Lin Zhi, Li Yvmo, Zhao Jiarui, Li Jun, Pan Shuang, Wang Xinhe, Lin He, Lin Zhe
College of Pharmacy, Changchun University of Chinese Medicine, China.
Heliyon. 2024 Aug 28;10(17):e37003. doi: 10.1016/j.heliyon.2024.e37003. eCollection 2024 Sep 15.
The objective of this study was to investigate the potential carcinogenic toxicity and mechanisms of PFAS in thyroid, renal, and testicular cancers base on network toxicology and molecular docking techniques. Structural modeling was performed to predict relevant toxicity information, and compounds and cancer-related targets were screened in multiple databases. The interaction of PFAS with three cancers and their key protein targets were explored by combining protein network analysis, enrichment analysis and molecular docking techniques. PFOA, PFOS, and PFHXS exhibited significant carcinogenic and cytotoxic effects. These compounds may induce cancer by mediating active oxygen metabolism and the transduction of phosphatidylinositol 3-kinase/protein kinase B signaling pathway through genes such as ALB, mTOR, MDM2, and ERBB2. Furthermore, the underlying toxic mechanisms may be linked to the pathways in cancer, chemical carcinogenesis through reactive oxygen species/receptor activation, and the FoxO signaling pathway. The results contribute to a comprehensive understanding of the effects of these environmental pollutants on genes, proteins, and metabolic pathways in living organisms. It revealed their toxicity mechanisms in inducing thyroid, renal, and testicular cancers, and provided a solid theoretical foundation for designing new environmental control strategies and drug screening initiatives. Additionally, the integrated application of network toxicology and molecular docking technology can enhance our understanding of the toxicity and mechanisms of unknown environmental pollutants, which is beneficial for protecting the environment and human health.
本研究的目的是基于网络毒理学和分子对接技术,研究全氟烷基和多氟烷基物质(PFAS)在甲状腺癌、肾癌和睾丸癌中的潜在致癌毒性及其机制。进行结构建模以预测相关毒性信息,并在多个数据库中筛选化合物和癌症相关靶点。通过结合蛋白质网络分析、富集分析和分子对接技术,探索PFAS与三种癌症及其关键蛋白质靶点的相互作用。全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)和全氟己基磺酸(PFHXS)表现出显著的致癌和细胞毒性作用。这些化合物可能通过介导活性氧代谢以及通过如白蛋白(ALB)、哺乳动物雷帕霉素靶蛋白(mTOR)、小鼠双微体2(MDM2)和表皮生长因子受体2(ERBB2)等基因的磷脂酰肌醇3激酶/蛋白激酶B信号通路的转导来诱导癌症。此外,潜在的毒性机制可能与癌症中的通路、通过活性氧/受体激活的化学致癌作用以及叉头框蛋白O(FoxO)信号通路有关。这些结果有助于全面了解这些环境污染物对生物体中基因、蛋白质和代谢途径的影响。它揭示了它们在诱导甲状腺癌、肾癌和睾丸癌中的毒性机制,并为设计新的环境控制策略和药物筛选方案提供了坚实的理论基础。此外,网络毒理学和分子对接技术的综合应用可以增强我们对未知环境污染物毒性及其机制的理解,这有利于保护环境和人类健康。