Genetic Variants in One-carbon Metabolism-related Genes Contribute to NSCLC Prognosis in a Chinese Population
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Background: One-carbon metabolism plays a critical role in DNA methylation and DNA synthesis. Variants of genes involved in one-carbon metabolism may result in aberrant methylation and/or DNA synthesis inhibition, and ultimately modulate the initiation and progression of tumors. In this study, the authors hypothesized that polymorphisms in one-carbon metabolism-related genes may contribute to the prognosis of nonsmall cell lung cancer (NSCLC).
Methods: The authors screened 57 potentially functional single nucleotide polymorphisms (SNPs) from 11 candidate genes involved in one-carbon metabolism and genotyped them in a cohort of 568 NSCLC patients by using Illumina Golden Gate platform. The Kaplan-Meier method with log-rank test and Cox proportional hazards model were used for survival analyses.
Results: Variant alleles were significantly associated with favorable survivals of NSCLC for MTR rs3768160 A>G (allelic hazards ratio [HR], 0.78; 95% confidence interval [CI], 0.62-0.98), MTRR rs2966952 G>A (allelic HR, 0.84; 95% CI, 0.71-0.99) and DHFR rs1650697 G>A (allelic HR, 0.83; 95% CI, 0.70-0.99) and with unfavorable prognosis for MTHFD1 rs1950902 G>A with borderline significance (allelic HR, 1.18; 95% CI, 0.99-1.40). In addition, the combined genotypes of these four SNPs showed a locus-dosage effect on NSCLC survival (P(trend) = 6.9 × 10(-5) ). In the final multivariate Cox regression model, combined genotypes based on 3 categories may be an independent prognostic factor for NSCLC with adjusted trend HR of 0.78 (95% CI, 0.66-0.92).
Conclusion: Genetic variants in one-carbon metabolism pathway may be candidate biomarkers for NSCLC prognosis.
Zhou L, Li Q, Xu J, Wang S, Song Z, Chen X Neurooncol Adv. 2023; 5(1):vdac181.
PMID: 36879663 PMC: 9985165. DOI: 10.1093/noajnl/vdac181.
GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL.
Takashima Y, Hamano M, Fukai J, Iwadate Y, Kajiwara K, Kobayashi T Sci Rep. 2020; 10(1):8435.
PMID: 32439996 PMC: 7242340. DOI: 10.1038/s41598-020-65463-6.
Hayano A, Takashima Y, Yamanaka R Int J Clin Oncol. 2019; 24(9):1020-1029.
PMID: 30993483 DOI: 10.1007/s10147-019-01451-9.
Chen K, Liu H, Liu Z, Luo S, Patz Jr E, Moorman P Int J Cancer. 2019; 145(3):621-631.
PMID: 30650190 PMC: 6828159. DOI: 10.1002/ijc.32128.
Ding K, Jiang J, Chen L, Xu X Med Sci Monit. 2018; 24:7499-7507.
PMID: 30343310 PMC: 6206813. DOI: 10.12659/MSM.910265.