Evidence map›Paper›PMID 25921222›Full record

ArticleInternational journal of epidemiology2015

Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers.

Hyuna Sung, Howard H Yang, Han Zhang, Qi Yang, Nan Hu, Ze-Zhong Tang, Hua Su, Lemin Wang, Chaoyu Wang, Ti Ding and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in International journal of epidemiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

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  13. Cancer subtypes in aetiological research.European journal of epidemiology · 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

25 authors at 8 institutions in 2 countries.

Hyuna SungDivision of Cancer Epidemiology and Genetics, and.
Howard H YangLaboratory of Population Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Han ZhangDivision of Cancer Epidemiology and Genetics, and.
Qi YangDivision of Cancer Epidemiology and Genetics, and.
Nan HuDivision of Cancer Epidemiology and Genetics, and.
Ze-Zhong TangShanxi Cancer Hospital, Taiyuan, People's Republic of China.
Hua SuDivision of Cancer Epidemiology and Genetics, and.
Lemin WangDivision of Cancer Epidemiology and Genetics, and.
Chaoyu WangDivision of Cancer Epidemiology and Genetics, and.
Ti DingShanxi Cancer Hospital, Taiyuan, People's Republic of China.
Jin-Hu FanDepartment of Epidemiology, Cancer Institute (Hospital), Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
You-Lin QiaoDepartment of Epidemiology, Cancer Institute (Hospital), Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
William WheelerInformation Management Services, Silver Spring, MD, USA and.
Carol GiffenInformation Management Services, Silver Spring, MD, USA and.
Laurie BurdettCancer Genomics Research Laboratory, NCI-Frederick, SAIC-Frederick Inc., Frederick, MD, USA.
Zhaoming WangDivision of Cancer Epidemiology and Genetics, and Cancer Genomics Research Laboratory, NCI-Frederick, SAIC-Frederick Inc., Frederick, MD, USA.
Maxwell P LeeLaboratory of Population Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Stephen J ChanockDivision of Cancer Epidemiology and Genetics, and.
Sanford M DawseyDivision of Cancer Epidemiology and Genetics, and.
Neal D FreedmanDivision of Cancer Epidemiology and Genetics, and.
Christian C AbnetDivision of Cancer Epidemiology and Genetics, and.
Alisa M GoldsteinDivision of Cancer Epidemiology and Genetics, and.
Kai YuDivision of Cancer Epidemiology and Genetics, and.
Philip R TaylorDivision of Cancer Epidemiology and Genetics, and.
Paula L HylandDivision of Cancer Epidemiology and Genetics, and hylandpl@mail.nih.gov.
Division of Cancer Epidemiology and GeneticsCancer Genetics (United States) · USChinese Academy of Medical Sciences & Peking Union Medical College · CNInformation Management Services · USShanxi Provincial Cancer Hospital · CNNational Cancer Institute · USNational Institutes of Health · USScience Applications International Corporation (United States) · US

Funding

Intramural NIH HHS
6 · The paper itself

Abstract

backgroundPopulations in north central China are at high risk for oesophageal squamous cell carcinoma (ESCC) and gastric cancer (GC), and genetic variation in epigenetic machinery genes and pathways may contribute to this risk.

methodsWe used the adaptive multilocus joint test to analyse 192 epigenetic genes involved in chromatin remodelling, DNA methylation and microRNA biosynthesis in 1942 ESCC and 1758 GC cases [1126 cardia (GCA) and 632 non-cardia adenocarcinoma (GNCA)] and 2111 controls with Chinese ancestry. We examined potential function of risk alleles using in silico and expression quantitative trait loci (eQTLs) analyses.

resultsSuggestive pathway-based associations were observed for the overall epigenetic (P-value(PATH) = 0.034) and chromatin remodelling (P-value(PATH) = 0.039) pathways with risk of GCA, but not GC, GNCA or ESCC. Overall, 37 different epigenetic machinery genes were associated with risk of one or more upper gastrointestinal (UGI) cancer sites (P-value(GENE )< 0.05), including 14 chromatin remodelling genes whose products are involved in the regulation of HOX genes. We identified a gastric eQTL (rs12724079; rho = 0.37; P = 0.0006) which regulates mRNA expression of ASH1L. Several suggestive eQTLs were also found in oesophageal (rs10898459 in EED), gastric cardia (rs7157322 in DICER1; rs8179271 in ASH1L), and gastric non-cardia (rs1790733 in PPP1CA) tissues.

conclusionsResults of our analyses provide limited but suggestive evidence for a role of epigenetic gene variation in the aetiology of UGI cancer.

Indexed as

DNA MethylationEpigenesis, GeneticAdenocarcinomaAgedAsian PeopleCarcinoma, Squamous CellCase-Control StudiesChinaEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGenetic Predisposition to DiseaseHumansLogistic ModelsMaleMiddle Agedchromatin remodellingDNA methylationEpigeneticsgastric cancergastric cardiagastric non-cardiagene-basedmicroRNAoesophageal squamous cell carcinomapathway-basedSNP

Identifiers

PMID25921222
PMCPMC4598798
OpenAlexW2048482227

What OpenQuestion holds

Textmetadata
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.