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新兴污染物与药物混合物对与毒性、氧化应激和癌症相关生物标志物调节的影响。

Effects of Mixtures of Emerging Pollutants and Drugs on Modulation of Biomarkers Related to Toxicity, Oxidative Stress, and Cancer.

作者信息

Manuguerra Simona, Carli Fabrizia, Scoditti Egeria, Santulli Andrea, Gastaldelli Amalia, Messina Concetta Maria

机构信息

Laboratory of Marine Biochemistry and Ecotoxicology, Department of Earth and Marine Sciences DiSTeM, University of Palermo, Via G. Barlotta 4, 91100 Trapani, Italy.

Institute of Clinical Physiology, National Research Council, 56124 Pisa, Italy.

出版信息

Metabolites. 2024 Oct 17;14(10):559. doi: 10.3390/metabo14100559.

Abstract

Over time, the scientific community has developed a growing interest in the effects of mixtures of different compounds, for which there is currently no established evidence or knowledge, in relation to certain categories of xenobiotics. It is well known that exposure to pollutants causes oxidative stress, resulting in the overproduction of reactive oxygen species (ROS), which can affect signaling pathways that regulate the cell cycle, apoptosis, energy balance, and cellular metabolism. The aim of this study was to investigate the effects of sub-lethal concentrations of mixtures of emerging pollutants and pharmaceuticals on the modulation of biomarkers related to toxicity, oxidative stress, and cancer. In this study, the hepatoma cell line HepG2 was exposed to increasing concentrations of polybrominated diphenyl ether 47 (BDE-47), cadmium chloride (CdCl), and carbamazepine (CBZ), both individually and in mixtures, for 72 h to assess cytotoxicity using the MTT assay. The subsequent step, following the identification of the sub-lethal concentration, was to investigate the effects of exposure at the gene expression level, through the evaluation of molecular markers related to cell cycle and apoptosis (), oxidative stress (), conjugation and detoxification of xenobiotics ( and ), DNA damage ( and ), and SUMOylation processes ( and ) in order to identify any potential alterations in pathways that are normally activated at the cellular level. The results showed that contaminants tend to affect the enzymatic detoxification and antioxidant system, influencing DNA repair defense mechanisms involved in resistance to oxidative stress. The combined effect of the compounds at sub-lethal doses results in a greater activation of these pathways compared to exposure to each compound alone, thereby exacerbating their cytotoxicity. The biomarkers analyzed could contribute to the definition of early warning markers useful for environmental monitoring, while simultaneously providing insight into the toxicity and hazard levels of these substances in the environment and associated health risks.

摘要

随着时间的推移,科学界对不同化合物混合物的影响越来越感兴趣,目前尚无关于某些类别外源性物质的既定证据或知识。众所周知,接触污染物会导致氧化应激,导致活性氧(ROS)的过度产生,这会影响调节细胞周期、细胞凋亡、能量平衡和细胞代谢的信号通路。本研究的目的是调查新兴污染物和药物混合物的亚致死浓度对与毒性、氧化应激和癌症相关的生物标志物调节的影响。在本研究中,将肝癌细胞系HepG2分别暴露于浓度不断增加的多溴二苯醚47(BDE-47)、氯化镉(CdCl)和卡马西平(CBZ)中,单独暴露和混合暴露72小时,以使用MTT试验评估细胞毒性。在确定亚致死浓度后的后续步骤是,通过评估与细胞周期和细胞凋亡相关的分子标志物、氧化应激、外源性物质的结合和解毒、DNA损伤以及SUMO化过程,在基因表达水平上研究暴露的影响,以便确定在细胞水平上正常激活的通路中是否存在任何潜在改变。结果表明,污染物倾向于影响酶解毒和抗氧化系统,影响参与氧化应激抗性的DNA修复防御机制。与单独暴露于每种化合物相比,亚致死剂量的化合物联合作用导致这些通路的更大激活,从而加剧其细胞毒性。所分析的生物标志物有助于定义对环境监测有用的早期预警标志物,同时深入了解这些物质在环境中的毒性和危害水平以及相关的健康风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2114/11509268/de8857acc0b1/metabolites-14-00559-g001.jpg

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