Evidence map›Paper›PMID 41050687›Full record

SynthesisFrontiers in immunology2025

The miRNA-immune axis in bladder cancer: systematic evidence for a new era of immunotherapy precision.

Daniel-Vasile Dulf, Gloria Ravegnini, Federico Manuel Giorgi, Anamaria Larisa Burnar, Francesca Gorini, Antonio De Leo, Harisa Luţichievici, Constantin-Lucian Opriţa, Cezar-Nicolae Todiruţ, Tudor-Eliade Ciuleanu and 1 more

Abstract readSystematic Review
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Daniel-Vasile Dulf10th Department - Oncology, "Iuliu Haţieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Gloria RavegniniDepartment of Pharmacy and Biotechnology (FABIT), University of Bologna, Bologna, Italy.
Federico Manuel GiorgiDepartment of Pharmacy and Biotechnology (FABIT), University of Bologna, Bologna, Italy.
Anamaria Larisa BurnarInstitute of Oncology "Prof. Dr. Ion Chiricuţă", Cluj-Napoca, Romania.
Francesca GoriniDepartment of Pharmacy and Biotechnology (FABIT), University of Bologna, Bologna, Italy.
Antonio De LeoSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Harisa LuţichieviciFaculty of Medicine, University of Medicine and Pharmacy "Iuliu Haţieganu", Cluj-Napoca, Romania.
Constantin-Lucian OpriţaFaculty of Medicine, University of Medicine and Pharmacy "Iuliu Haţieganu", Cluj-Napoca, Romania.
Cezar-Nicolae TodiruţFaculty of Medicine, University of Medicine and Pharmacy "Iuliu Haţieganu", Cluj-Napoca, Romania.
Tudor-Eliade Ciuleanu10th Department - Oncology, "Iuliu Haţieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Camelia Alexandra CoadăDepartment of Morpho-functional Sciences, University of Medicine and Pharmacy "Iuliu Haţieganu", Cluj-Napoca, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bladder cancer (BC) is a complex disease with patients showing widely variable responses to treatment. While immunotherapy has recently emerged as a promising alternative to the standard platinum-based chemotherapy, especially for platinum-resistant tumors, clinicians still lack reliable biomarkers to predict which patients will truly benefit from immunotherapy. Aim: This systematic review aimed to explore whether miRNAs could help decode the immune landscape of BC and serve as predictive biomarkers for immunotherapy response. Methods: A total of 3,272 articles were systematically screened on medical databases and narrowed down to 37 studies that examined the relationship between miRNAs, immune cell infiltration, and patient outcomes in BC. To further strengthen and validate our findings, we analyzed large-scale genomic data from The Cancer Genome Atlas (TCGA-BLCA). Results: A total of 104 different miRNAs appeared to shape the BC immune microenvironment. Some studies also linked miRNA expression with clinical outcomes such as BCG therapy response and prognosis, while others dissected the molecular pathways. Further analyses established miR-155, miR-142, and miR-146b as key factors for CD4 Conclusion: miRNAs are emerging as powerful regulators of the immune microenvironment of BC. However, despite growing evidence, to date, no studies have directly explored miRNA profiles in driving immunotherapeutic decisions. Our findings highlight the need for prospective studies to translate these molecular insights into personalized treatment strategies.

Indexed as

Biomarkers, TumorImmunotherapyMicroRNAsUrinary Bladder NeoplasmsGene Expression Regulation, NeoplasticHumansPrecision MedicinePrognosisTumor MicroenvironmentBiomarkers, TumorMicroRNAsimmune checkpoint inhibitorimmunotherapymicroRNAPD-L1personalized therapyprognosistumor immune infiltrationurothelial carcinoma

Identifiers

PMID41050687
PMCPMC12491296

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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.