Jabeen Musarrat, Fayyaz Muhammad, Irudayaraj Joseph
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Biomedical Research Centre (BRC) at Mills Breast Cancer Institute, Carle Foundation Hospital, Urbana, IL 61801, USA.
Toxics. 2020 Nov 23;8(4):112. doi: 10.3390/toxics8040112.
Per- and polyfluoroalkyl substances (PFAS) are a group of human-made compounds with strong C-F bonds, and have been used in various manufacturing industries for decades. PFAS have been reported to deleterious effect on human health, which has led to studies identifying the possible toxicity and toxicity routes of these compounds. We report that these compounds have the potential to cause epigenetic modifications, and to induce dysregulation in the cell proliferation cycle as well as apoptosis in A549 lung cancer cells when exposed to 10-, 200- and 400 μM concentrations of each compound. Our studies show that exposure to perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) may cause hypomethylation in the epigenome, but changes in the epigenetic makeup are not evident upon exposure to GenX. We establish that exposure to lower doses of these compounds causes the cells' balance to shift to cell proliferation, whereas exposure to higher concentrations shifts the balance more towards apoptosis. Furthermore, the apoptosis pathway upon exposure to GenX, PFOA, and PFOS has also been identified. Our findings suggest that exposure to any of these compounds may have profound effects in patients with pre-existing lung conditions or could trigger lung cancinogenesis.
全氟和多氟烷基物质(PFAS)是一类具有强碳氟键的人造化合物,已在各种制造业中使用了数十年。据报道,PFAS对人类健康有有害影响,这促使人们开展研究以确定这些化合物可能的毒性及毒性途径。我们报告称,当A549肺癌细胞暴露于每种化合物的10μM、200μM和400μM浓度时,这些化合物有可能导致表观遗传修饰,并诱导细胞增殖周期失调以及细胞凋亡。我们的研究表明,暴露于全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)可能会导致表观基因组发生低甲基化,但暴露于GenX后表观遗传组成的变化并不明显。我们确定,暴露于较低剂量的这些化合物会使细胞平衡转向细胞增殖,而暴露于较高浓度则会使平衡更多地转向细胞凋亡。此外,还确定了暴露于GenX、PFOA和PFOS后的细胞凋亡途径。我们的研究结果表明,暴露于这些化合物中的任何一种都可能对已有肺部疾病的患者产生深远影响,或引发肺癌。