Evidence map›Paper›PMID 27669275›Full record

ArticleInternational journal of environmental research and public health2016

Polymorphisms in GEMIN4 and AGO1 Genes Are Associated with the Risk of Lung Cancer: A Case-Control Study in Chinese Female Non-Smokers.

Xue Fang, Zhihua Yin, Xuelian Li, Lingzi Xia, Baosen Zhou

Open access · goldAbstract readComparative Study
In one paragraph

Article in International journal of environmental research and public health, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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  17. Association ofOncoTargets and therapy · 2017
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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

5 authors at 1 institution in 1 country.

Xue FangDepartment of Epidemiology, School of Public Health, China Medical University, Shenyang 110122, China. fangxue222@hotmail.com.
Zhihua YinDepartment of Epidemiology, School of Public Health, China Medical University, Shenyang 110122, China. zhyin@mail.cmu.edu.cn.
Xuelian LiDepartment of Epidemiology, School of Public Health, China Medical University, Shenyang 110122, China. xlli@mail.cmu.edu.cn.
Lingzi XiaDepartment of Epidemiology, School of Public Health, China Medical University, Shenyang 110122, China. xialingzi1013@hotmail.com.
Baosen ZhouDepartment of Epidemiology, School of Public Health, China Medical University, Shenyang 110122, China. bszhou@mail.cmu.edu.cn.
Liaoning University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA biosynthesis genes can affect the regulatory effect of global microRNAs to target mRNA and hence influence the genesis and development of human cancer. Here, we selected five single nucleotide polymorphisms (SNPs) (rs7813, rs2740349, rs2291778, rs910924, rs595961) in two key microRNA biosynthesis genes (GEMIN4 and AGO1) and systematically evaluated the association between these SNPs, the gene-environment interaction and lung cancer risk. To control the impact of cigarette smoking on lung cancer, we recruited Chinese female non-smokers for the study. The total number of lung cancer cases and cancer-free controls were 473 and 395 in the case-control study. Four SNPs showed statistically significant associations with lung cancer risk. After Bonferroni correction, rs7813 and rs595961 were evidently still associated with lung cancer risk. In the stratified analysis, our results revealed that all five SNPs were associated with the risk of lung adenocarcinoma; after Bonferroni correction, significant association was maintained for rs7813, rs910924 and rs595961. Haplotype analysis showed GEMIN4 haplotype C-A-G-T was a protective haplotype for lung cancer. In the combined unfavorable genotype analysis, with the increasing number of unfavorable genotypes, a progressively increased gene-dose effect was observed in lung adenocarcinoma. We also found that individuals exposed to cooking oil fumes showed a relatively high risk of lung cancer, but no interactions were found between cooking oil fume exposure or passive smoking exposure with these SNPs, either on an additive scale or a multiplicative scale. Overall, this is the first study showing that rs7813 and rs595961 could be meaningful as genetic markers for lung cancer risk.

Indexed as

Gene-Environment InteractionAdenocarcinomaAdenocarcinoma of LungAgedAsian PeopleCase-Control StudiesCookingFemaleGenotypeHaplotypesHumansLung NeoplasmsMicroRNAsMiddle AgedPolymorphism, Single NucleotideRiskMicroRNAsAGO1cooking oil fumesGEMIN4lung cancerpassive smokingsingle nucleotide polymorphismsusceptibility

Identifiers

PMID27669275
PMCPMC5086678
OpenAlexW2521332829

What OpenQuestion holds

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LicenceCC BY
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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.