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

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. Co...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Hee Joon Yoo, Min Cheol Pyo, Yoonjin Park, Bo Yong Kim, Kwang-Won Lee
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://doaj.org/article/42880c08c6894e9b8c459a40d9444d98
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:42880c08c6894e9b8c459a40d9444d98
record_format dspace
spelling oai:doaj.org-article:42880c08c6894e9b8c459a40d9444d982021-12-02T05:02:22ZHexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells2405-844010.1016/j.heliyon.2021.e08272https://doaj.org/article/42880c08c6894e9b8c459a40d9444d982021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2405844021023756https://doaj.org/toc/2405-8440Hexafluoropropylene 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.Hee Joon YooMin Cheol PyoYoonjin ParkBo Yong KimKwang-Won LeeElsevierarticlePoly- and perfluoroalkyl substanceHexafluoropropylene oxide dimer acidOxidative stressApoptosisLiver cellsScience (General)Q1-390Social sciences (General)H1-99ENHeliyon, Vol 7, Iss 11, Pp e08272- (2021)
institution DOAJ
collection DOAJ
language EN
topic Poly- and perfluoroalkyl substance
Hexafluoropropylene oxide dimer acid
Oxidative stress
Apoptosis
Liver cells
Science (General)
Q1-390
Social sciences (General)
H1-99
spellingShingle Poly- and perfluoroalkyl substance
Hexafluoropropylene oxide dimer acid
Oxidative stress
Apoptosis
Liver cells
Science (General)
Q1-390
Social sciences (General)
H1-99
Hee Joon Yoo
Min Cheol Pyo
Yoonjin Park
Bo Yong Kim
Kwang-Won Lee
Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
description 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.
format article
author Hee Joon Yoo
Min Cheol Pyo
Yoonjin Park
Bo Yong Kim
Kwang-Won Lee
author_facet Hee Joon Yoo
Min Cheol Pyo
Yoonjin Park
Bo Yong Kim
Kwang-Won Lee
author_sort Hee Joon Yoo
title Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
title_short Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
title_full Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
title_fullStr Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
title_full_unstemmed Hexafluoropropylene oxide dimer acid (GenX) exposure induces apoptosis in HepG2 cells
title_sort hexafluoropropylene oxide dimer acid (genx) exposure induces apoptosis in hepg2 cells
publisher Elsevier
publishDate 2021
url https://doaj.org/article/42880c08c6894e9b8c459a40d9444d98
work_keys_str_mv AT heejoonyoo hexafluoropropyleneoxidedimeracidgenxexposureinducesapoptosisinhepg2cells
AT mincheolpyo hexafluoropropyleneoxidedimeracidgenxexposureinducesapoptosisinhepg2cells
AT yoonjinpark hexafluoropropyleneoxidedimeracidgenxexposureinducesapoptosisinhepg2cells
AT boyongkim hexafluoropropyleneoxidedimeracidgenxexposureinducesapoptosisinhepg2cells
AT kwangwonlee hexafluoropropyleneoxidedimeracidgenxexposureinducesapoptosisinhepg2cells
_version_ 1718400763975172096