Evidence map›Paper›PMID 25834539›Full record

ArticleAfrican health sciences2015

The association of XRCC3 Thr241Met genetic variant with risk of prostate cancer: a meta-analysis.

Gao Xuan, Ying Hui, He Fang

Open access · diamondAbstract read
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Article in African health sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Association between XRCC3 Thr241Met polymorphism and risk of osteosarcoma in a Chinese population.International journal of clinical and experimental pathology · 2015
    Article
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

3 authors at 1 institution in 1 country.

Gao XuanCollege of Life Science, Anhui Normal University, Wuhu 241000, Hubei Province, People's Republic of China.
Ying HuiCollege of Life Science, Anhui Normal University, Wuhu 241000, Hubei Province, People's Republic of China.
He FangCollege of Life Science, Anhui Normal University, Wuhu 241000, Hubei Province, People's Republic of China.
Anhui Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies suggest that the X-ray repair cross-complementing group 3 gene (XRCC3) Thr241Met genetic variant could be potentially associated with the risk of prostate cancer. However, results from these published studies were conflicting rather than conclusive.

objectiveshis meta-analysis aimed to conduct a better understanding of the effects of XRCC3 Thr241Met genetic variant on prostate cancer risk.

methodsWe identified three eligible studies, 499 prostate cancer cases and 571 controls.

resultsOverall, significant associations were detected in the heterozygote comparison genetic model (CT versus (vs.) CC: OR = 0.71, 95% CI 0.53-0.94, Z =2.38, p= 0.017), and the dominant genetic model (TT/CT vs. CC: OR = 0.74, 95% CI 0.57-0.98, Z = 2.11, p =0.035). In the subgroup analysis by ethnicities, we found that this genetic variant was significantly associated with the decrease risk of prostate cancer in Caucasians for heterozygote comparison genetic model (CT vs. CC: OR = 0.66, 95% CI 0.44-0.98, Z = 2.04, p = 0.042). No publication bias was found in this study.

conclusionsResults from this meta-analysis indicate that the XRCC3 Thr241Met genetic variant is associated with prostate cancer risk.

Indexed as

Genetic Predisposition to DiseaseGenetic VariationCase-Control StudiesDNA-Binding ProteinsHumansMalePolymorphism, GeneticProstatic NeoplasmsRisk FactorsDNA-Binding ProteinsX-ray repair cross complementing protein 3Genetic variantMeta-analysisProstate cancerXRCC3 gene

Identifiers

PMID25834539
PMCPMC4370129
OpenAlexW2042933511

What OpenQuestion holds

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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.