Evidence map›Paper›PMID 29332455›Full record

ArticleTechnology in cancer research & treatment2017

DNA Repair Mechanism Gene, XRCC1A ( Arg194Trp) but not XRCC3 ( Thr241Met) Polymorphism Increased the Risk of Breast Cancer in Premenopausal Females: A Case-Control Study in Northeastern Region of India.

K Rekha Devi, Jishan Ahmed, Kanwar Narain, Kaustab Mukherjee, Gautam Majumdar, Saia Chenkual, Jason C Zonunmawia

Open access · greenAbstract read
In one paragraph

Article in Technology in cancer research & treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Genetic variants of thePrzeglad menopauzalny = Menopause review · 2024
    Article
  3. Article
  4. Article
  5. Association ofClinical and experimental gastroenterology · 2020
    Article
  6. 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 4 institutions in 1 country.

K Rekha Devi1 Regional Medical Research Centre, NE Region, Indian Council of Medical Research, Dibrugarh, Assam, India.
Jishan Ahmed2 Assam Medical College and Hospital, Dibrugarh, Assam, India.
Kanwar Narain1 Regional Medical Research Centre, NE Region, Indian Council of Medical Research, Dibrugarh, Assam, India.
Kaustab Mukherjee1 Regional Medical Research Centre, NE Region, Indian Council of Medical Research, Dibrugarh, Assam, India.
Gautam Majumdar3 Regional Cancer Centre, Agartala, Tripura, India.
Saia Chenkual4 Civil Hospital, Aizawl, Mizoram, India.
Jason C Zonunmawia4 Civil Hospital, Aizawl, Mizoram, India.
Aizawl Adventist Hospital · INIndian Council of Medical Research · INRegional Medical Research Centre · INAssam Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-ray repair cross complementary group gene is one of the most studied candidate gene involved in different types of cancers. Studies have shown that X-ray repair cross complementary genes are significantly associated with increased risk of breast cancer in females. Moreover, studies have revealed that X-ray repair cross complementary gene polymorphism significantly varies between and within different ethnic groups globally. The present case-control study was aimed to investigate the association of X-ray repair cross complementary 1A (Arg194Trp) and X-ray repair cross complementary 3 (Thr241Met) polymorphism with the risk of breast cancer in females from northeastern region of India. The present case-control study includes histopathologically confirmed and newly diagnosed 464 cases with breast cancer and 534 apparently healthy neighborhood community controls. Information on sociodemographic factors and putative risk factors were collected from each study participant by conducting face-to-face interviews. Genotyping of X-ray repair cross complementary 1A (Arg194Trp) and X-ray repair cross complementary 3 (Thr241Met) was carried out by polymerase chain reaction-restriction fragment length polymorphism. For statistical analysis, both univariate and multivariate logistic regression analyses were performed. We also performed stratified analysis to find out the association of X-ray repair cross complementary genes with the risk of breast cancer stratified based on menstrual status. This study revealed that tryptophan allele (R/W-W/W genotype) in X-ray repair cross complementary 1A (Arg194Trp) gene significantly increased the risk of breast cancer (adjusted odds ratio = 1.44, 95% confidence interval = 1.06-1.97, P < .05 for R/W-W/W genotype). Moreover, it was found that tryptophan allele (W/W genotype) at codon 194 of X-ray repair cross complementary 1A (Arg194Trp) gene significantly increased the risk of breast cancer in premenopausal females (crude odds ratio = 1.66, 95% confidence interval = 1.11-2.46, P < .05 for R/W-W/W genotype). The present study did not reveal any significant association of X-ray repair cross complementary 3 (Thr241Met) polymorphism with the risk of breast cancer. The present study has explored that X-ray repair cross complementary 1A (Arg194Trp) gene polymorphism is significantly associated with the increased risk of breast cancer in premenopausal females from northeastern region of India which may be beneficial for prognostic purposes.

Indexed as

Genetic Predisposition to DiseaseAdultBreast NeoplasmsDNA-Binding ProteinsDNA RepairFemaleGenetic Association StudiesGenotypeHumansIndiaMaleMiddle AgedPolymorphism, Single NucleotidePremenopauseRisk FactorsX-ray Repair Cross Complementing Protein 1DNA-Binding ProteinsX-ray Repair Cross Complementing Protein 1X-ray repair cross complementing protein 3XRCC1 protein, humanantigenbreast cancerethnicityfood habitshypoxiameta-analysispolymorphismreproductive factors

Identifiers

PMID29332455
PMCPMC5762082
OpenAlexW2769534872

What OpenQuestion holds

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LicenceCC BY-NC
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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.