Evidence map›Paper›PMID 32936247›Full record

Observational studyBioscience reports2020

Prediction of gastric cancer risk: association between ZBTB20 genetic variance and gastric cancer risk in Chinese Han population.

Fei Bai, Ke Xiao

Abstract readObservational Study
In one paragraph

Observational study in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Contribution ofPharmacogenomics and personalized medicine · 2022
    Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Fei BaiDepartment of Gastroduodenal Pancreas Surgery, Hunan Cancer Hospital, Changsha, 410013, Hunan, P.R. China.
Ke XiaoDepartment of Gastroduodenal Pancreas Surgery, Hunan Cancer Hospital, Changsha, 410013, Hunan, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) is a complex multifactorial disease. Previous studies have revealed genetic variations associated with the risk of gastric cancer. The purpose of the present study was to determine the correlation between single-nucleotide polymorphisms (SNPs) of ZBTB20 and the risk of gastric cancer in Chinese Han population.

methodsWe conducted a 'case-control' study involving 509 GC patients and 507 healthy individuals. We selected four SNPs of ZBTB20 (10934270 T/C, rs9288999 G/A, rs9841504 G/C and rs73230612 C/T), and used logistic regression to analyze the relationship between those SNPs and GC risk under different genetic models; multi-factor dimensionality reduction (MDR) was used to analyze the interaction of "SNP-SNP" in gastric cancer risk; ANOVA and univariate analysis were used to analyze the differences in clinical characteristics among different genotypes.

resultsOur results showed that ZBTB20 rs9288999 is a protective factor for the risk of gastric cancer in multiple genetic models, of which the homozygous model is the most significant (OR = 0.48, P=0.0003); we also found that rs9288999 showed a significant correlation with reducing the risk of gastric cancer in different subgroups (BMI; age; gender; smoking or drinking status; adenocarcinoma); rs9841504 is associated with increased GC risk in the participants with BMI>24 kg/m2; rs9841504 and rs73230612 are certainly associated with clinical characteristics of platelet and carbohydrate antigen 242, respectively.

conclusionOur results suggest that ZBTB20 rs9288999 may be important for reducing the risk of GC in the Chinese Han population.

Indexed as

AdenocarcinomaAgedAlcohol DrinkingAsian PeopleBody Mass IndexCase-Control StudiesChinaFemaleHumansMaleMiddle AgedModels, GeneticNerve Tissue ProteinsPolymorphism, Single NucleotideProtective FactorsRisk AssessmentNerve Tissue ProteinsTranscription FactorsZBTB20 protein, humanCase-control studygastric cancersingle nucleotide polymorphismsZBTB20

Identifiers

PMID32936247
PMCPMC7517264

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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.