日本放射線影響学会大会講演要旨集
The 47th Annual Meeting of The Japan Radiation Research Society
セッションID: 3M-11
会議情報

Oncogenesis
The BRAFT1796A mutation associates with patents age but not with radiation ethiology of human papillary thyroid cancer
*Vladimir SaenkoTatiana RogounovitchHiroyuki NambaIlya SedliarouAtsushi KumagaiAlexandr AbrosimovEvgenii LushnikovPavel RoumiantsevTatiana BogdanovaMykola TronkoShunichi Yamashita
著者情報
会議録・要旨集 フリー

詳細
抄録
BRAFT1796A transversion has been shown to be a prevalent event in human papillary thyroid carcinomas (PTCs). In this study the mutation prevalence was examined in radiation-associated PTCs. DNA from the post-Chernobyl (age at exposure below 18 years old) and sporadic PTCs was analyzed by direct sequencing and mutation allele-specific PCR. In the whole radiation-associated PTC group, BRAFT1796A was found in 17/98 (17.3%) cases with no overall statistical difference from sporadic cases (14/53, 26.4%). However, when radiation-associated series was subdivided in the pediatric (age below 18 years old at diagnosis) and adult cases (age over 18 years old at diagnosis), it was found that in the younger patients the mutational frequency was significantly lower than that in the elder ones, 4/49 (8.2%) versus 13/49 (26.5%), p=0.03. Thus, the BRAFT1796A mutational rate in PTCs does not associate with radiation history of patients but rather increases with individuals age.
著者関連情報
© 2004 The Japan Radiation Research Society
前の記事 次の記事
feedback
Top