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六氟环氧丙烷二聚酸(GenX)暴露可诱导肝癌细胞系(HepG2)细胞凋亡。

Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells.

作者信息

Yoo Hee Joon, Pyo Min Cheol, Park Yoonjin, Kim Bo Yong, Lee Kwang-Won

机构信息

Department of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul 02841, Republic of Korea.

Department of Clinical Laboratory Sciences, College of Health Science, Korea University, Seoul 02841, Republic of Korea.

出版信息

Heliyon. 2021 Oct 28;7(11):e08272. doi: 10.1016/j.heliyon.2021.e08272. eCollection 2021 Nov.

Abstract

Hexafluoropropylene oxide dimer acid, also known as GenX, is a poly- and perfluoroalkyl substance (PFAS). PFASs are nonvolatile synthetic substances that can be readily disseminated into the environment during processing and use, making them easy to implement in the soil, drinking water, and air. Compared to other PFASs, GenX has a comparatively short carbon chain length and is expected to have a lower tendency to accumulate in humans; therefore, GenX has recently been used as a substitute to other PFASs. However, the mechanisms underlying GenX action and intoxication in humans remains unclear. In this study, the apoptotic capacity of GenX in human liver cells was investigated. When representative human-derived liver cells (HepG2 cells) were treated with GenX for 12 h, cell viability was reduced, and apoptosis was greatly increased. In addition, GenX increased the generation of intracellular reactive oxygen species (ROS), indicating the induction of oxidative stress in a dose-dependent manner. GenX treatment increased the expression of major apoptosis-related genes relative to the untreated control group. This research indicates that GenX causes apoptosis through ROS mediation in HepG2 cells, which may expand our knowledge of the molecular and toxicological mechanisms of GenX.

摘要

六氟环氧丙烷二聚酸,也称为GenX,是一种多氟和全氟烷基物质(PFAS)。PFAS是不易挥发的合成物质,在加工和使用过程中很容易扩散到环境中,使其易于在土壤、饮用水和空气中存在。与其他PFAS相比,GenX的碳链长度相对较短,预计在人体中积累的倾向较低;因此,GenX最近被用作其他PFAS的替代品。然而,GenX在人体中的作用和中毒机制仍不清楚。在本研究中,研究了GenX在人肝细胞中的凋亡能力。当用GenX处理代表性的人源肝细胞(HepG2细胞)12小时时,细胞活力降低,凋亡显著增加。此外,GenX增加了细胞内活性氧(ROS)的产生,表明以剂量依赖的方式诱导氧化应激。与未处理的对照组相比,GenX处理增加了主要凋亡相关基因的表达。本研究表明,GenX通过ROS介导在HepG2细胞中引起凋亡,这可能会扩展我们对GenX分子和毒理学机制的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/115a/8571496/00ec89f4caf1/ga1.jpg

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