Zhu Xuguang, Cheng Sheue-Yann
Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Methods Mol Biol. 2018;1801:207-223. doi: 10.1007/978-1-4939-7902-8_17.
Analysis of thyroid tumorigenesis in xenograft mouse model is important to study human thyroid cancer. Recent studies have made big strides toward understanding the molecular mechanisms by which thyroid hormone nuclear receptors (TR) act to maintain normal cellular functions in growth, differentiation, and development. Despite growing interest, the role of TR in oncogenesis remains to be fully elucidated. Two TR genes give rise to three major TR isoforms: TRα1, TRβ1, and TRβ2. These TR subtypes express in a tissue- and development-dependent manner. Research has been directed at understanding the mechanisms by which TR could mediate aberrant cellular signaling that contributes to oncogenesis, at dissecting possible distinct roles of TR isoforms in oncogenesis, and at the differential susceptibility of target tissues to the oncogenic actions of TR. This chapter gives a brief overview of the current undersatanding of known molecular oncogenic actions of TR. Here, we describe analysis of thyroid tumorigenesis used in interrogating the in vivo oncogenic actions of TR.
在异种移植小鼠模型中分析甲状腺肿瘤发生对于研究人类甲状腺癌很重要。最近的研究在理解甲状腺激素核受体(TR)维持生长、分化和发育过程中正常细胞功能的分子机制方面取得了重大进展。尽管人们对此兴趣日益浓厚,但TR在肿瘤发生中的作用仍有待充分阐明。两个TR基因产生三种主要的TR亚型:TRα1、TRβ1和TRβ2。这些TR亚型以组织和发育依赖性方式表达。研究方向包括了解TR介导导致肿瘤发生的异常细胞信号传导的机制,剖析TR亚型在肿瘤发生中可能的不同作用,以及靶组织对TR致癌作用的不同易感性。本章简要概述了目前对TR已知分子致癌作用的理解。在此,我们描述了用于探究TR体内致癌作用的甲状腺肿瘤发生分析。