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Combined impacts of histamine receptor H1 gene polymorphisms and an environmental carcinogen on the susceptibility to and progression of oral squamous cell carcinoma

Oral squamous cell carcinoma (OSCC) is the most frequently encountered type of oral cancer. Histamine receptor H1 ( ) was reported to play a crucial role in OSCC carcinogenesis, but impacts of genetic variants of on OSCC remain unclear. Herein, we investigated the association between functional sing...

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Published in:Aging (Albany, NY.) NY.), 2022-05, Vol.14 (undefined), p.4500-4512
Main Authors: Ding, Yi-Fang, Lin, Yung-Wei, Chiu, Wen-Kuan, Lin, Chiao-Wen, Yang, Yi-Chieh, Chang, Lun-Ching, Chang, Jungshan, Yang, Shun-Fa, Chien, Ming-Hsien
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Language:English
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Summary:Oral squamous cell carcinoma (OSCC) is the most frequently encountered type of oral cancer. Histamine receptor H1 ( ) was reported to play a crucial role in OSCC carcinogenesis, but impacts of genetic variants of on OSCC remain unclear. Herein, we investigated the association between functional single-nucleotide polymorphisms (SNPs) of and OSCC susceptibility or clinicopathologic variables by logistic regression models. genotypes at four loci (rs346074, rs346076, rs901865, and rs2606731) were analyzed by a TaqMan allelic discrimination assay, and we found that patients harboring rs901865 T and rs346074 T alleles had a significantly lower risk of developing larger tumor sizes (>T2) under a dominant model. Based on the environmental carcinogen exposure status, we observed that rs901865 polymorphic variants were also associated with a lower risk of developing more-advanced clinical stages (III or IV) in patients with a betel-quid-chewing habit. Moreover, genotype screening of rs901865 and rs346074 in OSCC cell lines showed that cells respectively carrying the CT and TT genotypes expressed lower HRH1 levels compared to cells carrying the CC genotype of rs901865 and rs346074. Furthermore, analyses of TCGA and GEO databases revealed that expression levels were upregulated in head and neck squamous cell carcinoma (HNSCC) and OSCC tissues compared to normal tissues and were correlated with larger tumor sizes and poorer prognoses. These results indicated the involvement of SNPs rs901865 and rs346074 in OSCC development and support the interaction between gene polymorphisms and an environmental carcinogen as a predisposing factor for OSCC progression.
ISSN:1945-4589
1945-4589
DOI:10.18632/aging.204089