Ito Yasuhiro, Miyoshi Eiji, Uda Erika, Yoshida Hiroshi, Uruno Takashi, Takamura Yuuki, Miya Akihiro, Kobayashi Kaoru, Matsuzuka Fumio, Matsuura Nariaki, Kakudo Kennichi, Kuma Kanji, Miyauchi Akira
Department of Surgery, Kuma Hospital, 8-2-35, Shimoyamate-dori, Chuo-ku, Kobe 650-0011, Japan.
Cancer Lett. 2003 Oct 28;200(2):161-6. doi: 10.1016/s0304-3835(03)00282-9.
14-3-3 sigma is a negative regulator of the cell cycle and contributes to G2 arrest. Thus far, the lack of its expression due to hypermethylation of the CpG islands has been reported in some carcinomas. In this study, we investigated the expression of 14-3-3 sigma in thyroid neoplasms by means of immunohistochemistry as well as Western blot analysis. Normal follicules did not express 14-3-3 sigma. In 82 papillary carcinomas, all the cases expressed 14-3-3 sigma and its expression was not reduced but even enhanced in the advanced stage and in poorly differentiated types. Furthermore, 21 of the 23 anaplastic carcinomas expressed 14-3-3 sigma and its expression level tended to be higher than in papillary carcinoma. On the other hand, none of the 34 follicular carcinomas or 29 follicular adenomas expressed 14-3-3 sigma. These results suggest that 14-3-3 sigma plays a constitutive role in papillary carcinoma rather than acting as a cell cycle regulator, whereas it is not required for the occurrence and development of follicular tumor.
14-3-3σ是细胞周期的负调节因子,有助于G2期阻滞。迄今为止,在一些癌症中已报道由于CpG岛的高甲基化导致其表达缺失。在本研究中,我们通过免疫组织化学以及蛋白质印迹分析研究了14-3-3σ在甲状腺肿瘤中的表达。正常滤泡不表达14-3-3σ。在82例乳头状癌中,所有病例均表达14-3-3σ,其表达在晚期和低分化类型中不仅没有降低反而增强。此外,23例间变性癌中有21例表达14-3-3σ,其表达水平往往高于乳头状癌。另一方面,34例滤泡癌或29例滤泡性腺瘤均未表达14-3-3σ。这些结果表明,14-3-3σ在乳头状癌中起组成性作用,而不是作为细胞周期调节因子,而滤泡性肿瘤的发生和发展不需要它。