Evidence map›Paper›PMID 40963005›Full record

SynthesisAmino acids2025

Associations between XRCC1-Arg399Gln polymorphism and the risk of prostate cancer: an updated meta-analysis.

Jiang Deng, Lihua Xu, Jun Zhou, He Huang

Abstract readMeta-Analysis
In one paragraph

Synthesis in Amino acids, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. Genetic Polymorphisms and Antioxidant Reactions in Prostate Cancer.International journal of molecular sciences · 2026
    Review
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

4 authors.

Jiang Deng *Hubei No. 3 People's Hospital of Jianghan University, Wuhan, China. 15972096274@163.com.
Lihua Xu *Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, 430016, Hubei, People's Republic of China.
Jun ZhouHubei No. 3 People's Hospital of Jianghan University, Wuhan, China.
He HuangHubei No. 3 People's Hospital of Jianghan University, Wuhan, China. water201405@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The X-ray repair cross-complementary group 1 (XRCC1) gene 399 codon polymorphism may alter the structure of DNA repair enzymes to regulate DNA repair capacity. Impaired DNA repair ability can lead to the development of cancers such as prostate cancer (PCa). Although the association between the XRCC1 codon 399 polymorphism and the risk of PCa has been widely reported, the results have not been clear. Data were collected from PubMed, EMBASE, the Wanfang Database, CNKI and the Web of Science. A total of 20 case‒control studies were selected for inclusion in this updated analysis to determine the association between the XRCC1 codon 399 polymorphism and the risk of PCa. The crude odds ratio (OR) and 95% confidence interval (CI) were calculated using Stata (version 18) software to evaluate the association between the XRCC1-Arg399Gln polymorphism and prostate cancer. We identified 20 eligible reports that included 5803 cases of prostate cancer and 5470 controls. Our meta-analysis revealed a significant association between the XRCC1-Arg399Gln polymorphism and the risk of prostate cancer. In particular, according to the recessive models, this polymorphism was associated with a significantly increased prevalence of prostate cancer in Asian populations (AA versus AG + GG: OR = 1.255, 95% CI = 1.063-1.481, P = 0.507, I

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticPolymorphism, Single NucleotideProstatic NeoplasmsX-ray Repair Cross Complementing Protein 1Asian PeopleCase-Control StudiesHumansMaleRisk FactorsX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanPolymorphismProstate cancer (PCa)XRCC1-Arg399Gln

Identifiers

PMID40963005
PMCPMC12443860

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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.