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Updated: Aug 12, 2026

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
Human malignant thyroid tumors displayed reduced levels of transforming growth factor beta receptor type II messenger
D Lazzereschi1, A Ranieri, G Mincione
1Dipartimento di Medicina Sperimentale, Università La Sapienza, Rome, Italy.
Abstract:
Transforming growth factor beta (TGF-beta) is a physiological regulator of thyroid epithelial cell growth and differentiation. This factor signals through a heteromeric complex composed of type I (TGF-beta receptor type I) and type II [TGF-beta receptor type II (TbetaRII)] receptors. Loss of TbetaRII expression has been related to resistance to TGF-beta inhibition of cell proliferation. In the present work, we analyzed the TbetaRII expression in a series of human thyroid tumors, from benign lesions (adenomas) to neoplastic lesions of increasing aggressiveness (papillary and follicular carcinomas) up to the extremely aggressive anaplastic tumors. Results obtained indicated a clear reduced expression of TbetaRII mRNA only in the group of thyroid carcinomas when compared with their relative normal tissues. Immunohistochemical analyses with specific anti-TbetaRII antibodies confirm these observations. These data indicate that loss of expression of TbetaRII can contribute to thyroid cancer progression, inducing cancer cells to escape the growth-inhibitory effect of TGF-beta.
Insights
Transforming growth factor beta receptor type II (TbetaRII) expression is reduced in thyroid carcinomas. This loss of TbetaRII may drive thyroid cancer progression by enabling cells to evade TGF-beta growth inhibition.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Transforming growth factor beta (TGF-beta) regulates thyroid epithelial cell growth and differentiation.
- TGF-beta signaling involves a receptor complex including TGF-beta receptor type II (TbetaRII).
- Reduced TbetaRII expression is linked to resistance to TGF-beta's anti-proliferative effects.
Purpose of the Study:
- To investigate TbetaRII expression in various human thyroid tumors.
- To determine the correlation between TbetaRII expression levels and thyroid tumor aggressiveness.
- To elucidate the role of TbetaRII loss in thyroid cancer progression.
Main Methods:
- Analysis of TbetaRII messenger RNA (mRNA) expression in thyroid tissues.
- Immunohistochemical analysis using specific anti-TbetaRII antibodies.
- Comparison of TbetaRII expression in benign lesions, carcinomas, and anaplastic tumors versus normal thyroid tissue.
Main Results:
- Significantly reduced TbetaRII mRNA expression was observed specifically in thyroid carcinomas compared to normal thyroid tissues.
- Immunohistochemical analyses corroborated the reduced expression of TbetaRII.
- TbetaRII expression levels correlated with tumor aggressiveness, being lowest in advanced carcinomas.
Conclusions:
- Loss of TbetaRII expression is a feature of thyroid carcinomas.
- Reduced TbetaRII contributes to thyroid cancer progression by impairing TGF-beta-mediated growth inhibition.
- Targeting TbetaRII pathways could be a strategy for thyroid cancer treatment.
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