Low frequency of BRAFT1796A mutations in childhood thyroid carcinomas

被引:115
作者
Kumagai, A
Namba, H
Saenko, VA
Ashizawa, K
Ohtsuru, A
Ito, M
Ishikawa, N
Sugino, K
Ito, K
Jeremiah, S
Thomas, GA
Bogdanova, TI
Tronko, MD
Nagayasu, T
Shibata, Y
Yamashita, S
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Atom Bomb Dis Inst, Dept Mol Med, Nagasaki 8528523, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Atom Bomb Dis Inst, Dept Radiat Epidemiol, Nagasaki 8528523, Japan
[3] Nagasaki Univ Hosp, Dept Surg, Nagasaki 8528523, Japan
[4] Nagasaki Univ Hosp, Takashi Nagai Mem Int Hibakusha Med Ctr, Nagasaki 8528523, Japan
[5] Natl Nagasaki Med Ctr, Dept Pathol, Omura 8568562, Japan
[6] Ito Hosp, Tokyo 1508308, Japan
[7] Singleton Hosp, S W Wales Canc Inst, Swansea SA2 8QA, W Glam, Wales
[8] Ukraine Acad Med Sci, Inst Endocrinol & Metab, Lab Morphol Endocrine Syst, UA-04114 Kiev, Ukraine
关键词
D O I
10.1210/jc.2004-0172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A high prevalence of the activating BRAF mutation, BRAF(T1796A), is observed in adult papillary thyroid carcinomas (PTCs). The prognosis of childhood PTCs is generally fairly good despite the fact that distant metastases are often documented in these cases. To investigate the differences between the characteristics of childhood and adult PTCs, we analyzed both BRAF(T1796A) and RAS mutations in 31 Japanese and 48 post-Chernobyl Ukrainian thyroid carcinomas. In the 31 Japanese childhood cases, BRAF(T1796A) was found in only one instance (3.2%), and no RAS mutations were detected. In the Ukrainian subjects, of the 15 childhood and the 33 adolescent and young adult PTCs examined, the BRAF(T1796A) mutation was found in zero and eight cases, respectively, and RAS mutations were found in two of the young adult cases. In addition, 17 of the 48 Ukrainian cases showed expression of the RET tyrosine kinase region, indicating the existence of RET/PTC rearrangements. Unlike adult PTCs, we could detect no positive association between BRAF(T1796A) mutations and clinical parameters in the childhood carcinomas, suggesting that a low prevalence of BRAF(T1796A) is a common feature of PTCs in children regardless of radiation exposure levels. The differences in the prevalence of BRAF(T1796A) mutations between childhood and adult cases of PTC may well reflect inherent differences in the clinical features of these cancers between the two age groups.
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页码:4280 / 4284
页数:5
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