| Literature DB >> 33800431 |
Foteinos-Ioannis Dimitrakopoulos1, Georgia-Angeliki Koliou2, Vassiliki Kotoula3,4, Kyriaki Papadopoulou4, Konstantinos Markou5, Konstantinos Vlachtsis6, Nikolaos Angouridakis5, Ilias Karasmanis6, Angelos Nikolaou6, Amanda Psyrri7, Anastasios Visvikis8, Paris Kosmidis9, George Fountzilas4,10, Angelos Koutras1.
Abstract
Head and neck cancer (HNC) is a significantly heterogeneous disease and includes malignancies arising from different anatomical sites, such as nasopharyngeal cancer (NPC) and laryngeal cancer (LC). In the current study, polymorphisms located in angiogenesis- and apoptosis-related genes (VEGFA, FAS, EDNRA and NBS1) were evaluated regarding their clinical significance in HNC patients. In total, 333 HNC patients were enrolled in this study and 34 variants located on the aforementioned genes were genotyped via Sanger sequencing. LC patients, homozygous A for VEGFA rs13207351, had shorter overall survival (OS) as opposed to homozygous G (Hazard ratio (HR) = 2.06, Wald's p = 0.017) upon adjustment for age, disease stage, and surgery. Following the dominant model, LC patients carrying the A allele had a marginally significantly higher risk for death (HR = 1.72, p = 0.059). NPC patients heterozygous (CT) for FAS rs2234768 had a marginal but significantly higher risk of death compared to those with homozygosity for the T allele (HR = 2.22, p = 0.056). In conclusion, rs13207351 (VEGFA) and rs2234768 (FAS) polymorphisms seem to have prognostic significance in HNC, with VEGFA rs13207351 showing the most promise in this subgroup of LC patients.Entities:
Keywords: FAS; NBS1; SNPs; VEGFA; endothelin; head and neck cancer; nasopharyngeal cancer
Year: 2021 PMID: 33800431 PMCID: PMC7962814 DOI: 10.3390/cancers13051163
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639