Interactions between alcohol consumption and xenobiotic metabolism SNPs in HNSCC risk: insights from a systematic review

Background: Head and Neck Squamous Cell Carcinoma (HNSCC) is the sixth most predominant cancer worldwide, with a poor prognosis and low survival rate. Alcohol consumption is a well-established environmental risk factor, despite other environmental and genetic risk factors having also been implicated [1,2,3]. Considering the role that xenobiotic metabolizing enzymes play in alcohol metabolism, it is likely that the interplay between these factors contributes significantly to the development of HNSCC. Objective: The aim of this work was to identify gene-environment interactions (GxE) involving alcohol consumption and Single Nucleotide Polymorphisms (SNPs) in xenobiotic metabolism genes, previously associated with HNSCC risk, through a systematic review of the scientific literature. Methods: The systematic review was registered in the PROSPERO database and conducted according to PRISMA guidelines and PICO criteria. PubMed, Scopus and Web of Science were searched using an expression combining both MeSH and common language terms. Rayyan was used to remove duplicates and select the studies according to the predefined inclusion and exclusion criteria. All relevant data from selected articles were extracted into an Excel datasheet to be further analyzed. Results: Most GxE interactions with alcohol consumption involved SNPs in Cytochrome P450 genes SNPs (mainly CYP1A1, CYP1B1 and CYP2E1), where replicated results were observed among different studies. SNPs in other phase I enzymes, such as ADH1B, ADH1C and ALDH2, and phase II enzymes, such as GSTM1, were also strongly implicated. Isolated significant findings were observed in additional SNPs, but with less conclusive evidence. Conclusions: Alcohol consumption interacts with xenobiotic metabolism SNPs, mainly through Phase I enzymes, to increase HNSCC risk. Further studies in larger populations of different origins are needed in order to confirm these findings and expand current knowledge on this important subject.

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Publication Details

Journal
Science Letters
Published
2026-04-14
DOI
https://doi.org/10.48797/sl.2026.425
Primary Topic
Glutathione Transferases and Polymorphisms
Type
article
Field-Weighted Citation Impact
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article

Interactions between alcohol consumption and xenobiotic metabolism SNPs in HNSCC risk: insights from a systematic review

Raquel M. Silva, Luís Silva Santos, Mateus Monteiro
Science Letters
Glutathione Transferases and Polymorphisms
article

Interactions between alcohol consumption and xenobiotic metabolism SNPs in HNSCC risk: insights from a systematic review

Raquel M. Silva, Luís Silva Santos, Mateus Monteiro
article en

Abstract

Background: Head and Neck Squamous Cell Carcinoma (HNSCC) is the sixth most predominant cancer worldwide, with a poor prognosis and low survival rate. Alcohol consumption is a well-established environmental risk factor, despite other environmental and genetic risk factors having also been implicated [1,2,3]. Considering the role that xenobiotic metabolizing enzymes play in alcohol metabolism, it is likely that the interplay between these factors contributes significantly to the development of HNSCC. Objective: The aim of this work was to identify gene-environment interactions (GxE) involving alcohol consumption and Single Nucleotide Polymorphisms (SNPs) in xenobiotic metabolism genes, previously associated with HNSCC risk, through a systematic review of the scientific literature. Methods: The systematic review was registered in the PROSPERO database and conducted according to PRISMA guidelines and PICO criteria. PubMed, Scopus and Web of Science were searched using an expression combining both MeSH and common language terms. Rayyan was used to remove duplicates and select the studies according to the predefined inclusion and exclusion criteria. All relevant data from selected articles were extracted into an Excel datasheet to be further analyzed. Results: Most GxE interactions with alcohol consumption involved SNPs in Cytochrome P450 genes SNPs (mainly CYP1A1, CYP1B1 and CYP2E1), where replicated results were observed among different studies. SNPs in other phase I enzymes, such as ADH1B, ADH1C and ALDH2, and phase II enzymes, such as GSTM1, were also strongly implicated. Isolated significant findings were observed in additional SNPs, but with less conclusive evidence. Conclusions: Alcohol consumption interacts with xenobiotic metabolism SNPs, mainly through Phase I enzymes, to increase HNSCC risk. Further studies in larger populations of different origins are needed in order to confirm these findings and expand current knowledge on this important subject.

Science Letters
Reduced inequalities
Openalex Percentile: Top 9%
Glutathione Transferases and Polymorphisms
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