Lipkin M
Cell Tissue Kinet. 1984 May;17(3):209-22. doi: 10.1111/j.1365-2184.1984.tb00582.x.
An analysis has been developed to improve the quantitation of abnormal patterns of tritiated thymidine [(3H]TdR) labelling of colonic epithelial cells, in biopsy specimens removed from human subjects at varying degrees of risk for colon cancer. After pulse incubation of specimens of colonic mucosa with [3H]TdR, each subject's microautoradiographic epithelial cell labelling distribution was segregated into eleven compartments over entire colonic crypts. The findings of each subject were then analysed to determine their relative degree of similarity to the findings for two reference populations of interest, i.e. a high-risk and a low-risk population; the individual was then classified as being closer to one or the other of the reference populations. The analysis developed is based upon a comparison of multinomial probabilities for the distributions of the labelled cells within the crypts, and permits the routine categorization of uneven distributions of labelled cells. For each subject, certain linear scores, a prognostic index based on them, and a related presumptive risk, were calculated. The sensitivity with which individuals known to be symptomatic for polyposis, and the specificity with which individuals known to be at lower risk were determined, were 73 and 93% respectively. The results suggest that this method of distinguishing among integer distributions of [3H]TdR- labelled cells in biopsies of colonic mucosa, may provide a useful basis for identifying individuals with familial polyposis, by separating their labelling patterns from those of low-risk subjects.
已开发出一种分析方法,用于改进对从处于不同结肠癌风险程度的人类受试者身上获取的活检标本中结肠上皮细胞氚标记胸腺嘧啶核苷[(3H]TdR)标记异常模式的定量分析。在用[3H]TdR对结肠黏膜标本进行脉冲孵育后,将每个受试者的显微放射自显影上皮细胞标记分布在整个结肠隐窝中分为11个区室。然后分析每个受试者的结果,以确定其与两个感兴趣的参考人群(即高风险人群和低风险人群)的结果的相对相似程度;然后将个体分类为更接近其中一个参考人群。所开发的分析方法基于对隐窝内标记细胞分布的多项概率的比较,并允许对标记细胞的不均匀分布进行常规分类。为每个受试者计算了某些线性分数、基于这些分数的预后指数以及相关的推定风险。已知有息肉病症状的个体的敏感性和已知风险较低的个体的特异性分别为73%和93%。结果表明,这种区分结肠黏膜活检中[3H]TdR标记细胞整数分布的方法,通过将其标记模式与低风险受试者的标记模式分开,可能为识别家族性息肉病个体提供有用的依据。