Cormanich Rodrigo A, Goodarzi Mohammad, Freitas Matheus P
Departamento de Química, Universidade Federal de Lavras, CP 3037, 37200-000 Lavras, MG, Brazil.
Chem Biol Drug Des. 2009 Feb;73(2):244-52. doi: 10.1111/j.1747-0285.2008.00764.x.
Inhibition of tyrosine kinase enzyme WEE1 is an important step for the treatment of cancer. The bioactivities of a series of WEE1 inhibitors have been previously modeled through comparative molecular field analyses (CoMFA and CoMSIA), but a two-dimensional image-based quantitative structure-activity relationship approach has shown to be highly predictive for other compound classes. This method, called multivariate image analysis applied to quantitative structure-activity relationship, was applied here to derive quantitative structure-activity relationship models. Whilst the well-known bilinear and multilinear partial least squares regressions (PLS and N-PLS, respectively) correlated multivariate image analysis descriptors with the corresponding dependent variables only reasonably well, the use of wavelet and principal component ranking as variable selection methods, together with least-squares support vector machine, improved significantly the prediction statistics. These recently implemented mathematical tools, particularly novel in quantitative structure-activity relationship studies, represent an important advance for the development of more predictive quantitative structure-activity relationship models and, consequently, new drugs.
抑制酪氨酸激酶WEE1是癌症治疗的重要一步。此前已通过比较分子场分析(CoMFA和CoMSIA)对一系列WEE1抑制剂的生物活性进行建模,但基于二维图像的定量构效关系方法已被证明对其他化合物类别具有高度预测性。这种称为应用于定量构效关系的多变量图像分析的方法在此处用于推导定量构效关系模型。虽然著名的双线性和多线性偏最小二乘回归(分别为PLS和N-PLS)仅能使多变量图像分析描述符与相应的因变量有合理的相关性,但使用小波和主成分排序作为变量选择方法,再结合最小二乘支持向量机,显著改善了预测统计结果。这些最近实施的数学工具,在定量构效关系研究中尤其新颖,代表了开发更具预测性的定量构效关系模型以及新药物方面的重要进展。