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首页> 外文期刊>Pathobiology: journal of immunopathology, molecular and cellular biology >Frequent Upregulation of Cyclin D1 and p16 Expression with Low Ki-67 Scores in Multinucleated Giant Cells.
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Frequent Upregulation of Cyclin D1 and p16 Expression with Low Ki-67 Scores in Multinucleated Giant Cells.

机译:多核巨细胞中Cyclin D1和p16表达的频繁上调,Ki-67评分低。

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摘要

Background/Aims: Multinucleated giant cells are formed from the fusion of macrophages and are classified into foreign body-type giant cells (FBGCs), osteoclast-type giant cells (OCGCs) and Langhans-type giant cells (LHGCs). OCGCs display upregulated cyclin D1 expression with low Ki-67 activity. However, little is known about the expression of cell cycle regulators in the other types of multinucleated giant cells. We aimed to investigate the cell cycle status of multinucleated giant cells. Methods: The immunohistochemical expressions of cyclin D1, p16(INK4a) and Ki-67 were analyzed in a total of 127 cases showing multinucleated giant cells. Results: Cyclin D1 was overexpressed in 45 (88%) of 51 FBGC cases, 25 (86%) of 29 OCGC cases and 22 (47%) of 47 LHGC cases. p16(INK4a) showed diffuse nuclear and/or cytoplasmic overexpression in 45 (88%) of 51 FBGC cases, 27 (93%) of 29 OCGC cases and 24 (51%) of 47 LHGC cases. Ki-67 immunostaining was negative in almost all FBGC, OCGC and LHGC cases. Conclusion: This study demonstrates that FBGCs and OCGCs frequently show upregulation of cyclin D1 and p16(INK4a) expression with low Ki-67 scores. This suggests that multinucleated giant cells are arrested in the G1/S cell cycle transition.
机译:背景/目的:多核巨细胞由巨噬细胞融合形成,分为异物型巨细胞(FBGC),破骨细胞型巨细胞(OCGC)和朗汉斯型巨细胞(LHGC)。 OCGC显示上调的细胞周期蛋白D1表达,且Ki-67活性较低。但是,关于细胞周期调节剂在其他类型的多核巨细胞中的表达知之甚少。我们旨在研究多核巨细胞的细胞周期状态。方法:分析127例多核巨细胞中cyclin D1,p16(INK4a)和Ki-67的免疫组织化学表达。结果:Cyclin D1在51例FBGC患者中过表达(88%),29例OCGC患者中25例(86%)和47例LHGC患者中过表达。 p16(INK4a)在51例FBGC病例中的45(88%),29例OCGC病例中的27(93%)和47例LHGC病例中显示了弥漫性核和/或细胞质过表达。几乎所有FBGC,OCGC和LHGC病例Ki-67免疫染色均为阴性。结论:这项研究表明,FBGC和OCGCs经常显示细胞周期蛋白D1和p16(INK4a)表达的上调,而Ki-67得分较低。这表明多核巨细胞在G1 / S细胞周期过渡中被阻滞。

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