Finding New VEGFR2 Inhibitors Using Support Vector Machine Classification Model

Nooshin Arabi, Mohammadreza Torabi, Afshin Fassihi, Fahimeh Ghasemi
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Abstract

Introduction: In our current era, the prevalence of cancer and its associated mortality rates have become a pressing concern. As such, finding effective methods for treating cancer has become a matter of significant importance. Abnormal angiogenesis is one of the common characteristics of different types of cancer. So far, the inhibition of vascular endothelial growth factor receptor 2 signaling pathway has received much attention due to its pro-angiogenic role. Therefore, finding reliable computational models to identify inhibitors can be effective in reducing time and cost. The purpose of this study was to use the support vector machine method to classify compounds into two inhibitory and non-inhibitory groups. Methods: In order to implement the machine learning model, the ligands studied in this research were extracted from the https://www.bindingdb.org database and after passing the necessary pre-processing, some filter-based and embedded feature selection methods were used.  After extracting the descriptors from the data, using the feature selection algorithm based on correlation, the dimensions of the data have been reduced in order to avoid overfitting the model. The classification task utilized a support vector machine model, employing various kernels such as Radial Basis Function (RBF), Polynomial, Sigmoid, and Linear. Results: The implementation of the support vector machine model with the RBF kernel along with the feature selection method based on correlation has resulted in a higher accuracy of 82.4% (P=0.008) compared to other feature selection methods used in this study. Conclusion: Observations indicate that the correlation-based feature selection method is more accurate than other methods used in this study.
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使用支持向量机分类模型寻找新的 VEGFR2 抑制剂
导 言在当今时代,癌症的发病率及其相关死亡率已成为一个亟待解决的问题。因此,寻找治疗癌症的有效方法已成为一个非常重要的问题。血管生成异常是不同类型癌症的共同特征之一。迄今为止,抑制血管内皮生长因子受体 2 信号通路因其促进血管生成的作用而备受关注。因此,寻找可靠的计算模型来确定抑制剂可以有效地减少时间和成本。本研究的目的是利用支持向量机方法将化合物分为抑制和非抑制两组。 方法:为了实现机器学习模型,本研究中的配体是从 https://www.bindingdb.org 数据库中提取的,在通过必要的预处理后,使用了一些基于过滤器和嵌入式特征选择方法。 从数据中提取描述符后,使用基于相关性的特征选择算法降低了数据维度,以避免模型过拟合。分类任务使用了支持向量机模型,并采用了径向基函数(RBF)、多项式、Sigmoid 和线性等各种核。 结果与本研究中使用的其他特征选择方法相比,使用 RBF 内核的支持向量机模型和基于相关性的特征选择方法的准确率更高,达到 82.4% (P=0.008)。 结论观察结果表明,基于相关性的特征选择方法比本研究中使用的其他方法更准确。
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