Evidence map›Paper›PMID 41773809›Full record

ArticleAPMIS : acta pathologica, microbiologica, et immunologica Scandinavica2026

Analysis of Human miRNA Derived From Bladder Epithelial Cells Infected With Uropathogenic Escherichia coli.

Katarina Persson, Isak Demirel, Ignacio Rangel, Robert Kruse

Abstract read
In one paragraph

Article in APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 2026. 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

4 authors.

Katarina PerssonSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Isak DemirelSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID https://orcid.org/0009-0002-0420-7538
Ignacio RangelSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Robert KruseDepartment of Clinical Research Laboratory, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Funding

Faculty of Medicine and Health at Örebro UniversityNyckelfonden
6 · The paper itself

Abstract

MicroRNAs (miRNAs) have been shown to regulate many cellular processes and to play a role in host-pathogen interactions. However, the role of miRNA in urinary tract infection (UTI) remains unclear. The aim of this study was to analyze and compare miRNAs from supernatants of human bladder epithelial cells infected with ESBL-producing (ESBL019) and non-ESBL-producing (CFT073) uropathogenic E. coli (UPEC) strains and to identify miRNA target genes in human cells and uropathogenic bacteria. In total, 402 unique miRNAs were found. The statistical analysis showed differential expression of 30 miRNAs from bladder cells stimulated with ESBL019, while stimulation with CFT073 did not show any significantly expressed miRNAs when compared to unstimulated controls. The 30 differentially expressed miRNAs in ESBL019 stimulated cells showed 747 predicted individual human gene targets. KEGG and REACTOME pathways showed enrichments in pathways mainly connected to immune regulation and stress responses. Of the 30 differentially expressed host miRNAs, nine miRNAs were found to interact with predictive targets of the whole genome from the multi-resistant, ESBL-producing UPEC strain EC958. This study shows that ESBL019-infected bladder epithelial cells release miRNAs with predictive targets in both human and bacterial genes, although their role in UTI cross-species interactions remains to be clarified.

Indexed as

Epithelial CellsEscherichia coli InfectionsMicroRNAsUrinary BladderUrinary Tract InfectionsUropathogenic Escherichia coliCell LineGene Expression ProfilingHost-Pathogen InteractionsHumansMicroRNAsESBLmiRNAUPECurinary bladderurinary tract infection

Identifiers

PMID41773809
PMCPMC12955519

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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.