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ArticleMolecular biology reports2025

Association of PD-1 immune checkpoint polymorphisms with oral cancer risk: results from a Pakistani case-control study.

Iqra Mubeen, Arifa Shabbir, Ezzat M Awad, Humaira Naeemi, Talin Barisani-Asenbauer, Muhammad Usman Rashid, Naila Malkani

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Article in Molecular biology reports, 2025. 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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7 authors.

Iqra MubeenDepartment of Zoology, GC University, Lahore, Pakistan.
Arifa ShabbirDepartment of Zoology, GC University, Lahore, Pakistan.
Ezzat M AwadDepartment of Ophthalmology & Optometry, Medical University Vienna, Vienna, Austria.
Humaira NaeemiDepartment of Basic Sciences Research, Shaukat Khanum Memorial Cancer Hospital and Research Centre (SKMCH&RC), Lahore, Pakistan.
Talin Barisani-AsenbauerDepartment of Ophthalmology & Optometry, Medical University Vienna, Vienna, Austria.
Muhammad Usman RashidDepartment of Basic Sciences Research, Shaukat Khanum Memorial Cancer Hospital and Research Centre (SKMCH&RC), Lahore, Pakistan.
Naila MalkaniDepartment of Zoology, GC University, Lahore, Pakistan. nailamalkani@gcu.edu.pk.ORCID http://orcid.org/0000-0001-6454-1525

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6 · The paper itself

Abstract

backgroundOral Cancer (OC) is a major public health concern in Pakistan, ranking as the leading cause of cancer-related mortality in males and a significant contributor in females. Genetic variations, predominantly single nucleotide polymorphisms (SNPs) in immune checkpoint genes, are implicated in OC susceptibility. However, their role remains unclear. This study investigates PD-1 gene polymorphisms and their association with OC risk in the Pakistani population. METHODOLOGY: A case-control study was conducted from 2019 to 2022, recruiting 215 OC cases and 411 healthy controls for genetic analysis. High-Resolution Melting (HRM) analysis and Sanger sequencing were used for genotyping rs36084323 and rs2227981, while ELISA was performed to evaluate PD-1 protein expression levels.

resultsGenotypic analysis revealed a significant association between rs36084323 and OC susceptibility (p = 0.02; OR = 1.99; 95% CI = 1.09-3.61), particularly in individuals carrying the CC and CT genotypes. However, rs2227981 showed no significant association. Haplotype analysis indicated that the CG haplotype (p = 0.004; OR = 1.68; 95% CI = 1.18-2.39) was significantly associated with higher OC risk, while the AG haplotype (p = 0.02; OR = 0.52; 95% CI = 0.29-0.94) was linked to a protective effect. PD-1 protein expression levels did not differ between cases and controls.

conclusionThe PD-1 rs36084323 polymorphism may serve as a genetic biomarker for OC susceptibility in Pakistan, emphasizing the need for targeted genetic screening and early detection strategies. Further research could uncover novel biomarkers and therapeutic targets for OC in the Pakistani population.

Indexed as

Mouth NeoplasmsProgrammed Cell Death 1 ReceptorAdultAgedCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMaleMiddle AgedPakistanPolymorphism, Single NucleotideRisk FactorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorHigh resolution melt curveOral cancerPakistani populationPD-1 polymorphism

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