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Associations of the Rs1801133 Polymorphism with Gastric Cancer Risk in the Chinese Han Population

Overview
Journal Biomed Rep
Specialty Biochemistry
Date 2020 Dec 3
PMID 33269075
Citations 7
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Abstract

In recent years, increasing evidence has implicated the importance of mutations in the gene in the risk of gastric cancer risk. A single nucleotide polymorphism (SNP) in the gene (rs1801133) may serve a critical role in gastric cancer. A hospital-based case-controlled study was performed to assess the risk of the rs1801133 polymorphism on gastric cancer. A total of 307 patients with gastric cancer and 560 patients in the control group were recruited. Genomic DNA was extracted from peripheral blood and genotyped for rs1801133 using the ligase detection reaction. The relationship between rs1801133 and gastric cancer risk was evaluated by unconditional logistical regression analysis. The rs1801133-TT genotype was associated with a borderline significantly decreased risk of gastric cancer [(TT vs. CC, adjusted odds ratio (OR)=0.54, 95% confidence intervals (CI)=0.35-0.83; P=0.006; CT vs. CC, adjusted OR=0.59, 95% CI=0.44-0.79, P<0.001; and TT/CT vs. CC, adjusted OR=0.61, 95% CI=0.44-0.83, P=0.001), and further analysis showed the relationship was evident amongst older patients and patients who never drank alcohol. The C>T mutation at rs1801133 of the gene was associated with a decreased risk of gastric cancer in older individuals and those who never drink.

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References
1.
Vidmar Golja M, Smid A, Kuzelicki N, Trontelj J, Gersak K, Mlinaric-Rascan I . Folate Insufficiency Due to MTHFR Deficiency Is Bypassed by 5-Methyltetrahydrofolate. J Clin Med. 2020; 9(9). PMC: 7564482. DOI: 10.3390/jcm9092836. View

2.
Custodio A, Moreno-Rubio J, Aparicio J, Gallego-Plazas J, Yaya R, Maurel J . Pharmacogenetic predictors of outcome in patients with stage II and III colon cancer treated with oxaliplatin and fluoropyrimidine-based adjuvant chemotherapy. Mol Cancer Ther. 2014; 13(9):2226-37. DOI: 10.1158/1535-7163.MCT-13-1109. View

3.
Liew S, Das Gupta E . Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism: epidemiology, metabolism and the associated diseases. Eur J Med Genet. 2014; 58(1):1-10. DOI: 10.1016/j.ejmg.2014.10.004. View

4.
Jain M, Pandey P, Tiwary N, Jain S . MTHFR C677T polymorphism is associated with hyperlipidemia in women with polycystic ovary syndrome. J Hum Reprod Sci. 2012; 5(1):52-6. PMC: 3409921. DOI: 10.4103/0974-1208.97802. View

5.
Wang W, Sun Z, Deng J, Qi X, Feng X, Fang C . A novel nomogram individually predicting disease-specific survival after D2 gastrectomy for advanced gastric cancer. Cancer Commun (Lond). 2018; 38(1):23. PMC: 5993138. DOI: 10.1186/s40880-018-0293-0. View