Evidence map›Paper›PMID 38914847›Full record

ArticleBiochemical genetics2025

Exploring of miR-155-5p, miR-181b-5p, and miR-454-3p Expressions in Circulating Cell-Free RNA: Insights from Peripheral Blood of Uveal Malignant Melanoma Patients.

Hassani Masoumeh, Doğan Tunay, Ödemiş Akdeniz Demet, Tuncer Samuray, Yazıcı Hülya

Abstract read
In one paragraph

Article in Biochemical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

5 authors.

Hassani MasoumehCancer Genetics Division, Oncology Institute, İstanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye.ORCID http://orcid.org/0000-0001-8976-4450
Doğan TunayCancer Genetics Division, Oncology Institute, İstanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye.ORCID http://orcid.org/0000-0001-5281-7360
Ödemiş Akdeniz DemetCancer Genetics Division, Oncology Institute, İstanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye.ORCID http://orcid.org/0000-0002-2271-8481
Tuncer SamurayDepartment of Eye Diseases, Faculty of Medicine, İstanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye.ORCID http://orcid.org/0000-0001-7491-8613
Yazıcı HülyaCancer Genetics Division, Oncology Institute, İstanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye. hulyayazici67@gmail.com.ORCID http://orcid.org/0000-0002-8919-0482

Funding

This study was funded by the Scientific Research Projects Coordination Unit of Istanbul University Grant number: TDK-2019-35336.
6 · The paper itself

Abstract

The identification of novel non-invasive biomarkers is imperative for the early diagnosis and monitoring of malignant melanoma. The objective of this study is to examine the expression levels of miR-155-5p, miR-181b-5p, and miR-454-3p in circulating cell-free RNA obtained from plasma samples of the 72 uveal malignant melanoma patients and to compare these levels with those of 72 healthy controls. The analysis showed that the expression level of the miR-181b-5p has increased 9.25 fold, and expression level of miR-155-5p has increased 6.67 fold, and miR-454-3p expression level has increased 4.14 fold in the patient group compared with the levels in the healthy control group (p = 0.005). It was found that the high expression levels of the three miRNAs were statistically significant in patients compared with in the healthy control group. The statistical evaluations between miRNA expression levels and clinical data showed that miR-155-5p had significant association with radiation therapy (p = 0.040), and miR-454-3p showed a significant association with smoking and alcohol use respectively (p = 0.009, and p = 0.026). The significantly elevated expression levels of miR-181b-5p, miR-155-5p, and miR-454-3p in the circulating cell-free RNA of plasma from uveal melanoma patients, in comparison to those in the healthy control group, suggest the potential usefulness of these biomarkers for both early diagnosis and disease monitoring. However, more extensive and future studies are needed to use these molecules in early diagnosis and disease monitoring.

Indexed as

Biomarkers, TumorCell-Free Nucleic AcidsMelanomaMicroRNAsUveal NeoplasmsAdultAgedCase-Control StudiesFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedUveal MelanomaBiomarkers, TumorCell-Free Nucleic AcidsMicroRNAsMIRN155 microRNA, humanMIrn181 microRNA, humanCirculating cell free miRNAmiR-155-5pmiR-181b-5pmiR-454-3pPlasmaUveal Melanoma

Identifiers

PMID38914847
PMCPMC12271267

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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 Socratic graph.