Wharton S B, Chan K K, Anderson J R, Stoeber K, Williams G H
Academic Unit of Pathology, University of Sheffield, Medical School, UK.
Neuropathol Appl Neurobiol. 2001 Aug;27(4):305-13. doi: 10.1046/j.0305-1846.2001.00333.x.
The grading and prognostic assessment of oligodendrogliomas is severely constrained and there remains a need for improved diagnosis. Recently, we have identified the minichromosome maintenance (MCM) family of proteins as a novel class of proliferation markers. Mcm2 is a protein which forms part of the prereplicative complex. It is necessary for this complex to be assembled at origins of future DNA replication during the G1 phase to allow genome replication in the subsequent S phase. Our aim was to determine whether analysis of Mcm2 protein expression in oligodendrogliomas is of diagnostic value. Immunohistochemical staining for Mcm2 was performed on an archival series of 32 oligodendrogliomas. These tumours have been previously characterized for Ki67, mitotic labelling index and outcome. Cells showing expression of Mcm2 were quantified as a percentage to provide an Mcm2 labelling index. We have demonstrated a good correlation between Mcm2 and Ki67 labelling indices (r = 0.76, P < 0.01) but immunohistochemistry for Mcm2 consistently identified a higher proportion of cells. Mcm2 labelling index was higher in grade III than grade II tumours (P < 0.001). Cases with a high Mcm2 labelling index showed a poorer prognosis than those with a low index (P = 0.497) in univariate analysis, but with wide variation in this small series. Demonstration of Mcm2 expression is of value to demonstrate the proliferative fraction of tumours and is likely to be of prognostic value. Its study in a larger series is therefore warranted.
少突胶质细胞瘤的分级和预后评估受到严重限制,仍然需要改进诊断方法。最近,我们已将微小染色体维持(MCM)蛋白家族鉴定为一类新型的增殖标志物。Mcm2是一种构成复制前复合体一部分的蛋白质。该复合体在G1期于未来DNA复制起点组装是后续S期进行基因组复制所必需的。我们的目的是确定分析少突胶质细胞瘤中Mcm2蛋白表达是否具有诊断价值。对32例少突胶质细胞瘤存档标本进行了Mcm2免疫组织化学染色。这些肿瘤先前已对Ki67、有丝分裂标记指数和预后进行了特征描述。对显示Mcm2表达的细胞进行定量,以百分比表示,从而得出Mcm2标记指数。我们已证明Mcm2与Ki67标记指数之间具有良好的相关性(r = 0.76,P < 0.01),但Mcm2免疫组织化学始终能鉴定出更高比例的细胞。Mcm2标记指数在III级肿瘤中高于II级肿瘤(P < 0.001)。在单因素分析中,Mcm2标记指数高的病例预后比指数低的病例差(P = 0.497),但在这个小样本系列中差异较大。Mcm2表达的显示对于证明肿瘤的增殖分数具有价值,并且可能具有预后价值。因此,有必要在更大的系列中对其进行研究。