Evidence map›Paper›PMID 32192442›Full record

ArticleBMC cancer2020

MTHFR, XRCC1 and OGG1 genetic polymorphisms in breast cancer: a case-control study in a population from North Sardinia.

Matteo Floris, Daria Sanna, Paolo Castiglia, Carlo Putzu, Valeria Sanna, Antonio Pazzola, Maria Rosaria De Miglio, Francesca Sanges, Giovanna Pira, Antonio Azara and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

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  9. Associations of theBiomedical reports · 2021
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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

17 authors at 3 institutions in 1 country.

Matteo FlorisDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy. mfloris@uniss.it.
Daria SannaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Paolo CastigliaDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
Carlo PutzuDivision of Medical Oncology, AOU Sassari, Sassari, Italy.
Valeria SannaDivision of Medical Oncology, AOU Sassari, Sassari, Italy.
Antonio PazzolaDivision of Medical Oncology, AOU Sassari, Sassari, Italy.
Maria Rosaria De MiglioDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
Francesca SangesDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Giovanna PiraDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Antonio AzaraDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
Emanuele LampisDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
Antonello SerraUnit of Occupational Medicine, AOU Sassari, Sassari, Italy.
Ciriaco CarruDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Maristella SteriInstitute for Genetic and Biomedical Research, National Research Council (CNR), Monserrato, Cagliari, Italy.
Flavia CostanzaDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Marco BisailLILT, Sassari, Italy.
Maria Rosaria MuroniDepartment of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy. mrmuroni@uniss.it.
University of Sassari · ITAzienda Ospedaliero Universitaria di Sassari · ITNational Research Council · IT

Funding

Fondazione di Sardegna, Bando "Salute Pubblica, Medicina Preventiva e Riabilitativa", Anno 2018. U408.2019/AI.373.PL
6 · The paper itself

Abstract

backgroundDespite conflicting results, considerable evidence suggests the association between single nucleotide polymorphisms in MTHFR, XRCC1 and OGG1 genes and, risk of developing breast cancer. Here a case-control study is reported, including 135 breat cancer patients and 112 healthy women, all representative of Northern Sardinian population.

methodsPolymerase chain reaction/restriction fragment length polymorphism method was used to determine the genotypes of five polymorphisms: MTHFR C677T (rs1801133) and A1298C (rs1801131), XRCC1 Arg194Trp (rs1799782) and Arg399Gln (rs25487) and OGG1 Ser326Cys (rs1052133). Allelic, genotypic and haplotype association analyses with disease risk and clinicopathological parameters were performed.

resultsA nominally significant association with breast cancer risk was observed for MTHFR C677T polymorphism heterozygous genotype in the codominant model (OR: 0.57, 95% CI: 0.32-1.00, p = 0.049) and for Cys/Cys genotype of the OGG1 Ser326Cys polymorphism in the recessive model (OR: 0.23, 95% CI: 0.05-1.11, p = 0.0465). No significant differences were found at genotype-level for A1298C polymorphism of the MTHFR gene and Arg194Trp and Arg399Gln of the XRCC1 gene. Furthermore, the OGG1 and XRCC1 rs25487 polymorphisms were nominally associated with PgR, Her2 status and with sporadic breast cancer, respectively.

conclusionsBased on genetic characteristics of individuals included in this study, results suggest that MTHFR CT and OGG1 Cys/Cys genotypes have a protective effect that may have an influence on breast cancer risk in a representative Northern Sardinian population.

Indexed as

Polymorphism, Single NucleotideBreast NeoplasmsCase-Control StudiesDNA GlycosylasesFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotyping TechniquesHaplotypesHumansItalyMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedX-ray Repair Cross Complementing Protein 1DNA GlycosylasesMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanoxoguanine glycosylase 1, humanX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanMediterranean populationMTHFR SNPsOGG1 SNPsXRCC1 SNPs

Identifiers

PMID32192442
PMCPMC7083022
OpenAlexW3010744970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.