Bass R A, Hemstreet G P, Honker N A, Hurst R E, Doggett R S
Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City 73190.
Int J Cancer. 1987 Nov 15;40(5):698-705. doi: 10.1002/ijc.2910400522.
A semi-automated quantitative fluorescence image analysis (QFIA) technique was developed with the Leitz TAS-Plus to detect bladder cancer using hyperploidy in urinary cells. Absolute nuclear fluorescence intensity (ANFI) (emission at 540 nm with excitation at 436 nm) of individual acridine-orange-stained cells was quantitated using (1) QFIA and (2) simple filter microspectrofluorophotometry (SFM). Both methods employed an internal phosphor particle standard which, when once calibrated against the DNA content of normal cells, obviates the necessity of routinely calibrating against normal cells in each sample. Results of SFM and QFIA were compared with routine Papanicolaou (Pap) cytopathology, using histopathology as the diagnostic standard in 272 samples from 67 symptomatic patients. The sensitivities for detecting low-grade transitional-cell carcinoma were 86% for SFM, 76% for QFIA, and 33% for Pap cytology. QFIA and SFM were significantly more sensitive at detecting bladder cancer than was Pap (0.01 greater than p greater than 0.001). Comparison of sensitivity obtained with bladder washings and urine samples showed that noninvasively obtained urines can be used. ANFI also detected recurrent and precancerous bladder lesions and kidney, ureter, and prostate lesions. This approach may prove generally useful in quantifying biochemical and immunological probes and should be broadly applicable as a research tool for studying the relationship of biochemical markers in the pathogenesis of disease and as a test for cancer control.
利用Leitz TAS-Plus开发了一种半自动定量荧光图像分析(QFIA)技术,通过检测尿细胞中的超倍体来诊断膀胱癌。使用(1)QFIA和(2)简单滤光片显微分光荧光光度法(SFM)对吖啶橙染色的单个细胞的绝对核荧光强度(ANFI)(激发波长436nm,发射波长540nm)进行定量。两种方法均采用内部磷光体颗粒标准,该标准一旦根据正常细胞的DNA含量进行校准,就无需对每个样本中的正常细胞进行常规校准。将SFM和QFIA的结果与常规巴氏(Pap)细胞病理学结果进行比较,以组织病理学作为诊断标准,对67例有症状患者的272个样本进行分析。检测低级别移行细胞癌的敏感度,SFM为86%,QFIA为76%,Pap细胞学为33%。QFIA和SFM在检测膀胱癌方面的敏感度显著高于Pap(0.01>p>0.001)。对膀胱冲洗液和尿液样本的敏感度比较表明,可使用非侵入性获取的尿液。ANFI还可检测复发性和癌前膀胱病变以及肾脏、输尿管和前列腺病变。这种方法可能在生化和免疫探针定量方面普遍有用,并且作为研究疾病发病机制中生化标志物关系的研究工具以及癌症控制检测手段应具有广泛的适用性。