PMID- 31781300 OWN - NLM STAT- MEDLINE DCOM- 20200427 LR - 20220411 IS - 1875-8630 (Electronic) IS - 0278-0240 (Print) IS - 0278-0240 (Linking) VI - 2019 DP - 2019 TI - Determination of SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, and RAGE rs1800625 Single Gene Polymorphisms in Patients with Laryngeal Squamous Cell Carcinoma. PG - 3907232 LID - 10.1155/2019/3907232 [doi] LID - 3907232 AB - PURPOSE: To determine the frequency of the genotype of signal transducer and activator of transcription protein 3 (STAT3) rs744166, sirtuin (SIRT1) rs12778366, fibroblast growth factor (FGFR2) rs2981582, and advanced glycosylation end product-specific receptor (RAGE) rs1800625 gene polymorphisms in patients with laryngeal squamous cell carcinoma (LSCC). METHODS: A total of 944 subjects were evaluated, which includes 144 patients with LSCC and 800 healthy controls. The genotyping of STAT3 rs744166, SIRT1 rs12778366, FGFR2 rs2981582, and RAGE rs1800625 was carried out using the RT-PCR. RESULTS: The analysis of STAT3 rs744166, SIRT1 rs12778366, and FGFR2 rs2981582 gene polymorphisms did not reveal any differences in genotype distribution between the patients with LSCC and the control subjects. However, statistical analysis revealed that genotypes (AA, AG, and GG) of rs1800625 in RAGE gene were distributed statistically significantly differently between patients and controls (61.1%, 30.6%, and 23.6% vs. 72.5%, 25.8%, and 1.8%, respectively; p < 0.001). Additionally, statistical significance was observed in allele distribution between these two groups, i.e., allele G at rs1800625 was more frequently observed in the patient group than in controls (23.6% vs. 14.6%; p < 0.001). CONCLUSION: RAGE rs1800625 gene polymorphism may play a significant role in laryngeal squamous cell carcinoma development. CI - Copyright (c) 2019 Virgilijus Uloza et al. FAU - Uloza, Virgilijus AU - Uloza V AD - Department of Otolaryngology, Academy of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Tamauskaite, Toma AU - Tamauskaite T AD - Academy of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Vilkeviciute, Alvita AU - Vilkeviciute A AUID- ORCID: 0000-0002-0427-5568 AD - Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Pasvenskaite, Agne AU - Pasvenskaite A AD - Department of Otolaryngology, Academy of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Liutkevicius, Vykintas AU - Liutkevicius V AUID- ORCID: 0000-0002-7349-4844 AD - Department of Otolaryngology, Academy of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Liutkeviciene, Rasa AU - Liutkeviciene R AUID- ORCID: 0000-0001-5395-923X AD - Neuroscience Institute, Lithuanian University of Health Sciences, Kaunas, Lithuania. LA - eng PT - Journal Article DEP - 20191112 PL - United States TA - Dis Markers JT - Disease markers JID - 8604127 RN - 0 (Antigens, Neoplasm) RN - 0 (Biomarkers, Tumor) RN - 0 (STAT3 Transcription Factor) RN - 0 (STAT3 protein, human) RN - EC 2.7.10.1 (FGFR2 protein, human) RN - EC 2.7.10.1 (Receptor, Fibroblast Growth Factor, Type 2) RN - EC 2.7.11.22 (MOK protein, human) RN - EC 2.7.11.24 (Mitogen-Activated Protein Kinases) RN - EC 3.5.1.- (SIRT1 protein, human) RN - EC 3.5.1.- (Sirtuin 1) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Antigens, Neoplasm/*genetics MH - Biomarkers, Tumor/genetics MH - Carcinoma, Squamous Cell/*genetics/pathology MH - Case-Control Studies MH - Female MH - Follow-Up Studies MH - Genetic Predisposition to Disease MH - Genotype MH - Humans MH - Laryngeal Neoplasms/*genetics/pathology MH - Male MH - Middle Aged MH - Mitogen-Activated Protein Kinases/*genetics MH - *Polymorphism, Single Nucleotide MH - Prognosis MH - Receptor, Fibroblast Growth Factor, Type 2/*genetics MH - STAT3 Transcription Factor/*genetics MH - Sirtuin 1/*genetics MH - Young Adult PMC - PMC6875326 COIS- None of the authors has any proprietary interests or conflicts of interest related to this submission. EDAT- 2019/11/30 06:00 MHDA- 2020/04/28 06:00 PMCR- 2019/11/12 CRDT- 2019/11/30 06:00 PHST- 2019/04/07 00:00 [received] PHST- 2019/09/28 00:00 [accepted] PHST- 2019/11/30 06:00 [entrez] PHST- 2019/11/30 06:00 [pubmed] PHST- 2020/04/28 06:00 [medline] PHST- 2019/11/12 00:00 [pmc-release] AID - 10.1155/2019/3907232 [doi] PST - epublish SO - Dis Markers. 2019 Nov 12;2019:3907232. doi: 10.1155/2019/3907232. eCollection 2019.