Literature DB >> 11128715

A Phe 486 thyrotropin receptor mutation in an autonomously functioning follicular carcinoma that was causing hyperthyroidism.

P Camacho1, D Gordon, E Chiefari, S Yong, S DeJong, S Pitale, D Russo, S Filetti.   

Abstract

Hot nodules are rarely found to be carcinomas. We report a case of a nonmetastatic follicular carcinoma that presented as a hot nodule that was causing hyperthyroidism. A base substitution (ATC for TTC) was found in codon 486 of the TSH receptor gene and this resulted in the substitution of an isoleucine for a phenylalanine in the first extracellular loop of the receptor. This was absent in the deoxyribonucleic acid from the surrounding normal thyroid tissue indicating its somatic origin. This mutation, which was previously reported to activate both cyclic adenosine monophosphate and the inositol phosphate-diacylglycerol cascades, may have been responsible for the constitutive activation of the thyrotropin receptor and resulting hyperfunction of this follicular carcinoma.

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Year:  2000        PMID: 11128715     DOI: 10.1089/thy.2000.10.1009

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  13 in total

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Journal:  Eur J Pediatr       Date:  2008-01-04       Impact factor: 3.183

8.  Thyroid Stimulating Hormone Receptor.

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9.  Clinical Significance of Thyroid-Stimulating Hormone Receptor Gene Mutations and/or Sodium-Iodine Symporter Gene Overexpression in Indeterminate Thyroid Fine Needle Biopsies.

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10.  A solitary hyperfunctioning thyroid nodule harboring thyroid carcinoma: review of the literature.

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