Evidence map›Paper›PMID 41569501›Full record

ArticleCell biochemistry and biophysics2026

The Role of miR-155-5p, PIK3K/AKT/HIF-1α Signaling Pathway, and Oxidative Stress in Nasal Polyp Formation: A Molecular Insight into Potential Therapeutic Targets.

Muhammet Yusuf Tepebaşi, Yusuf Çağdaş Kumbul, Halil İbrahim Büyükbayram, Hasan Yasan, Melda Şahin

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Article in Cell biochemistry and biophysics, 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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0cells of the map it votes in
0citing papers in PubMed
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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

5 authors.

Muhammet Yusuf TepebaşiDepartment of Medical Genetics, University of Süleyman Demirel, Isparta, Turkey. muhammettepebasi@sdu.edu.tr.ORCID http://orcid.org/0000-0002-1087-4874
Yusuf Çağdaş KumbulDepartment of Otorhinolaryngology, University of Süleyman Demirel, Isparta, Turkey.ORCID http://orcid.org/0000-0002-0713-2933
Halil İbrahim BüyükbayramDepartment of Medical Biochemistry, University of Süleyman Demirel, Isparta, Turkey.ORCID http://orcid.org/0000-0003-0560-042X
Hasan YasanDepartment of Otorhinolaryngology, University of Süleyman Demirel, Isparta, Turkey.ORCID http://orcid.org/0000-0002-5470-6784
Melda ŞahinSüleyman Demirel University, Institute of Natural and Applied Sciences, Department of Bioengineering, Isparta, Turkey.ORCID http://orcid.org/0000-0001-9207-6931

Funding

Süleyman Demirel Üniversitesi TSG-2022-8983
6 · The paper itself

Abstract

Nasal polyps (NPs) are benign, inflammatory soft tissue growths in the nasal and paranasal sinus passages that are closely associated with chronic rhinosinusitis (CRS), which has a major influence on patients’ quality of life. This study aimed to investigate the role of miR-155-5p, its target genes, and oxidative stress in the molecular mechanisms driving NP formation. A total of 133 patients, including those with NPs (n = 65) and middle concha bullosa (n = 68), were evaluated via endoscopic examination and computed tomography. Tissue samples were stained with hematoxylin and eosin to examine structural alterations, and TUNEL labeling was used to detect apoptotic cells. Quantitative RT-qPCR was utilized to quantify miR-155-5p and its target genes (PI3K, HIF-1α, IL-6, and Bcl-2). Oxidative stress markers such as TOS (total oxidant status), SOD (superoxide dismutase) GPx (glutathione peroxidase), and TAS (total antioxidant status) were measured spectrophotometrically, and the oxidative stress index (OSI) was derived to offer an overall oxidative stress measure. Histopathological analysis revealed significant eosinophil infiltration and basement membrane thickening in NP tissues compared to concha bullosa samples. Apoptosis rates were notably higher in concha bullosa tissues. NP tissues showed an upregulation of miR-155-5p and its target genes (PI3K, HIF-1α, IL-6, and Bcl-2). Additionally, NP samples showed an increase in oxidative stress, which was shown by higher TOS and OSI values and lower TAS, suggesting that oxidative imbalance may play a role in NP pathophysiology. Our results suggest that the PI3K/AKT/HIF-1α signaling pathway and miR-155-5p are important for NP production. The observed oxidative stress suggests that targeting both oxidative pathways and miR-155-5p-associated signaling could be beneficial in developing future therapeutic strategies. This study provides novel insights into the molecular underpinnings of NP formation, identifying potential therapeutic targets for improved clinical management.

Indexed as

MicroRNAsNasal PolypsOxidative StressPhosphatidylinositol 3-KinasesSignal TransductionAdultApoptosisFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMiddle AgedProto-Oncogene Proteins c-aktHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN155 microRNA, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktHIF-1αmiR-155-5pNasal polypOxidative stressPI3K, akt

Identifiers

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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.