Mechanistic Toxicology Branch, Division of Translational Toxicology, National Institute of Environmental Health Sciences (NIEHS), 111 TW Alexander Drive, Research Triangle Park, NC 27709, USA.
Mechanistic Toxicology Branch, Division of Translational Toxicology, National Institute of Environmental Health Sciences (NIEHS), 111 TW Alexander Drive, Research Triangle Park, NC 27709, USA.
Toxicol In Vitro. 2023 Jun;89:105577. doi: 10.1016/j.tiv.2023.105577. Epub 2023 Feb 26.
Perfluorooctanoic acid (PFOA) is tumorigenic in rats and mice and potentially tumorigenic in humans. Here, we studied long-term PFOA exposure with an in vitro transformation model using the rat liver epithelial cell, TRL 1215. Cells were cultured in 10 μM (T10), 50 μM (T50) and 100 μM (T100) PFOA for 38 weeks and compared to passage-matched control cells. T100 cells showed morphological changes, loss of cell contact inhibition, formation of multinucleated giant and spindle-shaped cells. T10, T50, and T100 cells showed increased LC values 20%, 29% to 35% above control with acute PFOA treatment, indicating a resistance to PFOA toxicity. PFOA-treated cells showed increases in Matrix metalloproteinase-9 secretion, cell migration, and developed more and larger colonies in soft agar. Microarray data showed Myc pathway activation at T50 and T100, associating Myc upregulation with PFOA-induced morphological transformation. Western blot confirmed that PFOA produced significant increases in c-MYC protein expression in a time- and concentration-related manner. Tumor invasion indicators MMP-2 and MMP-9, cell cycle regulator cyclin D1, and oxidative stress protein GST were all significantly overexpressed in T100 cells. Taken together, chronic in vitro PFOA exposure produced multiple cell characteristics of malignant progression and differential gene expression changes suggestive of rat liver cell transformation.
全氟辛酸(PFOA)在大鼠和小鼠中具有致癌性,在人类中也具有潜在的致癌性。在这里,我们使用大鼠肝上皮细胞 TRL 1215 研究了体外转化模型中的长期 PFOA 暴露。细胞分别在 10 μM(T10)、50 μM(T50)和 100 μM(T100)PFOA 中培养 38 周,并与传代匹配的对照细胞进行比较。T100 细胞表现出形态变化、失去细胞接触抑制、形成多核巨细胞和纺锤形细胞。T10、T50 和 T100 细胞在急性 PFOA 处理后,LC 值分别比对照增加了 20%、29%至 35%,表明对 PFOA 毒性具有抗性。PFOA 处理的细胞表现出基质金属蛋白酶-9 分泌增加、细胞迁移增加,并在软琼脂中形成更多和更大的集落。微阵列数据显示 T50 和 T100 中 Myc 通路的激活,与 Myc 上调与 PFOA 诱导的形态转化相关。Western blot 证实 PFOA 以时间和浓度相关的方式显著增加 c-MYC 蛋白的表达。肿瘤侵袭指标 MMP-2 和 MMP-9、细胞周期调节剂 cyclin D1 和氧化应激蛋白 GST 在 T100 细胞中均过度表达。综上所述,慢性体外 PFOA 暴露产生了多个恶性进展的细胞特征和差异基因表达变化,提示大鼠肝细胞转化。