ludwig Maximilian University Munich, Munich, Germany.
Carola LedderoseDepartment of Surgery, University of California San Diego Health, San Diego, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer is one of the leading causes of cancer-related mortality worldwide. Long-term survival is particularly poor in patients with muscle-invasive bladder cancer (MIBC). Modulation of purinergic signaling through the ectonucleotidases CD39 and CD73 has emerged as a promising therapeutic strategy in cancer medicine. Altered expression patterns of these molecules have been linked to prognosis in various malignancies. In this study, we assessed the value of CD39 and CD73 expression as prognostic markers and potential therapeutic targets in MIBC. CD39 and CD73 expression was determined by immunohistochemistry using tissue microarrays from 180 patients with MIBC. Associations between tumoral and stromal expression and clinicopathological variables, including overall survival (OS), tumor-specific survival (TSS) and disease-free survival (DFS), were analyzed. Tumor cells did not express CD39. High stromal CD39 expression was significantly associated with a lower T category and UICC stage as well as prolonged median OS, TSS, and DFS. High CD73 expression by tumor cells was significantly associated with poorer OS and TSS. Stromal CD73 expression was not significantly correlated with survival outcomes. Our findings indicate distinct and compartment-specific roles for CD39 and CD73 in MIBC. They suggest that high CD73 expression in tumor cells and low CD39 expression in stromal cells are negative prognostic indicators and potential therapeutic targets in MIBC.

Indexed as

5'-NucleotidaseAntigens, CDApyraseBiomarkers, TumorUrinary Bladder NeoplasmsAdultAgedAged, 80 and overDisease-Free SurvivalFemaleGPI-Linked ProteinsHumansImmunohistochemistryKaplan-Meier EstimateMaleMiddle Aged5'-NucleotidaseAntigens, CDApyraseBiomarkers, TumorGPI-Linked ProteinsNT5E protein, humanbiomarkerbladder cancerCD39CD73prognosispurinergic signalingtumor microenvironment

Identifiers

PMID42334004
PMCPMC13288156

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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.