Poghosyan Zaruhi, Wynford-Thomas David
Department of Pathology, School of Medicine, Cardiff University, Cardiff, Wales, United Kingdom.
Methods Enzymol. 2006;407:648-60. doi: 10.1016/S0076-6879(05)07051-5.
Activation of Ras oncogene by point mutations is an early frequent event in thyroid tumorigenesis. In this chapter, we describe the use of human primary thyroid follicular epithelial cells expressing oncogenic mutant Ras by means of retroviral transduction as a biological model of human cancer initiation that provides powerful insights into thyroid tumorigenesis. We describe protocols for manipulating primary epithelial cells and describe the use of this model to dissect the signaling pathways required for Ras-induced proliferation in these cells. We also highlight the importance of studying Ras signaling in an appropriate cell context, summarizing some of the key differences identified between more widespread experimental models based on fibroblasts or rodent cell lines and primary epithelial cells.
通过点突变激活Ras癌基因是甲状腺肿瘤发生过程中早期常见的事件。在本章中,我们描述了通过逆转录病毒转导使用表达致癌突变型Ras的人原发性甲状腺滤泡上皮细胞作为人类癌症起始的生物学模型,该模型为甲状腺肿瘤发生提供了有力的见解。我们描述了操纵原代表皮细胞的方案,并描述了使用该模型剖析这些细胞中Ras诱导增殖所需的信号通路。我们还强调了在适当的细胞环境中研究Ras信号传导的重要性,总结了基于成纤维细胞或啮齿动物细胞系的更广泛实验模型与原代表皮细胞之间发现的一些关键差异。