抗乳腺癌症药物筛选的统计研究

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引用次数: 0

摘要

癌症是最致命的癌症之一,雌激素受体α亚型(ERα)是其重要靶点。能够对抗ERα活性的化合物可能是治疗癌症的候选化合物。药物发现过程是一个非常庞大和复杂的过程,通常需要从大量化合物中选择一种。本文考虑了生物活性描述符的独立性、耦合性和相关性,从729个生物活性描述符中选择了15个最具潜在价值的生物活性描述符。将优化的反向传播神经网络用于ERα,通过梯度提升算法验证了所选15个生物活性描述符的药代动力学和安全性。结果表明,这15个生物活性描述符不仅能很好地拟合ERα活性的非线性关系,而且能准确预测其药代动力学特性和安全性,平均准确率为89.92~94.80%,具有很高的医学研究价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Statistical Study on Anti-Breast Cancer Drug Screening
Breast cancer is one of the most lethal cancers, estrogen receptor α Subtype (ERα) is an important target. The compounds that able to fight ERα active may be candidates for treatment of breast cancer. The drug discovery process is a very large and complex process that often requires one selected from a large number of compounds. This paper considers the independence, coupling, and relevance of bioactivity descriptors, selects the 15 most potentially valuable bioactivity descriptors from 729 bioactivity descriptors. An optimized back propagation neural network is used for ERα, the pharmacokinetics and safety of 15 selected bioactivity descriptors were verified by gradient lifting algorithm. The results showed that these 15 biological activity descriptors could not only fit well with the nonlinear relationship of ERα activity can also accurately predict its pharmacokinetic characteristics and safety, with an average accuracy of 89.92~94.80%. Therefore, these biological activity descriptors have great medical research value.
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