Evidence map›Paper›PMID 26617897›Full record

ArticleInternational journal of clinical and experimental pathology2015

Polymorphism within the distal RAD51 gene promoter is associated with colorectal cancer in a Polish population.

Bartosz Mucha, Jacek Kabzinski, Adam Dziki, Karolina Przybylowska-Sygut, Andrzej Sygut, Ireneusz Majsterek, Lukasz Dziki

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Journal of oncology · 2019
    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

7 authors at 2 institutions in 1 country.

Bartosz MuchaDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz Poland.
Jacek KabzinskiDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz Poland.
Adam DzikiDepartment of General and Colorectal Surgery Medical University in Lodz Poland.
Karolina Przybylowska-SygutDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz Poland.
Andrzej SygutDepartment of General and Vascular Surgery, Medical Center of Pabianice Poland.
Ireneusz MajsterekDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz Poland.
Lukasz DzikiDepartment of General and Colorectal Surgery Medical University in Lodz Poland.
Medical University of Lodz · PLMedical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is one of the most common cancers in developed countries. Annually, over one million of new cases in the world are recorded. Majority of CRCs occur sporadically with dominant phenotype of chromosomal instability (CIN). Permanent exposure to DNA damaging agents such as ionizing radiation result in DNA double-stranded breaks, which create favorable conditions for chromosomal aberration to arise. Homologous recombination repair (HRR) is the leading process engaged in maintaining of the genome integrity. RAD51 protein was recognized as crucial in HRR. Single nucleotide polymorphisms are the primary source of genetic variation which presence in the RAD51 promoter region can affect on its expression and consequently modulate HR efficiency.

objectivesThe aim of this study was to analyze the distribution of genotypes and allele frequencies of -4791A/T and -4601A/G RAD51 gene polymorphisms, followed by an assessment of their relationship with the risk of CRC. MATERIAL AND

methodsThe study included 115 patients with confirmed CRC. Control group was consisted of 118 cancer-free individuals with a negative family history. The genotypes were identified by PCR-RFLP method.

conclusionThis study revealed statistically significant association between appearance of G/A genotype in position -4601 of RAD51 gene and CRC risk.

Indexed as

AgedCase-Control StudiesColorectal NeoplasmsDNA RepairFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHomologous RecombinationHumansMaleMiddle AgedPhenotypePolandPolymorphism, Single NucleotidePromoter Regions, GeneticRAD51 protein, humanRad51 Recombinasecolorectal cancerDNA double strand breaksHomologous recombination repairsingle nucleotide polymorphism

Identifiers

PMID26617897
PMCPMC4637713
OpenAlexW2412953952

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.