Evidence map›Paper›PMID 41660933›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2026

Four Gene Polymorphisms as Potential Predictive Biomarkers for Lung Cancer Susceptibility and Therapeutic Response in Iraqi Patients: A Pharmacogenetic Case-Control Study.

Mohammed Ouda Orabiy, Doaa Hadi Chyad, Wisam Hindawi Hoidy

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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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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mohammed Ouda OrabiyMinistry of Education, General Directorate of Al-Qadisiyah Education, Al-Diwaniyah City, Iraq.
Doaa Hadi ChyadMinistry of Education, General Directorate of Al-Qadisiyah Education, Al-Diwaniyah City, Iraq.
Wisam Hindawi HoidyDepartment of Chemistry, College of Education, University of Al-Qadisiyah, Al-Diwaniyah City, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer remains the leading cause of cancer-related deaths worldwide, with limited genetic data available on Middle Eastern populations. This study investigated four novel genetic variants CYPHER rs7834621, METOX1 rs9284659, DRUGRES2 rs4521739, and TOXMET3 rs8823471 for their association with lung cancer risk and treatment response in Iraqi patients.

methodsBetween January 2024 and September 2024, we recruited 265 tissue-confirmed lung cancer patients and 310 healthy controls from Al-Diwaniyah Teaching Hospital. DNA was extracted from blood samples and genotyped using tetra-ARMS-PCR. Logistic regression was used to analyze variant-cancer risk associations. Pharmacogenetic analysis included 198 patients receiving trastuzumab, doxorubicin, paclitaxel, and cyclophosphamide chemotherapy, with response measured by RECIST criteria.

resultsAll four genetic variants showed significant associations with lung cancer risk. The CYPHER rs7834621 GG genotype was associated with the highest disease risk (adjusted OR = 2.21, 95% CI: 1.31-3.73, p = 0.003). Allele frequencies were population-specific when compared to other cohorts. Pharmacogenetic analysis revealed treatment response associations, with DRUGRES2 rs4521739 TT genotype demonstrating superior response rates compared to CC genotype (68.4% vs 31.6%, p < 0.001). Haplotype analysis identified specific gene combinations that increased disease susceptibility.

conclusionsThese novel SNPs are associated with both lung cancer risk and treatment response in Iraqi patients, potentially serving as biomarkers for risk stratification and personalized therapy guidance in this population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorGenetic Predisposition to DiseaseLung NeoplasmsPolymorphism, Single NucleotideAdultAgedCase-Control StudiesFemaleFollow-Up StudiesHumansIraqMaleMiddle AgedPrognosisBiomarkers, Tumorgene polymorphismsLung cancerPersonalized Medicinepharmacogenetics -tetra-ARMS PCR

Identifiers

PMID41660933
PMCPMC13499589

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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.