Evidence map›Paper›PMID 26820236›Full record

ArticleJournal of cellular and molecular medicine2016

Association between XPG polymorphisms and stomach cancer susceptibility in a Chinese population.

Yun-Zhi Chen, Fang Guo, Hong-Wei Sun, Hong-Ru Kong, Sheng-Jie Dai, Shi-Hao Huang, Wen-Wei Zhu, Wen-Jun Yang, Meng-Tao Zhou

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 4 pooled it
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 4 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Article
  7. Article
  8. Association ofWorld journal of gastroenterology · 2019
    Article
  9. Article
  10. Bioscience reports · 2018
    Article
  11. Article
  12. Oncotarget · 2017
    Article
  13. Article
  14. Article
  15. Journal of Cancer · 2016
    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

9 authors at 4 institutions in 1 country.

Yun-Zhi ChenDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Fang GuoDepartment of Gynecology and Obstetrics, People's Hospital, Wenzhou, Zhejiang, China.
Hong-Wei SunDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Hong-Ru KongDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Sheng-Jie DaiDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Shi-Hao HuangDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wen-Wei ZhuDepartment of General Surgery, Huashan Hospital, Fudan University Shanghai Cancer Center, Shanghai, China.
Wen-Jun YangDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Meng-Tao ZhouDepartment of General Surgery, First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wenzhou Medical University · CNFirst Affiliated Hospital of Wenzhou Medical University · CNFudan University Shanghai Cancer Center · CNWenzhou City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xeroderma pigmentosum group G (XPG) protein plays an important role in the DNA repair process by cutting the damaged DNA at the 3' terminus. Previous studies have indicated some polymorphisms in the XPG gene are associated with stomach cancer susceptibility. We performed this hospital-based case-control study to evaluate the association of four potentially functional XPG polymorphisms (rs2094258 C>T, rs751402 C>T, rs2296147 T>C and rs873601G>A) with stomach cancer susceptibility. The four single nucleotide polymorphisms (SNPs) were genotyped in 692 stomach cancer cases and 771 healthy controls. Logistic regression analysis was conducted, and odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the association of interest. Of the studied SNPs, XPG rs873601G>A polymorphism was found to significantly associate with stomach cancer susceptibility (AA versus GG/AG: OR = 1.31, 95% CI = 1.03-1.66, P = 0.027). Combined analysis of all SNPs revealed that the individuals with two of risk genotypes had a significantly increased stomach cancer risk (OR = 1.52, 95% CI = 1.13-2.06). In the stratification analysis, the association between the rs873601AA genotype and stomach cancer risk was observed in older group (>59 year), as well as patients with non-cardia stomach cancer. Further combined analysis indicated men, smokers, or non-drinkers more than one risk genotypes had a significantly increased stomach cancer risk. Our results indicate that XPG rs873601G>A polymorphism may be associated with the risk of stomach cancer. Further prospective studies with different ethnicities and large sample sizes are needed to validate our findings.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAgedAllelesAsian PeopleCase-Control StudiesDNA-Binding ProteinsDNA Excision Repair Protein ERCC-5EndonucleasesFemaleGene ExpressionGenotypeHumansLogistic ModelsMaleMiddle AgedDNA-Binding ProteinsDNA Excision Repair Protein ERCC-5EndonucleasesNuclear ProteinsTranscription Factorsgenetic susceptibilitypolymorphismstomach cancerXPG

Identifiers

PMID26820236
PMCPMC4831351
OpenAlexW2256630231

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.