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首页> 外文期刊>Environmental Science: Nano >Acquisition of cancer stem cell-like properties in human small airway epithelial cells after a long-term exposure to carbon nanomaterials
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Acquisition of cancer stem cell-like properties in human small airway epithelial cells after a long-term exposure to carbon nanomaterials

机译:在长期暴露于碳纳米材料后,在人小气道上皮细胞中获取癌症干细胞样特性

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Cancer stem cells (CSCs) are a key driver of tumor formation and metastasis, but how they are affected by nanomaterials is largely unknown. The present study investigated the effects of different carbon-based nanomaterials (CNMs) on neoplastic and CSC-like transformation of human small airway epithelial cells and determined the underlying mechanisms. Using a physiologically relevant exposure model (long-term/low-dose) with system validation using a human carcinogen, asbestos, we demonstrated that single-walled carbon nanotubes, multi-walled carbon nanotubes, ultrafine carbon black, and crocidolite asbestos induced particle-specific anchorage-independent colony formation, DNA-strand breaks, and p53 downregulation, indicating the genotoxicity and carcinogenic potential of CNMs. The chronic CNM-exposed cells exhibited CSC-like properties as indicated by 3D spheroid formation, anoikis resistance, and CSC marker expression. Mechanistic studies revealed specific self-renewal and epithelial-mesenchymal transition (EMT)-related transcription factors that are involved in the cellular transformation process. Pathway analysis of gene signaling networks supports the role of SOX2 and SNAI1 signaling in CNM-mediated transformation. These findings support the potential carcinogenicity of high aspect ratio CNMs and identified molecular targets and signaling pathways that may contribute to disease development.
机译:癌症干细胞(CSCs)是肿瘤形成和转移的关键驱动器,但它们如何受纳米材料的影响在很大程度上。本研究研究了不同碳基纳米材料(CNMS)对人小气道上皮细胞的肿瘤和CSC样变性的影响,并确定了潜在机制。使用生理学相关的曝光模型(长期/低剂量)使用使用人类致癌的系统验证,我们证明了单壁碳纳米管,多壁碳纳米管,超细炭黑和鳄鱼石棉诱导的粒子 - 特定的锚固无关的菌落形成,DNA-链断裂和P53下调,表明CNMS的遗传毒性和致癌潜力。慢性CNM暴露的细胞表现出CSC样性质,如3D球形形成,Anoikis抗性和CSC标记表达所示。机械研究揭示了涉及细胞转化过程的特异性自我更新和上皮 - 间充质转换(EMT)相关的转录因子。基因信号通信网络的途径分析支持SOX2和SNAI1信号传导在CNM介导的转化中的作用。这些发现支持高纵横比CNMS的潜在致癌性,并确定可能有助于疾病发展的分子靶标和信号通路。

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