J. Kabziński, Monika Gogolewska, M. Nowakowski, E. Kucharska, Ł. Dziki, M. Mik, A. Dziki, I. Majsterek
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引用次数: 2
摘要
导读:尽管在诊断和治疗方面进行了大量的研究,结直肠癌(CRC)仍然是波兰死亡率第二高的癌症。导致结直肠癌高风险的因素之一可能是负责外源性代谢的蛋白质有效性的个体差异-似乎去除潜在有害的外源性物质可显着降低致癌风险。目的:本研究分析外源药物代谢相关基因多态性对结直肠癌发病风险的影响——N AT 1基因rs72554606多态性、N AT 2基因rs1799930多态性和CYP1A1基因rs1799814多态性及其表达水平。结论:结果提示NAT1的GC基因型和CYP1A1的GA基因型可增加结直肠癌的发生风险,且在已诊断为结直肠癌的人群中,NAT1的表达水平明显低于对照组。我们认为这些因素可能对结直肠癌的治疗具有潜在的预后和诊断意义。
Polymorphism association of NIL1, NIL2, CYP1A1 xenobiotic metabolism genes and their expression with the risk of colorectal cancer in the Polish population.
Introduction: Colorectal cancer (CRC), despite intensive research on the improvement of diagnosis and treatment, is still the second most deadly cancer in Poland in terms of mortality. One of the factors predisposing to a higher risk of CRC may be the individual differences in the effectiveness of proteins responsible for the metabolism of xenobiotics - it seems that the removal of potentially harmful exogenous substances significantly reduces the risk of carcinogenesis. Aim: In this work, we analyzed the effect of polymorphisms of genes responsible for metabolizing xenobiotics on the risk of CRC - rs72554606 polymorphism of N AT 1 gene, rs1799930 polymorphism of N AT 2 gene and rs1799814 polymorphism of CYP1A1 gene, as well as the level of expression of these genes. Conclusions: The results indicate that the GC genotype for N AT 1 and the GA genotype for CYP1A1 may increase the risk of CRC, and in those already diagnosed with colorectal cancer, the expression level of NAT1 is significantly lower than in the control. We believe that these factors may have potential prognostic and diagnostic significance in the treatment of CRC.