Evidence map›Paper›PMID 39560804›Full record

ArticleMolecular biology reports2024

Association between the variations in metabolic pathways and oral cancer risk: results from a Pakistani case-control study.

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

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Arifa ShabbirDepartment of Zoology, GC University, Lahore, Pakistan.
Muhammad Usman RashidDepartment of Basic Sciences Research, Shaukat Khanum Memorial Cancer Hospital and Research Centre (SKMCH&RC), 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.
Naila MalkaniDepartment of Zoology, GC University, Lahore, Pakistan. nailamalkani@gcu.edu.pk.ORCID https://orcid.org/0000-0001-6454-1525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOral cancer (OC) is a significant global health concern, with Pakistan ranking 5th worldwide in OC incidence. Given the poor prognosis, early detection of at-risk individuals is crucial. Genetic factors, particularly single nucleotide polymorphisms (SNPs) in metabolic genes, may influence OC susceptibility. This study investigated the association between SNPs in CYP1A1, COX2, SOD2, and HIF1a genes and OC risk in the Pakistani population.

methodsA prospective study was conducted from October 2019 to March 2022, enrolling 215 newly diagnosed OC patients and 410 controls. Genetic variations were analyzed using High-Resolution Melting (HRM) analysis and Sanger sequencing, with protein expression evaluated by ELISA.

resultsNo significant associations were found between the studied SNPs and OC risk. However, a non-significant trend was observed for the SOD2 variant (rs4880), where the G allele was associated with a higher OC risk than the A allele (p = 0.20). Elevated COX2 and HIF1α levels (p-values of 0.014 and < 0.001, respectively) and reduced SOD2 levels (p < 0.0001) were observed in OC patients, while CYP1A1 levels remained similar in both controls and cases.

conclusionAlthough SNPs in CYP1A1, COX2, SOD2, and HIF1α were not significantly associated with OC risk in the Pakistani population, altered protein expression levels of COX2, HIF1α and SOD2 suggest additional regulatory mechanisms. Further investigation into post-transcriptional modifications and epigenetic factors could lead to novel biomarkers and therapeutic targets for OC in Pakistan.

Indexed as

Cytochrome P-450 CYP1A1Genetic Predisposition to DiseaseHypoxia-Inducible Factor 1, alpha SubunitMouth NeoplasmsPolymorphism, Single NucleotideSuperoxide DismutaseAdultAgedAllelesCase-Control StudiesCyclooxygenase 2FemaleHumansMaleMetabolic Networks and PathwaysMiddle AgedCyclooxygenase 2CYP1A1 protein, humanCytochrome P-450 CYP1A1HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitPTGS2 protein, humanSuperoxide DismutaseSuperoxide Dismutase 2COX2CYP1A1HIF1αOral cancerSingle nucleotide polymorphismSOD2

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