Evidence map›Paper›PMID 26668074›Full record

ArticleScientific reports2015

Variants and haplotypes in Flap endonuclease 1 and risk of gallbladder cancer and gallstones: a population-based study in China.

Xingyuan Jiao, Ying Wu, Liansuo Zhou, Jinyun He, Chonghua Yang, Peng Zhang, Ronglin Hu, Canqiao Luo, Jun Du, Jian Fu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Xingyuan JiaoDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Ying WuDepartment of Biostatistics, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Liansuo ZhouDepartment of General Surgery, The First Affiliated Hospital, Xian Medical College, Xian 710061, China.
Jinyun HeDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Chonghua YangDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Peng ZhangDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Ronglin HuDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Canqiao LuoDeparment of Pathology, Sun Yat-Sen University School of Medicine, Guangzhou 510080, China.
Jun DuDepartment of Molecular Biology, Sun Yat-Sen University School of Pharmacy, Guangzhou 510080, China.
Jian FuDepartment of General Surgery and Transplantation Surgery, University Hospital Duisburg-Essen, D-45122, Germany.
Jinsen ShiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital, Xian Jiaotong University, Xian 710061, China.
Rui HeDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Dongming LiDepartment of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Wang JunDepartment of Anatomy, Shenzhen University School of Medicine, Shenzhen 518060, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNUniversity of Duisburg-Essen · DEFirst Affiliated Hospital of Xi'an Jiaotong University · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of FEN1 genetic variants on gallstone and gallbladder cancer susceptibility is unknown. FEN1 SNPs were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method in blood samples from 341 gallbladder cancer patients and 339 healthy controls. The distribution of FEN1-69G > A genotypes among controls (AA, 20.6%; GA, 47.2% and GG 32.2%) was significantly different from that among gallbladder cancer cases (AA, 11.1%; GA, 48.1% and GG, 40.8%), significantly increased association with gallbladder cancer was observed for subjects with both the FEN1-69G > A GA (OR = 1.73, 95% CI = 1.01-2.63) and the FEN1-69G > A GG (OR = 2.29, 95% CI = 1.31-3.9). The distribution of FEN1 -4150T genotypes among controls (TT, 21.8%;GT, 49.3% and GG 28.9%) was significantly different from that among gallbladder cancer cases (TT, 12.9%; GT, 48.4% and GG 38.7%), significantly increased association with gallbladder cancer was observed for subjects with both the FEN1-4150T GT(OR = 1.93, 95% CI = 1.04-2.91) and the FEN1-4150T GG(OR = 2.56, 95% CI = 1.37-5.39). A significant trend towards increased association with gallbladder cancer was observed with potentially higher-risk FEN1-69G > A genotypes (P < 0.001, χ2 trend test) and FEN14150G > T (P < 0.001, χ2 trend test) in gallstone presence but not in gallstone absence (P = 0.81, P = 0.89, respectively). In conclusion, this study revealed firstly that FEN1 polymorphisms and haplotypes are associated with gallbladder cancer risk.

Indexed as

HaplotypesPolymorphism, Single NucleotideAgedAged, 80 and overAsian PeopleChinaFemaleFlap EndonucleasesGallbladder NeoplasmsGallstonesGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansLinkage DisequilibriumMaleFlap Endonucleases

Identifiers

PMID26668074
PMCPMC4678911
OpenAlexW2201597344

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.