García-García Carlos Abraham, Cruz-Gregorio Alfredo, Pedraza-Chaverri José, Montaño Luis F, Rendón-Huerta Erika P
Laboratorio de Inmunobiología, Departamento de Biología Celular y Tisular, Facultad de Medicina, UNAM, Mexico.
Departamento de Fisiología, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico.
Toxicol In Vitro. 2025 Jan;102:105952. doi: 10.1016/j.tiv.2024.105952. Epub 2024 Oct 10.
Carcinogenic N-nitroso compounds, especially N-nitroso dimethylamine, increase the risk of gastric cancer development. Cytochrome P450-2E1 metabolizes this compound, thus generating an oxidant microenvironment. We aimed to evaluate in gastric adenocarcinoma cells if its effect on CYP2E1 and ROS affects signaling pathways associated with gastric cancer oncogenesis. The impact of N- nitroso dimethylamine upon CYP2E1 and ROS activation/secretion was evaluated by the DCFDA assay protocol, TER measurements, Stat3, pSTAT3, ERK1/2, and pERK1/2 expression, claudins-1 and -6 expression, and finally mRNA values of IL-1β IL-6, IL-8 and TNFα. Our results showed that exposure to N- N-nitroso dimethylamine disrupts the regulation of Stat3 and Erk1/2, alters the expression of claudin-1 and claudin-6 tight junction proteins, and increases the secretion of pro-inflammatory cytokines. These alterations induce a continuous local inflammatory process, an event identified as a gastric cancer promoter. In summary, N-nitroso dimethylamine can disrupt cell mechanisms associated with gastric cancer oncogenesis.
致癌性N-亚硝基化合物,尤其是N-亚硝基二甲胺,会增加患胃癌的风险。细胞色素P450-2E1可代谢这种化合物,从而产生氧化微环境。我们旨在评估在胃腺癌细胞中,其对CYP2E1和活性氧(ROS)的影响是否会影响与胃癌发生相关的信号通路。通过DCFDA检测方案、跨上皮电阻(TER)测量、信号转导和转录激活因子3(Stat3)、磷酸化信号转导和转录激活因子3(pSTAT3)、细胞外信号调节激酶1/2(ERK1/2)和磷酸化细胞外信号调节激酶1/2(pERK1/2)表达、闭合蛋白-1和闭合蛋白-6表达,以及最后白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)和肿瘤坏死因子α(TNFα)的mRNA值,评估N-亚硝基二甲胺对CYP2E1和ROS激活/分泌的影响。我们的结果表明,暴露于N-亚硝基二甲胺会破坏Stat3和Erk1/2的调节,改变闭合蛋白-1和闭合蛋白-6紧密连接蛋白的表达,并增加促炎细胞因子的分泌。这些改变会引发持续的局部炎症过程,这一事件被确定为胃癌促进因子。总之,N-亚硝基二甲胺会破坏与胃癌发生相关的细胞机制。