Guigon Celine J, Cheng Sheue-yann
Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-4264, USA.
IUBMB Life. 2009 May;61(5):528-36. doi: 10.1002/iub.180.
The thyroid hormone, T3, plays important roles in metabolism, growth, and differentiation. Germline mutations in thyroid hormone receptor beta (TRbeta) have been identified in many individuals with resistance to thyroid hormone, a syndrome of reduced sensitivity to T3. A close association of somatic mutations of TRbeta with several human cancers has become increasingly apparent, but how TRbeta mutants could be involved in the carcinogenesis in vivo has not been addressed. The creation of a mouse model (TRbeta(PV/PV) mouse) that harbors a knockin mutation of TRbeta (denoted TRbetaPV) has facilitated the study of the molecular actions of TRbeta mutants in vivo. The striking phenotype of thyroid cancer and the development of pituitary tumors exhibited by TRbeta(PV/PV) mice have uncovered novel functions of a TRbeta mutant in tumorigenesis. It led to the important findings that the oncogenic action of TRbetaPV is mediated by both genomic and nongenomic actions to alter gene expression and signaling pathways activity.
甲状腺激素T3在新陈代谢、生长和分化过程中发挥着重要作用。许多甲状腺激素抵抗综合征(一种对T3敏感性降低的综合征)患者体内已发现甲状腺激素受体β(TRβ)的种系突变。TRβ的体细胞突变与几种人类癌症之间的密切关联日益明显,但TRβ突变体如何在体内参与致癌过程尚未得到研究。创建一种携带TRβ敲入突变(称为TRβPV)的小鼠模型(TRβ(PV/PV)小鼠)有助于研究TRβ突变体在体内的分子作用。TRβ(PV/PV)小鼠表现出的甲状腺癌显著表型和垂体肿瘤的发生揭示了TRβ突变体在肿瘤发生中的新功能。这导致了重要发现,即TRβPV的致癌作用是通过基因组和非基因组作用介导的,以改变基因表达和信号通路活性。