Different genotype distribution of the GNB3 C825T polymorphism of the G protein β3 subunit in adenomas and differentiated thyroid carcinomas of follicular cell origin

• Published in: The Journal of pathology 2005-12, Vol.207 (4), p.430-435
• Main Authors: Sheu, Sien-Yi, Görges, Rainer, Ensinger, Christian, Öfner, Dietmar, Farid, Nadir R, Siffert, Winfried, Schmid, Kurt Werner
• Format: Article
• Language: English
• Subjects: allele frequency; Biological and medical sciences; Endocrinopathies; G protein; genotyping; GNB3; Investigative techniques, diagnostic techniques (general aspects); Malignant tumors; Medical sciences; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; polymorphism; signal transduction; thyroid cancer; Thyroid. Thyroid axis (diseases)
• ISSN: 0022-3417; 1096-9896
• DOI: 10.1002/path.1857

A C825T polymorphism has been demonstrated in the GNB3 gene that encodes the Gβ3 subunit of heterotrimeric G proteins. Due to enhanced G protein activation, the GNB3 825T allele is associated with an increased signal transduction activity. To elucidate a possible role in the development and course of thyroid tumours of follicular cell origin, C825T polymorphism genotypes and allele frequencies were investigated in a series of adenomas and differentiated carcinomas. Genotypes and the allele frequency of the Gβ3 polymorphism were investigated in samples from 361 patients (all white Caucasians) with differentiated thyroid tumours of follicular cell origin [80 adenomas and 95 follicular (FTCs) and 186 papillary carcinomas (PTCs)]. The results were compared with those of 1859 healthy controls. Both the genotype distribution (p = 0.029) and the allele frequency (p = 0.028) of the adenoma group were statistically significantly different from those of the control group. Thyroid adenomas also differed for both parameters significantly from FTCs (p = 0.042 and 0.033, respectively) and PTCs (0.0018 and 0.0081, respectively), whereas no statistical difference was noted between the FTC and PTC groups. Although the biological significance of these observations remains obscure, the results are suggestive of a putative role for the GNB3 polymorphism in thyroid tumour development and/or progression. Further research has to elucidate if, and to what extent, this common germ‐line variation influences the TSH‐triggered signalling pathways responsible for thyroid function and proliferation. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.