Fujita F, Fujita M, Hirai T, Taguchi T
Gan To Kagaku Ryoho. 1987 Mar;14(3 Pt 1):618-25.
The chemosensitivity of human cancer lines is thought to be expressed as a result of contributions by various interacting factors. Multiple regression analyses were performed in order to clarify the weighting of factors responsible for the chemosensitivity of 15 human cancers xenografted into nude mice. Inhibition rates of 11 anticancer agents predetermined for each line of human cancer were used as the criterion variables. As the explanatory variables, 9 parameters characteristic of each cancer or cancer-bearing mouse were selected as follows; grade of differentiation, vascularity, percentage necrosis, volume doubling time, labeling index, LDH activity, tissue/serum LDH ratio, thymidine phosphorylase activity and serum CEA. By applying this analysis with stepwise deletion, the estimated multiple regression equations for drug sensitivity were clarified for each drug. Although all equations were composed of different factors and their partial repression coefficients varied from drug to drug, those among analogous drugs such as FT-207 and UFT, or MMC and M-83 had similar factors. The equations for M-83, ACNU and ADR consisted of a number of parameters with a sufficiently high coefficient of determination of over 80%. Even in cases of MXT that showed no significant factor upon simple correlation analysis, an equation with 7 factors revealed a coefficient of determination of 0.83. The estimated values of effectiveness for these drugs showed remarkable coincidence with each actual value. For some drugs, the in vivo mode of action was inferred through this analysis.
人类癌细胞系的化学敏感性被认为是多种相互作用因素共同作用的结果。为了阐明影响移植到裸鼠体内的15种人类癌症化学敏感性的因素权重,进行了多元回归分析。将针对每种人类癌症预先确定的11种抗癌药物的抑制率用作标准变量。作为解释变量,选择了以下9个每种癌症或荷瘤小鼠的特征参数:分化程度、血管生成、坏死百分比、体积倍增时间、标记指数、乳酸脱氢酶(LDH)活性、组织/血清LDH比值、胸苷磷酸化酶活性和血清癌胚抗原(CEA)。通过逐步剔除进行此分析,明确了每种药物的药物敏感性估计多元回归方程。尽管所有方程由不同因素组成,且其偏回归系数因药物而异,但类似药物(如FT - 207和UFT,或丝裂霉素C(MMC)和M - 83)之间具有相似因素。M - 83、阿糖胞苷(ACNU)和阿霉素(ADR)的方程由许多参数组成,决定系数足够高,超过80%。即使在简单相关分析中未显示出显著因素的丝裂霉素(MXT)的情况下,一个包含7个因素的方程显示决定系数为0.83。这些药物的有效性估计值与每个实际值显示出显著的一致性。通过此分析推断出了某些药物的体内作用模式。