Evidence map›Paper›PMID 20512145›Full record

ArticleNature genetics2010

A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.

Jin-Xin Bei, Yi Li, Wei-Hua Jia, Bing-Jian Feng, Gangqiao Zhou, Li-Zhen Chen, Qi-Sheng Feng, Hui-Qi Low, Hongxing Zhang, Fuchu He and 5 more

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 227 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
227citing papers in PubMed, 13 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.

NCT01257100 terminatednot on this map

Environmental and Genetic Determinants of NPC

TypeobservationalSponsorNational Cancer Institute (NCI)Ran2010 to 2020Enrolled3,500ConditionsNasopharyngeal Neoplasms, Herpesvirus 4, Human
NCT04094545 completednot on this mapstarted 2018, after this paper: background citation

Intestinal Flora Disruption and a Novel Intestinal Biomarker Associated With Nasopharyngeal Carcinoma

TypeobservationalSponsorThe Third Xiangya Hospital of Central South UniversityRan2018 to 2019Enrolled568ConditionsNasopharyngeal Carcinoma
3 · Its place in the literature

Who cites it

227 citing papers in PubMed, 13 syntheses or guidelines pooled it.

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  6. A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2016
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  11. TNF-α-308G/A polymorphisms and nasopharyngeal cancer risk: a meta-analysis.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2013
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167 more citing papers are in PubMed but not listed here.

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

15 authors.

Jin-Xin BeiState Key Laboratory of Oncology in Southern China, Guangzhou, China.
Yi Li
Wei-Hua Jia
Bing-Jian Feng
Gangqiao Zhou
Li-Zhen Chen
Qi-Sheng Feng
Hui-Qi Low
Hongxing Zhang
Fuchu He
E Shyong Tai
Tiebang Kang
Edison T Liu
Jianjun Liu
Yi-Xin Zeng

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To identify genetic susceptibility loci for nasopharyngeal carcinoma (NPC), a genome-wide association study was performed using 464,328 autosomal SNPs in 1,583 NPC affected individuals (cases) and 1,894 controls of southern Chinese descent. The top 49 SNPs from the genome-wide association study were genotyped in 3,507 cases and 3,063 controls of southern Chinese descent from Guangdong and Guangxi. The seven supportive SNPs were further confirmed by transmission disequilibrium test analysis in 279 trios from Guangdong. We identified three new susceptibility loci, TNFRSF19 on 13q12 (rs9510787, Pcombined=1.53x10(-9), odds ratio (OR)=1.20), MDS1-EVI1 on 3q26 (rs6774494, Pcombined=1.34x10(-8), OR=0.84) and the CDKN2A-CDKN2B gene cluster on 9p21 (rs1412829, Pcombined=4.84x10(-7), OR=0.78). Furthermore, we confirmed the role of HLA by revealing independent associations at rs2860580 (Pcombined=4.88x10(-67), OR=0.58), rs2894207 (Pcombined=3.42x10(-33), OR=0.61) and rs28421666 (Pcombined=2.49x10(-18), OR=0.67). Our findings provide new insights into the pathogenesis of NPC by highlighting the involvement of pathways related to TNFRSF19 and MDS1-EVI1 in addition to HLA molecules.

Indexed as

Polymorphism, Single NucleotideAsian PeopleChinaDNA-Binding ProteinsGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMDS1 and EVI1 Complex Locus ProteinNasopharyngeal NeoplasmsNeoplasm ProteinsOdds RatioProto-OncogenesReceptors, Tumor Necrosis FactorRisk FactorsDNA-Binding ProteinsMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanNeoplasm ProteinsReceptors, Tumor Necrosis FactorTNFRSF19 protein, humanTranscription Factors

Identifiers

PMID20512145

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.