Metastatic Follicular Thyroid Carcinoma Arising from Congenital Goiter as a Result of a Novel Splice Donor Site Mutation in the Thyroglobulin Gene

• Published in: The journal of clinical endocrinology and metabolism Vol. 91; no. 3; pp. 740 - 746
• Main Authors: Alzahrani, Ali S, Baitei, Essa Y, Zou, Minjing, Shi, Yufei
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Endocrine Society 01.03.2006
• Subjects: Biological and medical sciences; Endocrinopathies; Fundamental and applied biological sciences. Psychology; Malignant tumors; Medical sciences; Thyroid. Thyroid axis (diseases); Vertebrates: endocrinology; Endocrinopathy; Congenital; Splicing; Donor site; Thyroid diseases; Malignant tumor; Metastasis; Follicular carcinoma; Thyroid carcinoma; Thyroid cancer; Gene; Thyroglobulin; Goiter; Thyroid hormone; Genetics; Advanced stage; Mutation; Endocrinology
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2005-2302

Context: Defects in thyroglobulin (Tg) synthesis are one of the causes of thyroid dyshormonogenesis. Only a few mutations in the Tg gene have been described. Objectives: We describe a novel Tg gene mutation and discuss the mechanisms by which it causes dyshormonogenesis with subsequent malignant transformation. Cases: Two siblings aged 21 and 19 yr presented with recurrent goiters for which they had undergone multiple thyroid surgeries since early childhood. The older sibling was diagnosed with metastatic follicular thyroid carcinoma at age 15 yr. Methods: The entire coding region and intron-exon boundaries of the Tg gene were amplified and sequenced from the patients. We also sequenced the boundaries of exon 5 and intron 5 from both parents. RT-PCR amplification of a cDNA fragment encompassing exons 4–6 was also performed. Results: A homozygous G to A point mutation at position +1 of the splice donor site of intron 5 (g.IVS5+1G→A) was detected in both patients, whereas a monoallelic mutation was found in their parents. RT-PCR amplification of a cDNA fragment covering exons 4–6 revealed a 191-bp fragment in the patients and 351- and 191-bp fragments in the parents. Sequence analysis of these two fragments confirmed deletion of exon 5 in the 191-bp fragment. Conclusions: Aberrant splicing occurred as a result of the g.IVS5+1G→A mutation, which caused fusion of exons 4 and 6, resulting in the frame shift at codon position 141 and a premature stop codon at position 147 (FS141→147X). The malignant transformation is likely a result of prolonged TSH stimulation.