Yang Y
Zhonghua Yi Xue Za Zhi. 1991 Jun;71(6):304-6, 22.
The structure and expression of c-myc oncogene was analyzed by molecular hybridization in tumor tissues from 15 patients with primary thyroid carcinoma, 3 patients with thyroid adenoma and in tissues from 5 normal and 1 adjacent non-neoplastic thyroid. We found that in 9 of the 15 cancer patients, c-myc oncogene was overexpressed (ie, at levels 3-11 times higher than in normal thyroid tissues). Rearrangement of c-myc gene was observed in 4 cancer samples, of which one showed a 150-fold amplification of c-myc gene. Overexpression, amplification of c-myc gene were frequently detected in thyroid cancer patients with more malignant and unfavourable prognosis, which suggested that overexpression, amplification and rearrangement of c-myc oncogene may be associated with unfavourable prognosis of thyroid carcinoma. It has been shown that the activated c-myc oncogene may play an important role in the initiation and progress of thyroid carcinoma.
采用分子杂交技术,对15例原发性甲状腺癌患者、3例甲状腺腺瘤患者的肿瘤组织以及5例正常甲状腺组织和1例相邻非肿瘤性甲状腺组织进行了C-myc癌基因结构与表达的分析。我们发现,15例癌症患者中有9例C-myc癌基因过度表达(即表达水平比正常甲状腺组织高3至11倍)。在4份癌症样本中观察到C-myc基因重排,其中1份样本显示C-myc基因扩增了150倍。C-myc基因的过度表达和扩增在预后更差、恶性程度更高的甲状腺癌患者中经常被检测到,这表明C-myc癌基因的过度表达、扩增和重排可能与甲状腺癌的不良预后有关。研究表明,激活的C-myc癌基因可能在甲状腺癌的发生和发展中起重要作用。