Evidence map›Paper›PMID 41569203›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2026

The Genetic Polymorphisms of DNA Repair Gene RAD51 and Their Role as a Predictive Biomarker for Breast Cancer Risk and Response to Radiotherapy in Iraqi Women.

Haael Subhi Abbas, Ali Abdul Hussein Mahdi, Nihad Khalawe Tektook

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Article in Asian Pacific journal of cancer prevention : APJCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Haael Subhi AbbasDepartment of Techniques for Pathological Analysis, College of Health and Medical Techniques, Middle Technical University, Baghdad, Iraq.ORCID 0000-0002-5919-3711
Ali Abdul Hussein MahdiDepartment of Techniques for Pathological Analysis, College of Health and Medical Techniques, Middle Technical University, Baghdad, Iraq.ORCID 0000-0002-7834-6082
Nihad Khalawe TektookDepartment of Techniques for Pathological Analysis, College of Health and Medical Techniques, Middle Technical University, Baghdad, Iraq.ORCID 0000-0002-6685-627X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveVariation in the DNA repair gene RAD51 has been linked to breast cancer (BC), the most common cancer worldwide, raising concerns about radiotherapy (RT) resistance. This study aims to determine RAD51 levels and polymorphisms in Iraqi women with BC before and after RT and to evaluate their potential as cancer risk and treatment response biomarkers.

methodsThis follow-up study examined 90 blood samples from 30 newly diagnosed BC patients aged 34-56 years before and after RT at the Al-Amal National Hospital for Cancer Management in Baghdad collected from July 2024 to January 2025, and from 30 age- and sex-matched healthy controls. In ELISA, serum RAD51 levels were estimated. RAD51 SNPs were genotyped through PCR amplification with specific primers and DNA sequencing.

resultPost-RT, BC patients had significantly more RAD51 levels than pre-treatment patients and controls (2.51±0.70 vs. 1.22±0.19 vs. 1.27±0.21 ng/ml). The Iraqi population's rs1801320 (G>C) and rs1801321 (G>T) SNPs in exon 1 of the RAD51 were identified and recently registered at the NCBI (PV661827 and PV661828). The RAD51 (G>T) polymorphism's GT genotype and T allele were significant risk factors for BC (OR=11.07, CI=3.20-37.87 and OR=4.92, CI=1.82-13.35). BC patients had a lower variation post-RT compared to prior (20.0% vs. 27.0%). The RAD51 (G>C) polymorphism GC genotype or C allele was not linked with BC risk (OR=2.25, CI=0.50-9.93 and OR=2.11, CI=0.503-8.87, P>0.05).

conclusionThe Iraqi BC risk was associated with the RAD51 (G>T) polymorphism. GT genotype / T allele patients responded well to RT, indicating that RAD51 might predict cancer risk and RT effectiveness. Iraqi women may benefit from the RAD51 (G>C) GG genotype in protection against BC.

Indexed as

Biomarkers, TumorBreast NeoplasmsDNA RepairPolymorphism, Single NucleotideRad51 RecombinaseAdultCase-Control StudiesFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansIraqMiddle AgedPrognosisRisk FactorsBiomarkers, TumorRAD51 protein, humanRad51 RecombinaseBiomarkerbreast cancerpolymorphismsRAD51Radiation therapy

Identifiers

PMID41569203
PMCPMC13418024

What Socratic holds

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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 Socratic graph.