Facoetti A, Ranza E, Benericetti E, Ceroni M, Tedeschi F, Nano R
Dipartimento di Biologia Animale, Università di Pavia, Pavia, Italy.
Anticancer Res. 2006 Mar-Apr;26(2A):1071-5.
At present there is increasing evidence concerning the value of minichromosome maintenance (MCM) protein expression as a novel indicator of proliferation. In the present study, 15 glioblastoma samples, classified according to WHO, were analysed to evaluate the expression of the principal proliferation markers. The samples examined were subdivided into 2 cytological subsets, small cell (SC) or multiforme cell (MC) glioblastoma, according to the predominant cell type defined in individual specimens. MCM7 detected more cells in the cycle than Ki67 and PCNA and all cases of SC glioblastoma, the most aggressive subset, displayed a significant increase of MCM7-stained nuclei versus those stained with Ki67. These results suggest that the cell cycle-associated proteins MCM are not only useful markers of proliferation, but also valid aids for diagnosis in cerebral glioblastoma.
目前,关于微小染色体维持(MCM)蛋白表达作为一种新的增殖指标的价值,有越来越多的证据。在本研究中,对15例根据世界卫生组织(WHO)分类的胶质母细胞瘤样本进行分析,以评估主要增殖标志物的表达。根据各个标本中定义的主要细胞类型,将所检查的样本细分为2个细胞学亚组,即小细胞(SC)或多形细胞(MC)胶质母细胞瘤。MCM7检测到的处于细胞周期中的细胞比Ki67和PCNA更多,并且所有SC胶质母细胞瘤病例(最具侵袭性的亚组)与Ki67染色的细胞核相比,MCM7染色的细胞核显著增加。这些结果表明,细胞周期相关蛋白MCM不仅是有用的增殖标志物,而且对脑胶质母细胞瘤的诊断也有有效的辅助作用。