Evidence map›Paper›PMID 23553206›Full record

ArticleInternational journal of cancer2013

Polymorphisms in the XRCC1 gene modify survival of bladder cancer patients treated with chemotherapy.

Carlotta Sacerdote, Simonetta Guarrera, Fulvio Ricceri, Barbara Pardini, Silvia Polidoro, Alessandra Allione, Rossana Critelli, Alessia Russo, Angeline S Andrew, Yuanqing Ye and 12 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
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  6. Review
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  11. Influences of ERCC1, ERCC2, XRCC1, GSTP1, GSTT1, and MTHFR polymorphisms on clinical outcomes in gastric cancer patients treated with EOF chemotherapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  12. Article
  13. Article
  14. XRCC1 polymorphisms associated with survival among Chinese bladder cancer patients receiving epirubicin and mitomycin C.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  15. Article
  16. Immune therapies in non-muscle invasive bladder cancer.Current treatment options in oncology · 2015
    Review
  17. Article
  18. 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

22 authors at 7 institutions in 4 countries.

Carlotta SacerdoteHuGeF Human Genetics Foundation, Torino, Italy. carlotta.sacerdote@cpo.it
Simonetta Guarrera
Fulvio Ricceri
Barbara Pardini
Silvia Polidoro
Alessandra Allione
Rossana Critelli
Alessia Russo
Angeline S Andrew
Yuanqing Ye
Xifeng Wu
Lambertus A Kiemeney
Andrea Bosio
Giovanni Casetta
Giuseppina Cucchiarale
Paolo Destefanis
Paolo Gontero
Luigi Rolle
Andrea Zitella
Dario Fontana
Paolo Vineis
Giuseppe Matullo
Italian institute for Genomic Medicine · ITAzienda Ospedaliero Universitaria San Giovanni Battista · ITUniversity of Turin · ITThe University of Texas MD Anderson Cancer Center · USDartmouth College · USRadboud University Medical Center · NLRadboud University Nijmegen · NL

Funding

Targeting Ral GTPases in Bladder CancerP50CA091846 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DINNEY, COLIN P.N., MCCONKEY, DAVID J. · 2001 to 2018
$37.4M
Quantitative Biology Research InstituteP20GM103534 · NIGMS · DARTMOUTH COLLEGE · PI AMOS, CHRISTOPHER I. · 2012 to 2016
$8.6M
QUANTITATIVE BIOLOGY RESEARCH INSTITUTEP20RR024475 · NCRR · DARTMOUTH COLLEGE · PI MOORE, JASON H. · 2011 to 2011
$2.3M
Bladder Cancer Prognostic IndicatorsK07CA102327 · NCI · DARTMOUTH COLLEGE · PI ANDREW, ANGELINE SANDERSON · 2005 to 2009
$819k
NCI NIH HHS K07 CA102327NCI NIH HHS P50 CA091846NCRR NIH HHS P20 RR024475NIGMS NIH HHS P20 GM103534
6 · The paper itself

Abstract

Survival of bladder cancer patients depends on several factors including disease stage and grade at diagnosis, age, health status of the patient and the applied treatment. Several studies investigated the role of DNA repair genetic variants in cancer susceptibility, but only few studies investigated their role in survival and response to chemotherapy for bladder cancer. We genotyped 28 single nucleotide polymorphisms (SNP) in DNA repair genes in 456 bladder cancer patients, reconstructed haplotypes and calculated a score for combinations of the SNPs. We estimated Hazard Ratios (adjHR) for time to death. Among patients treated with chemotherapy, variant alleles of five SNPs in the XRCC1 gene conferred better survival (rs915927 adjHR 0.55 (95%CI 0.32-0.94); rs76507 adjHR 0.48 (95%CI 0.27-0.84); rs2854501 adjHR 0.25 (95%CI 0.12-0.52); rs2854509 adjHR 0.21 (95%CI 0.09-0.46); rs3213255 adjHR 0.46 (95%CI 0.26-0.80). In this group of patients, an increasing number of variant alleles in a XRCC1 gene score were associated with a better survival (26% decrease of risk of death for each additional variant allele in XRCC1). By functional analyses we demonstrated that the previous XRCC1 SNPs confer lower DNA repair capacity. This may support the hypothesis that survival in these patients may be modulated by the different DNA repair capacity determined by genetic variants. Chemotherapy treated cancer patients bearing an increasing number of "risky" alleles in XRCC1 gene had a better survival, suggesting that a proficient DNA repair may result in resistance to therapy and shorter survival. This finding may have clinical implications for the choice of therapy.

Indexed as

AdultAgedAllelesDNA-Binding ProteinsDNA RepairGenetic Predisposition to DiseaseGenetic VariationGenotypeHumansMaleMiddle AgedPolymorphism, Single NucleotidePrognosisSurvivalUrinary Bladder NeoplasmsX-ray Repair Cross Complementing Protein 1DNA-Binding ProteinsX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanbladder cancerchemotherapyDNA repair genessurvivalXRCC1

Identifiers

PMID23553206
PMCPMC3804126
OpenAlexW2161308107

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.