Ito T, Seyama T, Mizuno T, Tsuyama N, Hayashi T, Hayashi Y, Dohi K, Nakamura N, Akiyama M
Department of Radiobiology, Radiation Effects Research Foundation, Hiroshima, Japan.
Cancer Res. 1992 Mar 1;52(5):1369-71.
Thyroid neoplasms show a wide variety of lesions varying from slowly growing differentiated adenocarcinomas to rapidly proliferating undifferentiated carcinomas. There has been some histopathological evidence that the undifferentiated thyroid carcinomas are derived from differentiated carcinomas. Moreover, it is suspected that some genetic events might be associated with such changes. In the present study, mutations in the p53 gene were investigated by direct sequencing analysis after polymerase chain reaction amplification of exons 5 to 8, using paraffin-embedded primary tumors and cultured cells. No mutations in exons 5 to 8 were detected in 10 differentiated papillary adenocarcinomas, whereas 6 of 7 undifferentiated carcinomas were found to carry base substitution mutations. Sequencing analysis confirmed mutations at codons 135 (TGC----TGT), 141 (CCC----CCT), 178 (CAC----GAC), 213 (CGA----TGA), 248 (CGG----CAG, CGG----TGG), and 273 (CGT----TGT). The spectrum of mutations (G:C to A:T transitions in 7 of 8) might be a specific feature of the spontaneous cancers. The results strongly suggest that, in human thyroid glands, p53 mutations play a crucial role in the progression of differentiated carcinomas to undifferentiated ones.
甲状腺肿瘤表现出多种多样的病变,从生长缓慢的分化型腺癌到快速增殖的未分化癌。有一些组织病理学证据表明,未分化甲状腺癌源自分化型癌。此外,有人怀疑某些基因事件可能与这种变化有关。在本研究中,使用石蜡包埋的原发性肿瘤和培养细胞,通过聚合酶链反应扩增外显子5至8后进行直接测序分析,研究了p53基因的突变情况。在10例分化型乳头状腺癌中未检测到外显子5至8的突变,而在7例未分化癌中有6例发现携带碱基替代突变。测序分析证实了密码子135(TGC----TGT)、141(CCC----CCT)、178(CAC----GAC)、213(CGA----TGA)、248(CGG----CAG,CGG----TGG)和273(CGT----TGT)处的突变。突变谱(8例中有7例为G:C到A:T转换)可能是自发癌的一个特征。结果强烈表明,在人类甲状腺中,p53突变在分化型癌向未分化癌的进展中起关键作用。