Fusco Alfredo, Santoro Massimo
Dipartimento di Biologia e Patologia Cellulare e Molecolare, Istituto di Endocrinologia ed Oncologia Sperimentale, Facoltà di Medicina e Chirurgia di Napoli, Università degli Studi di Napoli, Naples, Italy.
Arq Bras Endocrinol Metabol. 2007 Jul;51(5):731-5. doi: 10.1590/s0004-27302007000500010.
The RET/PTC oncogene has been isolated almost twenty years ago. During these years, the research has given a final answer to several questions. In fact, it has been demonstrated that: a) RET/PTC is an early event in the process of thyroid carcinogenesis and has a critical role in the generation of the papillary carcinoma; b) RET/PTC activation is essentially restricted to the papillary histotype and to the Hürthle thyroid tumors; c) its incidence increases after exposure to radiations. However, some questions have not found a final answer yet: a) which is the real frequency of RET/PTC activation? Likely it is around 20%, but this point is still questionable; b) which other gene modifications are required to lead a thyroid cell carrying a RET/PTC oncogene to the malignant phenotype?, and c) is there any correlation between RET/PTC activation and clinical parameters? We hope that these questions will have a clear answer in the near future.
RET/PTC癌基因于近二十年前被分离出来。在这些年里,该研究对几个问题给出了最终答案。事实上,已经证明:a) RET/PTC是甲状腺癌发生过程中的一个早期事件,在乳头状癌的发生中起关键作用;b) RET/PTC激活基本上仅限于乳头状组织学类型和许特莱甲状腺肿瘤;c) 其发生率在接触辐射后会增加。然而,一些问题尚未找到最终答案:a) RET/PTC激活的实际频率是多少?可能约为20%,但这一点仍有疑问;b) 携带RET/PTC癌基因的甲状腺细胞要转变为恶性表型还需要哪些其他基因修饰?以及c) RET/PTC激活与临床参数之间是否存在关联?我们希望这些问题在不久的将来能有明确答案。