Evidence map›Paper›PMID 24956286›Full record

ArticleGenetic testing and molecular biomarkers2014

Haplotype analysis of the XRCC1 gene and laryngeal cancer.

Wei Chen, Li Xu, Zhi-Yi Wang, Li-Jun Xue, Feng-Lei Xue, Man-Jie Jiang, Qiu-Ping Wang, Hong-Liang Zheng

Open access · greenAbstract read
In one paragraph

Article in Genetic testing and molecular biomarkers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 35% 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

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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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 3 institutions in 1 country.

Wei Chen1 Department of Otolaryngology-Head and Neck Surgery, Jinling Hospital, Nanjing Clinical Medical College, Second Military Medical University , Nanjing, Jiangsu, People's Republic of China .
Li Xu
Zhi-Yi Wang
Li-Jun Xue
Feng-Lei Xue
Man-Jie Jiang
Qiu-Ping Wang
Hong-Liang Zheng
Second Affiliated Hospital of Nanjing Medical University · CNJinling Institute of Technology · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSeveral polymorphisms in DNA repair genes have been extensively studied in association with various human cancers, including laryngeal cancer. The present study aimed to investigate the association between polymorphisms of the XRCC1 gene and laryngeal cancer in a Chinese population.

methodsFive polymorphisms of the XRCC1 gene (rs3213403, rs1799778, rs1001581, rs3213282, and rs3810378) were genotyped by TaqMan in 234 patients with larynx cancer and 230 age- and sex-matched controls without cancer.

resultsThe rs3213403, rs1799778, and rs3213282 polymorphisms of XRCC1 were associated with larynx cancer. Haplotype analysis indicated that CCA (odds ratio [OR], 5.707; 95% confidence interval [CI], 3.277-9.938; p<0.001), TGG (OR, 4.344; 95% CI, 2.804-6.732; p<0.001), ACA (OR, 1.615; 95% CI, 1.159-2.250; p=0.004), and GCG (OR, 1.702; 95% CI, 1.164-2.489; p=0.005) were associated with an increased risk for larynx cancer, respectively. However, TGA (OR, 0.518; 95% CI, 0.398-0.673; p<0.001) and ACC (OR, 0.314; 95% CI, 0.215-0.457; p<0.001) were associated with a decreased risk for larynx cancer.

conclusionsThe results indicated that XRCC1 genetic polymorphisms were associated with larynx cancer in a Chinese population.

Indexed as

HaplotypesAdultAgedAged, 80 and overBiomarkers, TumorCase-Control StudiesChinaDNA-Binding ProteinsFemaleHumansLaryngeal NeoplasmsMaleMiddle AgedReverse Transcriptase Polymerase Chain ReactionX-ray Repair Cross Complementing Protein 1Biomarkers, TumorDNA-Binding ProteinsX-ray Repair Cross Complementing Protein 1XRCC1 protein, human

Identifiers

PMID24956286
PMCPMC4094024
OpenAlexW2409768773

What OpenQuestion holds

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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.