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非霍奇金淋巴瘤中DNA含量和细胞大小的流式分析

Flow analysis of DNA content and cell size in non-Hodgkin's lymphoma.

作者信息

Diamond L W, Braylan R C

出版信息

Cancer Res. 1980 Mar;40(3):703-12.

PMID:7471089
Abstract

Cellular DNA content, Coulter volume, and light scatter were measured in cell suspensions from 30 non-Hodgkin's lymphomas in order to assess flow analysis as a quantitative and reproducible means of evaluating these diseases. Nonneoplastic control populations included 31 samples obtained from lymph nodes, spleens, tonsils, and peripheral blood. Cellular DNA and light scatter were measured on ethanol-fixed cells by flow microfluorometry using nuclei isolated from chicken erythrocytes as an internal standard. For DNA analysis, the cells were stained with propidium iodide following RNase treatment. The cellular DNA content of the human populations was expressed as a ratio between the DNA content of the human G0-G1 cells and that of the chicken erythrocyte nuclei. The mean DNA ratio for the 31 nonneoplastic samples was 2.83 +/- 0.08 (S.D.) In these samples, the coefficient of variation of the human G0-G1 peak ranged from 2.27 to 3.63% (mean 3.09 +/- 0.32%). Fifteen of 30 non-Hodgkin's lymphomas, including 7 of 15 low-grade lymphomas and 8 of 15 high-grade lymphomas, had abnormal DNA content, the majority containing hyperdiploid G0-G1 populations. In six malignant lymphomas with normal DNA content, the coefficient of variation of the human G0-G1 peak, corrected for differences in instrument setting was greater than that seen in the nonneoplastic populations. A good correlation between the percentage of cells calculated to be in the S phase of the cell cycle and the expected clinical behavior of the tumors was observed. In those lymphomas in which the S-phase percentages could be calculated, 11 of 13 low-grade lymphomas had less than 5% of the cells in S phase, and 7 of 10 high-grade lymphomas had greater than 5% of the cells in S phase. Thirteen of 21 neoplastic cases in which Coulter volume determinations were performed could be distinguished from the nonneoplastic controls on the basis of their modal volume. Although some correlation was observed between light scatter of ethanol-fixed cells and Coulter volume measurements on unfixed cells, light scatter was found to be less discriminatory. Altogether, by all three flow parameters studied, 26 of 30 (87%) of the neoplastic cases could be distinguished from nonneoplastic controls.

摘要

为了评估流式细胞分析作为一种定量且可重复的评估这些疾病的方法,对30例非霍奇金淋巴瘤的细胞悬液进行了细胞DNA含量、库尔特体积和光散射的测量。非肿瘤对照群体包括从淋巴结、脾脏、扁桃体和外周血获取的31个样本。通过流式微量荧光测定法,以从鸡红细胞分离的细胞核作为内标,对乙醇固定的细胞进行细胞DNA和光散射的测量。对于DNA分析,细胞经核糖核酸酶处理后用碘化丙啶染色。人类群体的细胞DNA含量以人类G0-G1期细胞的DNA含量与鸡红细胞核的DNA含量之比表示。31个非肿瘤样本的平均DNA比值为2.83±0.08(标准差)。在这些样本中,人类G0-G1峰的变异系数范围为2.27%至3.63%(平均3.09±0.32%)。30例非霍奇金淋巴瘤中有15例,包括15例低级别淋巴瘤中的7例和15例高级别淋巴瘤中的8例,其DNA含量异常,大多数含有超二倍体G0-G1群体。在6例DNA含量正常的恶性淋巴瘤中,校正仪器设置差异后,人类G0-G1峰的变异系数高于非肿瘤群体。观察到计算得出的处于细胞周期S期的细胞百分比与肿瘤预期临床行为之间存在良好相关性。在那些可以计算S期百分比的淋巴瘤中,13例低级别淋巴瘤中有11例S期细胞少于5%,10例高级别淋巴瘤中有7例S期细胞多于5%。在进行了库尔特体积测定的21例肿瘤病例中,有13例可以根据其众数体积与非肿瘤对照区分开来。尽管观察到乙醇固定细胞的光散射与未固定细胞的库尔特体积测量之间存在一定相关性,但发现光散射的鉴别能力较差。总体而言,通过所研究的所有三个流式参数,30例肿瘤病例中有26例(87%)可以与非肿瘤对照区分开来。

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