Evidence map›Paper›PMID 22927776›Full record

ArticleInternational journal of medical sciences2012

Interaction between polymorphisms of DNA repair genes significantly modulated bladder cancer risk.

Yi Zhi, Jing Yu, Yang Liu, Quanfang Wei, Fang Yuan, Xiaozhou Zhou, Bo Song, Zhiwen Chen, Jin Yang

Abstract read
In one paragraph

Article in International journal of medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 7 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.

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

18 citing papers in PubMed, 7 syntheses or guidelines pooled it.

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  3. XPC gene polymorphisms contribute to bladder cancer susceptibility: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
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  4. XRCC1 polymorphisms increase bladder cancer risk in Asians: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
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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

9 authors.

Yi ZhiDepartment of Cell Biology, Third Military Medical University, Chongqing, China.
Jing Yu
Yang Liu
Quanfang Wei
Fang Yuan
Xiaozhou Zhou
Bo Song
Zhiwen Chen
Jin Yang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA repair is a primary defense mechanism against damage caused by exogenous and endogenous sources. We examined the associations between bladder cancer and 7 polymorphisms from 5 genes involved in the maintenance of genetic stability (MMR: MLH1-93G>A; BER: XRCC1--77T>C and Arg399Gln; NER:XPC Lys939Gln and PAT +/-; DSBR:ATM G5557A and XRCC7 G6721T) in 302 incident bladder cancer cases and 311 hospital controls. Genotyping was done using a polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) technique. The homozygous variant of XRCC7 G6721T (Odds Ratio [OR]: 2.36; 95% Confidence Interval [CI]: 1.13-4.92) was associated with increased bladder cancer risk. In an analysis of combined genotypes, the combination of XRCC1Arg399Gln (Gln allele) with XRCC1-77 T/T led to an increase in risk (OR: 1.61; 95% CI: 1.10-2.36). Moreover, when the XPCLys939Gln (Gln allele) (nucleotide excision repair [NER]) was present together with XRCC7 (T allele) (double strand break repair [DSBR]), the bladder cancer risk dramatically increased (OR: 4.42; 95% CI: 1.23-15.87). Our results suggest that there are multigenic variations in the DNA repair pathway involved in bladder cancer susceptibility, despite the existence of ethnic group differences.

Indexed as

Adaptor Proteins, Signal TransducingAdultDNA-Activated Protein KinaseDNA-Binding ProteinsDNA RepairFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedMutL Protein Homolog 1Nuclear ProteinsPolymorphism, GeneticUrinary Bladder NeoplasmsX-ray Repair Cross Complementing Protein 1Young AdultAdaptor Proteins, Signal TransducingDNA-Activated Protein KinaseDNA-Binding ProteinsMLH1 protein, humanMutL Protein Homolog 1Nuclear ProteinsPRKDC protein, humanXPC protein, humanX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanAtaxia telangiectasia mutatedDNA repairMultigenic variations.MutL homolog 1PolymorphismTransitional cell carcinoma

Identifiers

PMID22927776
PMCPMC3427955

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.