Evidence map›Paper›PMID 32711433›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2020

Association of DNA Repair Genes XRCC1 and APE-1 with the Risk of Cervical Cancer in North Indian population.

Mark Rector Charles, Syed Tasleem Raza, Rolee Sharma, Pushpendra Pratap, Ale Eba, Manvendra Singh

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Molecular Features of HPV-Independent Cervical Cancers.Pathogens (Basel, Switzerland) · 2025
    Review
  2. 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

6 authors at 1 institution in 1 country.

Mark Rector CharlesDepartment of Biotechnology, Era's Lucknow Medical College and Hospital, Lucknow, India.
Syed Tasleem RazaDepartment of Biotechnology, Era's Lucknow Medical College and Hospital, Lucknow, India.
Rolee SharmaDepartment of Bioscience, Integral University Lucknow, Lucknow Uttar Pradesh, India.
Pushpendra PratapDepartment of Biotechnology, Era's Lucknow Medical College and Hospital, Lucknow, India.
Ale EbaDepartment of Biotechnology, Era's Lucknow Medical College and Hospital, Lucknow, India.
Manvendra SinghCentre of Bio-Medical Research (CMBRL), Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Era's Lucknow Medical College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundsCervical cancer (CC) is one of the leading cause of death in women worldwide, HPV infection is the major risk factor in the disease development, 0and however other risk factor such as chemical carcinogens, genetic susceptibility and altered immune system are also a cause of the disease progression. In the light of the above statement we studied the base excision repair pathway (BER).

methodsWe identified and studied the association of Single Nucleotide polymorphisms in the DNA repair genes of XRCC1 (Arg194Trp, Arg399G,) and APE-1Asp/148Glu to the susceptibility of cervical cancer (CC) in North Indian population. In our study of cases (n=102). Controls (n=109) were recruited from among women without cervical abnormalities. Genotypes were determined by PCR-CTPP method, Taking DNA from peripheral blood in a case control study.

resultsA positive association was observed between the polymorphisms of XRCC1 genes, that is, in codons 194 (P=0.03, odds ratio (OR) =2.39, 95% confidence interval (CI)=5.2-1.1), 280 (P=0.01, OR=4.1, 95% CI=11.5-1.3) and 399 (P=0.01, OR=3.4, 95% CI=8.6-1.3) while APE-1 genotype GG (p=0.03,odds ratio(OR)=0.2,95% confidence interval (CI)=0.97-0.004) we observed a statistically significant protective role in developing cervical cancer.

conclusionOur results suggested that, XRCC1 gene is an important candidate gene for susceptibility to cervical cancer. Although the sample size was small, the present study indicate a statistical association between cervical cancer and XRCC1 SNPs. Future studies are needed that may provide a better understanding of the association between gene polymorphism and cervical carcinoma risk.<br />.

Indexed as

DNA RepairAdenocarcinomaBiomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesDNA-(Apurinic or Apyrimidinic Site) LyaseFemaleFollow-Up StudiesGenetic Predisposition to DiseaseHumansMiddle AgedPolymorphism, Single NucleotidePrognosisUterine Cervical NeoplasmsX-ray Repair Cross Complementing Protein 1APEX1 protein, humanBiomarkers, TumorDNA-(Apurinic or Apyrimidinic Site) LyaseX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanAPE-1Base excision repairCervical cancergene polymorphismXRCC1

Identifiers

PMID32711433
PMCPMC7573399
OpenAlexW3044152238

What OpenQuestion holds

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LicenceCC BY
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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.