Evidence map›Paper›PMID 41312940›Full record

SynthesisAsian Pacific journal of cancer prevention : APJCP2025

XRCC1 Arg399Gln Genetic Variant Increases Colorectal Cancer Susceptibility: A Comprehensive Meta-Analysis.

Praveen Kumar Kampalli, Mohan Krishna Ghanta, Rishitha Chowdary Mavillapalli, Afroz Alam, Sujatha Peela, Lvks Bhaskar

Abstract readMeta-Analysis
In one paragraph

Synthesis in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Praveen Kumar KampalliDepartment of Bioscience & Biotechnology, Banasthali University, Rajasthan, India.
Mohan Krishna GhantaDepartment of Pharmacology, MVJ Medical College and Research Hospital, Bangalore-562114, Karnataka, India.
Rishitha Chowdary MavillapalliDepartment of Mutagenicity & Genetic Toxicology, Adgyl Life Sciences, Eurofins Advinus, Shameerpet - 500078, Telangana, India.
Afroz AlamDepartment of Bioscience & Biotechnology, Banasthali University, Rajasthan, India.
Sujatha PeelaDepartment of Biotechnology, Dr.B.R.Ambedkar University, Srikakulam, India.
Lvks BhaskarDepartment of Zoology, Guru Ghasidas Vishwavidyalaya, Bilaspur, Chhattisgarh-495009, India.ORCID 0000-0003-2977-6454

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionColorectal cancer (CRC) continues to be a common health condition and one of the most prevalent and lethal  cancers worldwide. CRC is the third most leading cancer by incidence and second most common cause of cancer mortality. Emerging evidence showing that inherited genetic variants in genes coding for DNA repair enzymes have potential role in increasing the risk of CRC. Among these,  polymorphisms in the XRCC1 has been widely investigated, although the results have been varied in different populations.

methodsThe current meta-analysis is aimed to explain the relation between three XRCC1 polymorphisms and the CRC risk. Meta-analysis included a combined analysis of 52 case-controls studies including 23 Arg194Trp studies, 8 Arg280His studies, and 42 Arg399Gln studies.

resultsThe results of the present study revealed a statistically significant correlation between the Arg399Gln polymorphism and the increased risk of CRC (OR = 1.10, 95% CI = 1.01-1.20, p = 0.038, random effects model). However, subgroup analysis based on ethnicity revealed no statistical significance between CRC risk and XRCC1 polymorphisms in Asian and Caucasian populations. In addition, no publication bias was found in the current meta-analysis.

conclusionOverall, the data suggest that XRCC1 Arg399Gln might be associated with increased CRC susceptibility, while Arg194Trp and Arg280His are not significantly associated.

Indexed as

Colorectal NeoplasmsDNA-Binding ProteinsGenetic Predisposition to DiseasePolymorphism, GeneticPolymorphism, Single NucleotideCase-Control StudiesHumansPrognosisRisk FactorsX-ray Repair Cross Complementing Protein 1DNA-Binding ProteinsX-ray Repair Cross Complementing Protein 1XRCC1 protein, humancolorectal cancerGeneMeta-analysisSNPXRCC1

Identifiers

PMID41312940
PMCPMC12948178

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.