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Genetic features of thyroid hormone receptors
Maha Rebaï1, Imen Kallel, Ahmed Rebaï
1Molecular and Cellular Diagnosis Processes, Centre of Biotechnology of Sfax, University of Sfax, Route Sidi Mansour, PO Box 1177, 3018 Sfax, Tunisia.
Abstract:
Thyroid hormone receptors (TR) are prototypes of nuclear transcription factors that regulate the expression of target genes. These receptors play an important role in many physiological processes. Moreover, a dysfunction of these proteins is often implicated in several human diseases and malignancies. Here we report genetic variations and alterations of the TRs that have been described in the literature as well as their potential role in the development of some human diseases including cancers. The functional effects of some mutations and polymorphisms in TRs on disease susceptibility, especially on cancer risk, are now established. Therefore, further investigations are needed in order to use these receptors as therapeutic targets or as biological markers to decide on appropriate forms of treatment.
Insights
Thyroid hormone receptors (TRs) regulate gene expression and are crucial for physiological processes. Genetic variations in TRs are linked to human diseases, including cancer, highlighting their potential as therapeutic targets.
Area of Science:
- Endocrinology
- Molecular Biology
- Genetics
Background:
- Thyroid hormone receptors (TRs) are nuclear transcription factors regulating gene expression.
- TRs are vital for numerous physiological functions.
- TR dysfunction is associated with human diseases and cancers.
Purpose of the Study:
- To review genetic variations and alterations of TRs.
- To explore the role of TRs in disease development, particularly cancers.
- To establish the functional effects of TR mutations and polymorphisms on disease susceptibility.
Main Methods:
- Literature review of genetic variations and alterations in TRs.
- Analysis of the functional effects of TR mutations and polymorphisms.
- Assessment of the association between TRs and cancer risk.
Main Results:
- Genetic variations and alterations in TRs are documented in scientific literature.
- The functional impact of certain TR mutations and polymorphisms on disease susceptibility, especially cancer risk, is established.
- TRs play a significant role in the pathogenesis of various human diseases.
Conclusions:
- TRs are critical regulators of gene expression with implications in human health and disease.
- Genetic alterations in TRs contribute to disease development, including malignancies.
- Further research into TRs is essential for developing novel therapeutic strategies and biomarkers for cancer treatment.
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