Department of Haematology, Toxicology, Radiation, and Occupation, 103 Military Hospital, Vietnam Military Medical University, Hanoi, Vietnam.
The Center of Toxicological and Radiological Training and Research, Vietnam Military Medical University, Hanoi, Vietnam.
Sci Rep. 2024 Feb 9;14(1):3315. doi: 10.1038/s41598-024-54004-0.
Among the congener of dioxin, 2,3,7,8-TCDD is the most toxic, having a serious long-term impact on the environment and human health. UDP-glucuronosyltransferase 1A1 (UGT1A1) plays a crucial role in the detoxification and excretion of endogenous and exogenous lipophilic compounds, primarily in the liver and gastrointestinal tract. This study aimed to investigate the association of UGT1A1 gene polymorphisms, expression levels, and enzyme concentration with Agent Orange/Dioxin exposure. The study included 100 individuals exposed to Agent Orange/Dioxin nearby Da Nang and Bien Hoa airports in Vietnam and 100 healthy controls. UGT1A1 SNP rs10929303, rs1042640 and rs8330 were determined by Sanger sequencing, mRNA expression was quantified by RT-qPCR and plasma UGT1A1 concentrations were measured by ELISA. The results showed that UGT1A1 polymorphisms at SNPs rs10929303, rs1042640 and rs8330 were associated with Agent Orange/Dioxin exposure (OR = 0.55, P = 0.018; OR = 0.55, P = 0.018 and OR = 0.57, P = 0.026, respectively). UGT1A1 mRNA expression levels and enzyme concentration were significantly elevated in individuals exposed to Agent Orange/Dioxin compared to controls (P < 0.0001). Benchmark dose (BMD) analyses showed that chronic exposure to 2,3,7,8-TCDD contamination affects the UGT1A1 mRNA and protein levels. Furthermore, UGT1A1 polymorphisms affected gene expression and enzyme concentrations in individuals exposed to Agent Orange/Dioxin. In conclusion, UGT1A1 gene polymorphisms, UGT1A gene expression levels and UGT1A1 enzyme concentrations were associated with Agent Orange/Dioxin exposure. The metabolism of 2,3,7,8-TCDD may influence UGT1A gene expression and enzyme concentrations.
在二恶英同系物中,2,3,7,8-四氯二苯并对二恶英(TCDD)的毒性最强,对环境和人类健康有严重的长期影响。尿苷二磷酸葡萄糖醛酸转移酶 1A1(UGT1A1)在解毒和排泄内源性和外源性亲脂性化合物方面发挥着关键作用,主要在肝脏和胃肠道中。本研究旨在探讨 UGT1A1 基因多态性、表达水平和酶浓度与接触橘剂/二恶英的关系。研究纳入了 100 名在越南岘港和边和机场附近接触过橘剂/二恶英的个体和 100 名健康对照者。通过 Sanger 测序确定 UGT1A1 SNP rs10929303、rs1042640 和 rs8330,通过 RT-qPCR 定量 mRNA 表达,通过 ELISA 测量血浆 UGT1A1 浓度。结果表明,UGT1A1 在 SNPs rs10929303、rs1042640 和 rs8330 上的多态性与接触橘剂/二恶英有关(OR=0.55,P=0.018;OR=0.55,P=0.018 和 OR=0.57,P=0.026)。与对照组相比,接触过橘剂/二恶英的个体 UGT1A1 mRNA 表达水平和酶浓度显著升高(P<0.0001)。基准剂量(BMD)分析表明,慢性接触 2,3,7,8-TCDD 污染会影响 UGT1A1 的 mRNA 和蛋白水平。此外,UGT1A1 多态性影响接触过橘剂/二恶英个体的基因表达和酶浓度。综上所述,UGT1A1 基因多态性、UGT1A 基因表达水平和 UGT1A1 酶浓度与接触橘剂/二恶英有关。2,3,7,8-TCDD 的代谢可能会影响 UGT1A 基因表达和酶浓度。