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Cyclin D2 在慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的增殖中心过表达。

Cyclin D2 is overexpressed in proliferation centers of chronic lymphocytic leukemia/small lymphocytic lymphoma.

机构信息

Department of Pathology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

出版信息

Cancer Sci. 2011 Nov;102(11):2103-7. doi: 10.1111/j.1349-7006.2011.02046.x. Epub 2011 Aug 24.

Abstract

The D cyclins are important cell cycle regulatory proteins involved in the pathogenesis of some lymphomas. Cyclin D1 overexpression is a hallmark of mantle cell lymphoma, whereas cyclins D2 and D3 have not been shown to be closely associated with any particular subtype of lymphoma. In the present study, we found that cyclin D2 was specifically overexpressed in the proliferation centers (PC) of all cases of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) examined (19/19). To examine the molecular mechanisms underlying this overexpression, we immunohistochemically examined the expression of nuclear factor (NF)-κB, p15, p16, p18, and p27 in the PC of six patients. Five cases showed upregulation of NF-κB expression, which is known to directly induce cyclin D2 by binding to the promoter region of CCND2. All six PC examined demonstrated downregulation of p27 expression. In contrast, upregulation of p15 expression was detected in five of six PC examined. This discrepancy suggests that unknown cell cycle regulatory mechanisms involving NF-κB-related pathways are also involved, because NF-κB upregulates cyclin D2 not only directly, but also indirectly through c-Myc, which is believed to downregulate both p27 and p15. In conclusion, cyclin D2 is overexpressed in the PC of CLL/SLL and this overexpression is due, in part, to the upregulation of NF-κB-related pathways.

摘要

D 型细胞周期蛋白是参与某些淋巴瘤发病机制的重要细胞周期调控蛋白。Cyclin D1 过表达是套细胞淋巴瘤的一个标志,而 Cyclin D2 和 D3 与任何特定类型的淋巴瘤都没有密切关联。在本研究中,我们发现 Cyclin D2 在所有检查的慢性淋巴细胞白血病/小淋巴细胞淋巴瘤 (CLL/SLL) 的增殖中心 (PC) 中特异性过表达 (19/19)。为了研究这种过表达的分子机制,我们用免疫组织化学方法检查了 6 例患者 PC 中核因子 (NF)-κB、p15、p16、p18 和 p27 的表达。5 例显示 NF-κB 表达上调,NF-κB 通过与 CCND2 启动子区域结合直接诱导 Cyclin D2 表达。所有 6 例检查的 PC 均显示 p27 表达下调。相反,在 6 例检查的 PC 中,有 5 例检测到 p15 表达上调。这种差异表明,涉及 NF-κB 相关途径的未知细胞周期调控机制也参与其中,因为 NF-κB 不仅直接上调 Cyclin D2,还通过 c-Myc 间接上调 Cyclin D2,c-Myc 被认为下调 p27 和 p15。总之,Cyclin D2 在 CLL/SLL 的 PC 中过表达,这种过表达部分归因于 NF-κB 相关途径的上调。

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