甲状腺癌
医学
癌变
甲状腺癌
癌症研究
端粒酶
突变
V600E型
端粒酶逆转录酶
甲状腺
内科学
肿瘤科
癌症
生物
基因
遗传学
作者
Denise Engelbrecht Zantut‐Wittmann,A.C. Laus,Daniel Antunes Moreno,I.S. Barreto,C.A. Moma,F.F.R. Maia,E.C.S.C. Etchebehere,L.V.M. Assumpção,Rui Manuel Reis
标识
DOI:10.1016/j.amjms.2023.03.019
摘要
BRAF and TERT oncogenes hotspot mutations are associated with a more aggressive outcome in thyroid carcinomas (TC). TERT promoter (pTERT) mutations (C228T and C250T) are related to cancer growth and reduced overall- and disease-free survivals in TC. We report a patient followed up for 8 years with a poorly differentiated thyroid carcinoma (PDTC) presenting an extremely aggressive course, who developed a large volume of metastases in a short period. Molecular analysis of the primary tumor revealed two pTERT mutations (C228T and C250T), and no BRAF V600E mutation. pTERT mutations C228T and C250T have been described as mutually exclusive, indicating that one mutation is enough for telomerase activation and exerts its action in thyroid tumorigenesis. This report describes both pTERT hotspot mutations in the same PDTC patient presenting a very aggressive course, even for PDTC, suggesting a relationship between the two events. However, more studies are needed to prove this causality.
科研通智能强力驱动
Strongly Powered by AbleSci AI