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甲状腺恶性淋巴瘤中Cdc25A和cdc25B的表达:与组织学亚型及细胞增殖的相关性

Cdc25A and cdc25B expression in malignant lymphoma of the thyroid: correlation with histological subtypes and cell proliferation.

作者信息

Ito Yasuhiro, Yoshida Hiroshi, Matsuzuka Fumio, Matsuura Nariaki, Nakamura Yasushi, Nakamine Hirokazu, Kakudo Kennichi, Kuma Kanji, Miyauchi Akira

机构信息

Department of Surgery, Kuma Hospital, Chuo-ku, Kobe 650-0011, Japan.

出版信息

Int J Mol Med. 2004 Mar;13(3):431-5.

Abstract

Cdc25B and cdc25A phosphatases are representative stimulators of cell cycle progression, and recent studies have also indicated their oncogenic roles. In this study, we investigated the expression of these phosphatases in malignant lymphoma of the thyroid by immunohistochemistry. These phosphatases were not expressed in follicular cells in normal follicles, but were heterogeneously or diffusely expressed in the follicles in chronic thyroiditis and malignant lymphoma. In infiltrating lymphocytes in chronic thyroiditis, they were only occasionally expressed. Of the 47 cases of lymphoma, 30 (63.8%) were classified as high group for cdc25B because it was expressed in more than 25% of lymphoma cells. Cdc25B expression level was inversely associated with MIB-1 labeling index (p=0.0008), and aberrant p53 expression (p=0.0077). Furthermore, cases of marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MZBL) were more frequently classified as high group (p=0.0318) than those of diffuse large B-cell lymphoma (DLBL). On the other hand, 22 cases (46.8%) were regarded as high group for cdc25A, but its expression level was not linked to those parameters. These findings suggest that i) cdc25B plays a role in the early phase of thyroid lymphoma possibly including the malignant transformation from chronic thyroiditis, and ii) cdc25A may contribute to the progression of lymphoma.

摘要

细胞周期蛋白磷酸酶25B(Cdc25B)和细胞周期蛋白磷酸酶25A(Cdc25A)是细胞周期进程的代表性刺激因子,近期研究还表明了它们的致癌作用。在本研究中,我们通过免疫组织化学法调查了这些磷酸酶在甲状腺恶性淋巴瘤中的表达情况。这些磷酸酶在正常滤泡的滤泡细胞中不表达,但在慢性甲状腺炎和恶性淋巴瘤的滤泡中呈异质性或弥漫性表达。在慢性甲状腺炎的浸润淋巴细胞中,它们只是偶尔表达。在47例淋巴瘤病例中,30例(63.8%)因Cdc25B在超过25%的淋巴瘤细胞中表达而被归类为高表达组。Cdc25B表达水平与MIB-1标记指数呈负相关(p = 0.0008),与p53异常表达也呈负相关(p = 0.0077)。此外,黏膜相关淋巴组织边缘区B细胞淋巴瘤(MZBL)病例比弥漫性大B细胞淋巴瘤(DLBL)病例更频繁地被归类为高表达组(p = 0.0318)。另一方面,22例(46.8%)被视为Cdc25A高表达组,但其表达水平与这些参数无关。这些发现表明,i)Cdc25B可能在甲状腺淋巴瘤的早期阶段发挥作用,可能包括从慢性甲状腺炎的恶性转化;ii)Cdc25A可能有助于淋巴瘤的进展。

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