Somatic mutation of the APC gene in thyroid carcinoma associated with familial adenomatous polyposis

被引:25
|
作者
Iwama, T
Konishi, M
Iijima, T
Yoshinaga, K
Tominaga, T
Koike, M
Miyaki, M
机构
[1] Tokyo Metropolitan Komagome Hosp, Hereditary Tumor Res Project, Bunkyo Ku, Tokyo 1138677, Japan
[2] Tokyo Metropolitan Komagome Hosp, Dept Surg, Bunkyo Ku, Tokyo 1138677, Japan
[3] Tokyo Metropolitan Komagome Hosp, Dept Pathol, Bunkyo Ku, Tokyo 1138677, Japan
[4] Kyoundo Hosp, Sasaki Inst, Dept Surg, Chiyoda Ku, Tokyo 1010062, Japan
[5] Tokyo Med & Dent Univ, Dept Surg 2, Bunkyo Ku, Tokyo 1130034, Japan
[6] Showa Univ, Inst Mol Oncol, Shinagawa Ku, Tokyo 1428555, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1999年 / 90卷 / 04期
关键词
familial adenomatous polyposis; thyroid carcinoma; somatic mutation of APC gene; histology of thyroid carcinoma;
D O I
10.1111/j.1349-7006.1999.tb00757.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report the existence of both germline and somatic mutations of the APC gene in thyroid carcinomas from familial adenomatous polyposis (FAP) patients, one papillary thyroid carcinoma from a 20-year-old woman, with germline mutation of the APC gene (TCA to TGA at codon 1110), showed a somatic mutation of AAAAC deletion between codons 1060 and 1063. Another somatic mutation of CAG to TAG at codon 886 was also found in one of multiple thyroid carcinomas from a 26-year-old woman with attenuated FAP and germline mutation at codon 175 (C deletion). This is the first evidence that total absence of the normal function of the APC gene is involved in development of thyroid carcinomas in FAP.
引用
收藏
页码:372 / 376
页数:5
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