» Articles » PMID: 22507269

Thyroid Hormone Receptors and Cancer

Overview
Specialties Biochemistry
Biophysics
Date 2012 Apr 18
PMID 22507269
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Thyroid hormone receptors (TRs) are ligand-dependent transcription factors that mediate the actions of the thyroid hormone (T3) in development, growth, and differentiation. The THRA and THRB genes encode several TR isoforms that express in a tissue- and development-dependent manner. In the past decades, a significant advance has been made in the understanding of TR actions in maintaining normal cellular functions. However, the roles of TRs in human cancer are less well understood. The reduced expression of TRs because of hypermethylation, or deletion of TR genes found in human cancers suggests that TRs could function as tumor suppressors. A close association of somatic mutations of TRs with human cancers further supports the notion that the loss of normal functions of TR could lead to uncontrolled growth and loss of cell differentiation.

Scope Of Review: In line with the findings from association studies in human cancers, mice deficient in total functional TRs (Thra1(-/-)Thrb(-/-) mice) or with a targeted homozygous mutation of the Thrb gene (denoted PV; Thrb(PV/PV) mice) spontaneously develop metastatic thyroid carcinoma. This review will examine the evidence learned from these genetically engineered mice that provided strong evidence to support the critical role of TRs in human cancer.

Major Conclusions: Loss of normal functions of TR by deletion or by mutations could contribute to cancer development, progression and metastasis.

General Significance: Novel mechanistic insights are revealed in how aberrant TR activities lead to carcinogenesis. Mouse models of thyroid cancer provide opportunities to identify molecular targets as potential treatment modalities. This article is part of a Special Issue entitled Thyroid hormone signalling.

Citing Articles

The thyroid hormone activating enzyme, DIO2, is a potential pan-cancer biomarker and immunotherapy target.

Nappi A, Miro C, Cicatiello A, Sagliocchi S, Acampora L, Restolfer F J Endocrinol Invest. 2025; .

PMID: 39821172 DOI: 10.1007/s40618-024-02526-9.


Targeting Androgen, Thyroid Hormone, and Vitamin A and D Receptors to Treat Prostate Cancer.

Hantusch B, Kenner L, Stanulovic V, Hoogenkamp M, Brown G Int J Mol Sci. 2024; 25(17).

PMID: 39273194 PMC: 11394715. DOI: 10.3390/ijms25179245.


Transcription factor STAT4 counteracts radiotherapy resistance in breast carcinoma cells by activating the MALAT1/miR-21-5p/THRB regulatory network.

Guo L, Ding G, Ba Y, Tan B, Tian L, Wang K Am J Cancer Res. 2024; 14(4):1501-1522.

PMID: 38726265 PMC: 11076251. DOI: 10.62347/VSJU7227.


Tyrosine kinase inhibitor-induced hypothyroidism: mechanism and clinical implications.

Wang Z, Wang H, Bu C, Meng B, Mu Y, Gao S Eur J Clin Pharmacol. 2024; 80(6):827-838.

PMID: 38483545 DOI: 10.1007/s00228-024-03626-4.


Exploring the Relationship between -MS2 Variants and Susceptibility to Bladder Cancer.

Jeong M, Mun J, Yang G, Kim M, Lee S, Choi Y Genes (Basel). 2024; 15(1).

PMID: 38254939 PMC: 10815179. DOI: 10.3390/genes15010050.


References
1.
Iwasaki Y, Sunaga N, Tomizawa Y, Imai H, Iijima H, Yanagitani N . Epigenetic inactivation of the thyroid hormone receptor beta1 gene at 3p24.2 in lung cancer. Ann Surg Oncol. 2010; 17(8):2222-8. DOI: 10.1245/s10434-010-0956-9. View

2.
Kim W, Guigon C, Fozzatti L, Park J, Lu C, Willingham M . SKI-606, an Src inhibitor, reduces tumor growth, invasion, and distant metastasis in a mouse model of thyroid cancer. Clin Cancer Res. 2012; 18(5):1281-90. PMC: 3294177. DOI: 10.1158/1078-0432.CCR-11-2892. View

3.
Ying H, Furuya F, Zhao L, Araki O, West B, Hanover J . Aberrant accumulation of PTTG1 induced by a mutated thyroid hormone beta receptor inhibits mitotic progression. J Clin Invest. 2006; 116(11):2972-84. PMC: 1592548. DOI: 10.1172/JCI28598. View

4.
Liu J, Stevens J, Rote C, Yost H, Hu Y, Neufeld K . Siah-1 mediates a novel beta-catenin degradation pathway linking p53 to the adenomatous polyposis coli protein. Mol Cell. 2001; 7(5):927-36. DOI: 10.1016/s1097-2765(01)00241-6. View

5.
Yu R, Lu W, Chen J, McCabe C, Melmed S . Overexpressed pituitary tumor-transforming gene causes aneuploidy in live human cells. Endocrinology. 2003; 144(11):4991-8. DOI: 10.1210/en.2003-0305. View