Evidence map›Paper›PMID 38844723›Full record

ArticleJournal of cancer research and clinical oncology2024

DIAPH2 gene polymorphisms and laryngeal cancer risk in men.

Edyta Cichocka, Sylwia Górczyńska-Kosiorz, Maciej Misiołek, Wojciech Ścierski, Anna Koniewska, Grażyna Stryjewska-Makuch, Janusz Gumprecht

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Article in Journal of cancer research and clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Edyta CichockaMedical University of Silesia, Katowice, Poland. ecichocka@sum.edu.pl.
Sylwia Górczyńska-KosiorzMedical University of Silesia, Katowice, Poland.
Maciej MisiołekMedical University of Silesia, Katowice, Poland.
Wojciech ŚcierskiMedical University of Silesia, Katowice, Poland.
Anna KoniewskaMedical University of Silesia, Katowice, Poland.
Grażyna Stryjewska-MakuchMedical University of Silesia, Katowice, Poland.
Janusz GumprechtMedical University of Silesia, Katowice, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe DIAPH2 gene is one of the genes commonly associated with laryngeal squamous cell carcinoma (LSCC). In our study, we considered the four polymorphisms of this gene, i.e. rs5920828, rs4322175, rs12851931 and rs5921830 as potential genetic risk factors for LSCC.

methodsWe determined the genotyping of the genetic variants of DIAPH2 in 230 male patients with histologically confirmed LSCC compared to the European population. Demographic and environmental exposure data of each subject were examined. To conduct the genetic tests, extraction of total DNA was performed. We genotyped all four variants in each patient and determined their frequencies.

resultsIn the case of the rs12851931 polymorphism in the DIAPH2 gene, a significant difference was observed in the distribution of the T stage depending on the polymorphism. Heterozygotes were more often associated with T2 stage, while homozygotes were more likely to have higher tumor stages. The rs12851931 homozygotes of DIAPH2 were statistically significantly more prevalent in smokers. The results suggested that rs12851931 polymorphism in DIAPH2 could increase the onset risk of LSCC.

conclusionsOur results provide further information on the role of the DIAPH2 gene in the pathogenesis of LSCC.

Indexed as

ForminsGenetic Predisposition to DiseaseLaryngeal NeoplasmsPolymorphism, Single NucleotideAdultAgedCarcinoma, Squamous CellGenotypeHumansMaleMiddle AgedRisk FactorsDIAPH2 protein, humanForminsDIAPH2 gene polymorphismsGenetic factorLaryngeal cancer risk

Identifiers

PMID38844723
PMCPMC11156712

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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.