Evidence map›Paper›PMID 28220295›Full record

ArticleJournal of gastrointestinal cancer2018

DNMT3B -579 G>T Promoter Polymorphism and the Risk of Gastric Cancer in the West of Iran.

Kulsom Ahmadi, Azam Soleimani, Shiva Irani, Aliasghar Kiani, Kourosh Ghanadi, Zahra Noormohamadi, Foroozan Sakinejad

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In one paragraph

Article in Journal of gastrointestinal cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Monitoring of the choline/lipid ratio byLasers in medical science · 2022
    Article
  3. Article
  4. Epidemiologic Study of Gastric Cancer in Iran: A Systematic Review.Clinical and experimental gastroenterology · 2020
    Review
  5. 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

7 authors.

Kulsom AhmadiLorestan University of Medical Sciences, Khorramabad, Iran.
Azam SoleimaniRazi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran. asoleymani12@gmail.com.
Shiva IraniDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Aliasghar KianiLorestan University of Medical Sciences, Khorramabad, Iran.
Kourosh GhanadiRazi Herbal Medicines Research Center and Department of Internal Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Zahra NoormohamadiDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Foroozan SakinejadFatemeh Zahra laboratory, Khorramabad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany studies have suggested that modulation of DNMT3B function caused by single nucleotide polymorphisms of the DNMT3B promoter region may underlie the susceptibility to various cancers such as tumors of the digestive system. The aim of this study was to investigate the effect of -579 G>T polymorphism in the promoter of the DNMT3B gene on risk of gastric cancer in a population from West Iran. PATIENTS AND

methodsWe conducted a case-control study in 100 gastric cancer patients and 112 cancer-free controls to assess the correlation between DNMT3B -579 G>T (rs1569686) polymorphism and the risk of gastric cancer. Detection of genotypes of DNMT3B G39179T polymorphism was analyzed by PCR-RFLP.

resultsThere was no significant difference in the distribution of DNMT3B -579 G>T genotypes between the cases and controls. However, in the stratified analysis by clinicopathological characteristic types, we found that statistically, the risk susceptibility to gastric cancer was significantly associated with tumor grade II and GT/TT genotype of patients, compared to patients having GG genotype, (OR = 5.4737, 95% CI = 1.4746. 20.3184, P = 0.01).

conclusionsOur study suggested that the -579 T allele may increase the relative risk for the progression of clinicopathological characteristic of tumor grade of gastric cancer patients.

Indexed as

AdultAgedAged, 80 and overCase-Control StudiesDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BFemaleHumansIranMaleMiddle AgedPolymorphism, GeneticPromoter Regions, GeneticStomach NeoplasmsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BClinicopathological characteristicDNMT3BGastric tumorPolymorphism (579 G>T: rs1569686)

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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.