Low Frequency of BRAFT1796A Mutations in Childhood Thyroid Carcinomas

A Kumagai, H Namba, VA Saenko… - The Journal of …, 2004 - academic.oup.com
A Kumagai, H Namba, VA Saenko, K Ashizawa, A Ohtsuru, M Ito, N Ishikawa, K Sugino, K Ito…
The Journal of Clinical Endocrinology & Metabolism, 2004academic.oup.com
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 …
A high prevalence of the activating BRAF mutation, BRAFT1796A, 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 BRAFT1796A and RAS mutations in 31 Japanese and 48 post-Chernobyl Ukrainian thyroid carcinomas. In the 31 Japanese childhood cases, BRAFT1796A 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 BRAFT1796A 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 BRAFT1796A mutations and clinical parameters in the childhood carcinomas, suggesting that a low prevalence of BRAFT1796A is a common feature of PTCs in children regardless of radiation exposure levels. The differences in the prevalence of BRAFT1796A 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.
Oxford University Press