Remmelink M, Decaestecker C, Darro F, Goldschmidt D, Gebhart M, Pasteels J L, Kiss R, Salmon I
Laboratory of Histology, Faculty of Medicine, Free University of Brussels (ULB), Belgium.
J Cancer Res Clin Oncol. 1998;124(3-4):155-64. doi: 10.1007/s004320050149.
Little is known about the regulation of sarcoma proliferation by hormones and/or growth factors. We therefore characterised the in vitro proliferative influence on eight sarcoma cell lines of the platelet-derived growth factor, the insulin-like growth factor 1, triiodothyronine, the epidermal growth factor, the luteinising-hormone-releasing hormone, progesterone, gastrin and 17 beta-oestradiol. The influence of the different factors on the proliferation of sarcoma cell lines was measured by the colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test. Two culture media were studied: (1) a nutritionally poor medium containing 2% of fetal calf serum and (2) a nutritionally rich one containing 5% or 10% FCS both with and without the addition of non-essential amino acids. The results were analysed either by conventional statistical analyses or by a classification method based on a decision-tree approach developed in Machine Learning. This latter method was also compared to other classifiers (such as logistic regression and k nearest neighbours) with respect to its accuracy of classification. Monovariate statistical analysis showed that each of the eight cell lines exhibited sensitivity to at least one factor, and each factor significantly modified the proliferation of five or six of the eight cell lines under study. Of these eight lines one of fibrosarcoma origin was the most "factor-sensitive". Decision-tree-related data analysis enabled the specific pattern of factor sensitivity to be characterised for the three histological types of cell line under study. The effects of hormone and growth factors are significantly influenced by the type of culture medium used. The method used appeared to be an accurate classifier for the kind of data analysed. Sarcoma proliferation can be modulated, at least in vitro, by various hormones and growth factors, and the proliferation of each histopathological type exhibited a distinct sensitivity to different hormone and/or growth-factors.
关于激素和/或生长因子对肉瘤增殖的调节作用,目前所知甚少。因此,我们研究了血小板衍生生长因子、胰岛素样生长因子1、三碘甲状腺原氨酸、表皮生长因子、促黄体激素释放激素、孕酮、胃泌素和17β-雌二醇对8种肉瘤细胞系的体外增殖影响。通过比色法3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐试验来测定不同因子对肉瘤细胞系增殖的影响。研究了两种培养基:(1) 含有2%胎牛血清的营养贫乏培养基;(2) 含有5%或10%胎牛血清且添加或不添加非必需氨基酸的营养丰富培养基。结果通过传统统计分析或基于机器学习中开发的决策树方法的分类方法进行分析。还将后一种方法与其他分类器(如逻辑回归和k最近邻)在分类准确性方面进行了比较。单变量统计分析表明,8种细胞系中的每一种对至少一种因子都表现出敏感性,并且每种因子都显著改变了所研究的8种细胞系中5种或6种的增殖。在这8种细胞系中,一种纤维肉瘤来源的细胞系是最“因子敏感”的。与决策树相关的数据分析能够确定所研究的三种组织学类型细胞系的因子敏感性特定模式。激素和生长因子的作用受到所用培养基类型的显著影响。所使用的方法似乎是所分析数据类型的准确分类器。至少在体外,肉瘤增殖可被多种激素和生长因子调节,并且每种组织病理学类型的增殖对不同激素和/或生长因子表现出不同的敏感性。