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一组诊断性细胞病理学家对28种细胞系的肿瘤发生潜能进行细胞形态学评估。

Cytomorphologic evaluation of the neoplastic potential of 28 cell culture lines by a panel of diagnostic cytopathologists.

作者信息

Boone C W, Sanford K K, Frost J K, Mantel N, Gill G W, Jones G M

出版信息

Int J Cancer. 1986 Sep 15;38(3):361-7. doi: 10.1002/ijc.2910380310.

DOI:10.1002/ijc.2910380310
PMID:3744590
Abstract

A panel of 7 diagnostic cytopathologists, i.e., physicians trained to diagnose the malignant potential of human cells in Papanicolaou-stained smears, was asked to evaluate two sets of microscope slides of stained coverslip preparations of 28 cell culture lines, 15 of which were neoplastic. Slide Set I consisted of 13 pairs of cell lines, one member of each pair being nontumorigenic and the other tumorigenic; the lines were of mouse (9 pairs), rat (3 pairs), and human (1 pair) origin. Slide Set II contained 4 human lines: one lung cancer, one melanoma, and two fibroblast lines. Of a total of 114 diagnostic decisions by the panel, 88 were correct (66/86, 77%) in choosing which member of a pair was neoplastic and 22 were correct (22/28, 79%) in choosing whether a given individual human line was or was not neoplastic. Two members of the panel were correct more frequently, with 16/17 (94%) correct diagnoses, each. Five nuclear morphologic criteria of malignancy used by cytopathologists were prominent in the tumorigenic lines: altered chromatin pattern characterized by increasing size of chromatin granules and chromatin clumping, sharp angularity of large nucleolar and/or chromocenter borders with spicule formation (pointed projection), irregular parachromatin clearing (increase in the clarity of the clear spaces between chromatin threads, granules and clumps), uneven thickness of chromatin at the nuclear border, and variability in nuclear size and shape from cell to cell. These markers of neoplastic transformation, when added to those previously reported, should increase overall accuracy in the diagnosis of neoplastic transformation of mammalian cells in culture.

摘要

由7名诊断性细胞病理学家组成的小组(即接受过在巴氏染色涂片中诊断人类细胞恶性潜能培训的医生)被要求评估两组显微镜载玻片,这些载玻片是28种细胞系的染色盖玻片制备物,其中15种是肿瘤性的。第一组载玻片由13对细胞系组成,每对中的一个成员是非致瘤性的,另一个是致瘤性的;这些细胞系分别来源于小鼠(9对)、大鼠(3对)和人类(1对)。第二组载玻片包含4种人类细胞系:一种肺癌细胞系、一种黑色素瘤细胞系和两种成纤维细胞系。在该小组总共114次诊断决策中,在选择一对细胞系中哪一个是肿瘤性的方面,88次正确(66/86,77%);在选择给定的单个人类细胞系是否为肿瘤性方面,22次正确(22/28,79%)。该小组的两名成员诊断正确率更高,各自为16/17(94%)。细胞病理学家使用的五种恶性核形态学标准在致瘤性细胞系中很突出:染色质模式改变,其特征为染色质颗粒大小增加和染色质聚集;大核仁及/或染色中心边界呈尖锐角状并伴有针状形成(尖状突起);不规则的副染色质清除(染色质丝、颗粒和团块之间透明空间的清晰度增加);核边界处染色质厚度不均匀;以及细胞与细胞之间核大小和形状的变异性。这些肿瘤转化标志物,加上先前报道的那些标志物,应该会提高培养的哺乳动物细胞肿瘤转化诊断的总体准确性。

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