Evidence map›Paper›PMID 39336817›Full record

ReviewGenes2024

The Role of Single Nucleotide Polymorphisms in MicroRNA Genes in Head and Neck Squamous Cell Carcinomas: Susceptibility and Prognosis.

Elżbieta Szmida, Dorota Butkiewicz, Paweł Karpiński, Tomasz Rutkowski, Małgorzata Oczko-Wojciechowska, Maria Małgorzata Sąsiadek

Abstract readReview
In one paragraph

Review in Genes, 2024. 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. Associations of combined lifestyle and genetic risk with incident head and neck cancer: a prospective study in the UK Biobank.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
    Article
  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

6 authors.

Elżbieta SzmidaDepartment of Genetics, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Dorota ButkiewiczCenter for Translational Research and Molecular Biology of Cancer, Maria Skłodowska-Curie National Research Institute of Oncology Gliwice Branch, 44-102 Gliwice, Poland.ORCID 0000-0002-4043-3789
Paweł KarpińskiDepartment of Genetics, Wroclaw Medical University, 50-367 Wroclaw, Poland.ORCID 0000-0003-3885-694X
Tomasz RutkowskiRadiotherapy Department, Maria Skłodowska-Curie National Research Institute of Oncology Gliwice Branch, 44-102 Gliwice, Poland.ORCID 0000-0003-2735-5664
Małgorzata Oczko-WojciechowskaDepartment of Clinical and Molecular Genetics, Maria Skłodowska-Curie National Research Institute of Oncology Gliwice Branch, 44-102 Gliwice, Poland.ORCID 0000-0002-8989-0075
Maria Małgorzata SąsiadekDepartment of Genetics, Wroclaw Medical University, 50-367 Wroclaw, Poland.ORCID 0000-0002-7599-7074

Funding

National Science Centre 2016/23/B/NZ5/03470Wroclaw Medical University SUBK.A290.21.019; SUBK.A290.22.058
6 · The paper itself

Abstract

backgroundHead and neck squamous cell carcinoma (HNSCC) is one of the most prevalent cancers worldwide. The identification of molecular alterations adding to the individual risk of HNSCC development and progression is one of the most important challenges in studies on cancer genetics. MicroRNAs (miRNAs), which belong to the group of important post-transcriptional regulators of human gene expression, seem to be valuable options for consideration as key modifiers of individual cancer risk, and therefore may be helpful in predicting inter-individual differences in cancer risk, response to treatment and prognosis.

methodsThere have not been many studies focused on the relationship between miRNA variants and HNSCC published in PubMed within the last 15 years. We found and analyzed 30 reviews, meta-analyses and research papers and revealed 14 SNPs which have been reported as significant in the context of HNSCC susceptibility and/or prognosis.

resultsThese 14 SNPs were located in 13 separate miRNAs. Among them, four were the most frequently studied (miRNA-146, -196, -149 and -499) and have been shown to have the greatest impact on the course of HNSCC. However, the presented results have been conflicting.

conclusionsIt must be concluded that, despite the years of studies, there are no conclusive reports demonstrating a significant role of SNPs in miRNAs in the context of the susceptibility to HNSCC or its prognosis.

Indexed as

Genetic Predisposition to DiseaseHead and Neck NeoplasmsMicroRNAsPolymorphism, Single NucleotideSquamous Cell Carcinoma of Head and NeckCarcinoma, Squamous CellGene Expression Regulation, NeoplasticHumansPrognosisMicroRNAsbiomarkerscancer riskhead and neck cancerHNSCCmiRNApolymorphismsprognosisSNPs

Identifiers

PMID39336817
PMCPMC11431317

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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.