p53 and p21WAF1Expression in Lymphocytic Thyroiditis and Thyroid Tumors

Isao Okayasu , Toji Osakabe , Midori Onozawa , Tetuo Mikami , Mutsunori Fujiwara
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引用次数: 30

Abstract

To clarify the roles of increased apoptosis and cell proliferation in chronic autoimmune lymphocytic thyroiditis and thyroid tumorigenesis, expression of p53 and p21WAF1proteins was immunohistochemically investigated in a series of 158 cases. Positive epithelial cells were quantified to give numbers per unit square and to score for distribution. They were found scattered in nontumorous thyroid tissue, their numbers increasing with the severity of thyroiditis and the correlation between expression of the two proteins, regardless of the presence or absence of thyroid neoplasms. Simultaneous expression of both proteins was occasionally found in the same cells by analysis of serial histologic sections. In thyroid tumors, increased expression was found to be diffuse, focal, or scattered for the distribution of p53- or p21WAF1-immunopositive cells in accordance with tumor cell dedifferentiation, showing significant correlation between expression of the two proteins. Correlated with these findings, enhanced apoptosis along with decreased Bcl-2 expression and increased Ki-67 labeling in lymphocytic thyroiditis and thyroid tumors was also confirmed in the same series, usingin situDNA nick-end labeling and immunohistochemical methods. Increased expression of p53 and/or p21WAF1proteins was thus suggestive of possible DNA damage and increased apoptosis in autoimmune thyroiditis. In addition, a significant correlation between protein overexpression and dedifferentiation of thyroid tumor cells was apparent.

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p53和p21waf1在淋巴细胞性甲状腺炎和甲状腺肿瘤中的表达
为了阐明细胞凋亡和细胞增殖增加在慢性自身免疫性淋巴细胞性甲状腺炎和甲状腺肿瘤发生中的作用,我们对158例患者的p53和p21waf1蛋白的表达进行了免疫组织化学研究。阳性上皮细胞被量化,以给出每单位平方的数量,并对分布进行评分。它们分散在非肿瘤甲状腺组织中,它们的数量随着甲状腺炎的严重程度和这两种蛋白表达的相关性而增加,无论甲状腺肿瘤是否存在。通过对连续组织学切片的分析,在同一细胞中偶尔发现两种蛋白的同时表达。在甲状腺肿瘤中,p53-或p21waf1免疫阳性细胞根据肿瘤细胞去分化,呈弥漫性、局灶性或散在性分布,表达增加,两种蛋白表达显著相关。与这些发现相关的是,在同一系列中,使用situDNA镍端标记和免疫组织化学方法也证实了淋巴细胞性甲状腺炎和甲状腺肿瘤中凋亡增强、Bcl-2表达降低和Ki-67标记升高。因此,p53和/或p21waf1蛋白的表达增加提示自身免疫性甲状腺炎可能存在DNA损伤和细胞凋亡增加。此外,蛋白过表达与甲状腺肿瘤细胞去分化之间存在显著相关性。
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