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通过计算机辅助显微镜生成的定量形态核变量对胶质母细胞瘤中的星形胶质细胞与少突胶质细胞表型进行表征。

Characterization of astroglial versus oligodendroglial phenotypes in glioblastomas by means of quantitative morphonuclear variables generated by computer-assisted microscopy.

作者信息

Decaestecker C, Camby I, Gordower L, Dewitte O, Cras P, Martin J J, Pasteels J L, Van Ham P, Brotchi J, Kiss R, Salmon I

机构信息

Laboratory of Histology, Faculty of Applied Sciences, the Université Libre de Bruxelles, Brussels, Belgium.

出版信息

J Neuropathol Exp Neurol. 1998 Aug;57(8):791-802. doi: 10.1097/00005072-199808000-00008.

Abstract

The current WHO classification places glioblastomas in the astrocytoma category. However, whether or not glioblastomas also show oligodendroglial differentiation remains a matter of controversy. This study investigates, at the morphonuclear level, the hypothesis that some glioblastomas (GBMs) may also represent the ultimate level of malignancy in the oligodendroglial lineage. Using a series of 164 GBMs, we sought to ascertain whether any of these GBMs exhibited phenotypical characteristics that were more closely related to oligodendroglial lineages than astrocytic lineages. Phenotypical features were quantitatively determined by means of the computer-assisted microscope analysis of Feulgen-stained nuclei, a process that made it possible to quantitatively describe the patterns of the cell nuclei (and, more specifically, of their chromatin) through 16 variables, and the distribution of the nuclear DNA content (DNA ploidy) through 8 variables. The phenotypical characteristics typical of astrocytic and oligodendroglial tumors were analyzed by means of Discriminant Analysis, a statistical multivariate analysis, performed on a series of 65 astrocytic and oligodendroglial tumors. This series consisted of 14 WHO grade II and 19 grade III astrocytomas and 24 WHO grade II and 8 grade III oligodendrogliomas. This multivariate analysis enabled an accurate model to be produced that distinguished between astrocytomas and oligodendrogliomas on the basis of 5 cytometry-generated variables. This model was used to characterize the phenotype of each of the 164 glioblastomas. The results show that of these 164 glioblastomas, 6 (about 3.5%) displayed phenotypes that were very similar to oligodendrogliomas, and 141 displayed phenotypes that were very similar to astrocytomas. The phenotypes of the 17 remaining GBMs were too ambiguous to be categorized as having a pure astrocytic or oligodendroglial lineage.

摘要

世界卫生组织(WHO)目前的分类将胶质母细胞瘤归为星形细胞瘤类别。然而,胶质母细胞瘤是否也显示少突胶质细胞分化仍存在争议。本研究在形态核水平上调查了一种假说,即某些胶质母细胞瘤(GBM)可能也代表少突胶质细胞谱系中的恶性肿瘤终末阶段。我们使用了一系列164例胶质母细胞瘤,试图确定这些胶质母细胞瘤中是否有任何肿瘤表现出与少突胶质细胞谱系比星形细胞谱系更密切相关的表型特征。通过对福尔根染色细胞核进行计算机辅助显微镜分析来定量确定表型特征,该过程使得能够通过16个变量定量描述细胞核(更具体地说是其染色质)的模式,并通过8个变量描述核DNA含量(DNA倍性)的分布。通过判别分析对一系列65例星形细胞和少突胶质细胞肿瘤进行了典型的星形细胞和少突胶质细胞肿瘤表型特征分析,判别分析是一种统计多变量分析。该系列包括14例WHO二级和19例三级星形细胞瘤以及24例WHO二级和8例三级少突胶质细胞瘤。这种多变量分析能够生成一个准确的模型,该模型基于5个细胞计数产生的变量区分星形细胞瘤和少突胶质细胞瘤。该模型用于表征164例胶质母细胞瘤中每一例的表型。结果显示,在这164例胶质母细胞瘤中,6例(约3.5%)表现出与少突胶质细胞瘤非常相似的表型,141例表现出与星形细胞瘤非常相似的表型。其余17例胶质母细胞瘤的表型过于模糊,无法归类为具有纯星形细胞或少突胶质细胞谱系。

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