Evidence map›Paper›PMID 38158432›Full record

ArticleMolecular biology reports2023

Unveiling the etiological impact of GST-M1, GST-T1, and P53 genotypic variations on brain carcinogenesis.

Onur Dirican, Pınar Kaygın, Serpil Oğuztüzün, Abbas Ali Husseini, Sezen Yılmaz Sarıaltın, Can Yılmaz, Nihan Ünlü, Yusuf İzci

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Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

8 authors at 5 institutions in 1 country.

Onur DiricanDepartment of Pathology Laboratory Techniques, Vocational School of Health Services, Istanbul Gelişim University, Istanbul, Turkey. odirican@gelisim.edu.tr.
Pınar KaygınDepartment of Biology, Faculty of Art and Science, University of Kırıkkale, Kırıkkale, Turkey.
Serpil OğuztüzünDepartment of Biology, Faculty of Art and Science, University of Kırıkkale, Kırıkkale, Turkey.
Abbas Ali HusseiniLife Science and Biomedical Engineering Application and Research Center, Istanbul Gelisim University, Istanbul, Turkey.
Sezen Yılmaz SarıaltınDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, University of Ankara, Ankara, Turkey.
Can YılmazDepartment of Molecular Biology and Genetics, Faculty of Art and Science, University of Yüzüncü Yıl, Van, Turkey.
Nihan ÜnlüDepartment of Medical Services and Techniques, Vocational School of Health Sciences, Istanbul Gelisim University, Istanbul, Turkey.
Yusuf İzciDepartment of Neurosurgery, Gülhane Training and Research Hospital, University of Health Sciences, Ankara, Turkey.
İstanbul Gelişim Üniversitesi · TRKırıkkale University · TRAnkara University · TRSağlık Bilimleri Üniversitesi · TRVan Yüzüncü Yıl Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFunctional variants of glutathione-S-transferase (GST)-M1, GST-T1, p53 might modulate brain cancer risk by altering the rate of metabolism and clearance of carcinogens from the brain tissue. In this study, the role of GST-M1, GST-T1, p53 polymorphisms on brain tumor was investigated. METHODS AND

resultsBrain tumor tissues of 143 patients were obtained from the Gulhane Training and Research Hospital, Department of Neurosurgery between 2019 and 2020. In the xenobiotic mechanism, the null allele frequency in the GST-T1, GST-M1 gene regions of Phase II enzymes by qPCR method were investigated. Single nucleotide polymorphism encoding Arg/Pro conversion in the p53 gene region was analyzed in 120 cases by sequence analysis method. The data were analyzed statistically with patient's demographic and clinical data. GST-M1, GST-T1, p53 genotypes of the patient group were determined. The most frequent genotype was null genotype (0/0) for GST-M1 (χ

conclusionThe null allele frequency encountered in the GST-M1, GST-T1 gene regions is consistent with the rates in the gene pool called Caucasian in the literature. GST-M1 gene polymorphism may play a crucial role in brain carcinogenesis in Turkish patients. This study based on clinical data is thought to help to understand the important epidemiological features of brain tumors.

Indexed as

Brain NeoplasmsTumor Suppressor Protein p53BrainCarcinogenesisCase-Control StudiesCodonGenetic Predisposition to DiseaseGenotypeGlutathione TransferaseHumansPolymorphism, Single NucleotideCodonGlutathione TransferaseTumor Suppressor Protein p53Brain tumorsGST-M1GST-T1p53Polymorphism

Identifiers

PMID38158432
OpenAlexW4390393905

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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.