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使用Kohonen自组织映射研究化疗药物的作用机制。

Use of the Kohonen self-organizing map to study the mechanisms of action of chemotherapeutic agents.

作者信息

van Osdol W W, Myers T G, Paull K D, Kohn K W, Weinstein J N

机构信息

Laboratory for Molecular Pharmacology, National Cancer Institute, Bethesda, Md 20892.

出版信息

J Natl Cancer Inst. 1994 Dec 21;86(24):1853-9. doi: 10.1093/jnci/86.24.1853.

Abstract

BACKGROUND

Many natural and synthetic compounds might prove to be effective in cancer chemotherapy. To identify potentially useful agents, the National Cancer Institute screens over 10,000 compounds annually against a panel of 60 distinct human tumor cell lines in vitro. This screening program generates large amounts of data that are organized into relational databases. Important questions concern the information content of the data and ways to extract that information. Previously, statistical techniques have revealed that compounds with similar patterns of activity against the 60 cell lines are often similar in structure and mechanism of action. Feed-forward, back-propagation neural networks have been trained on this type of data to predict broadly defined mechanisms of action of chemotherapeutic agents.

PURPOSE AND METHOD

In this report, we examine the information that can be extracted from the screening data by means of another type of neural network paradigm, the Kohonen self-organizing map. This is a topology-preserving function, obtained by unsupervised learning, that nonlinearly projects the high-dimensional activity patterns into two dimensions. Our dataset is almost identical to that used in the earlier neural network study.

RESULTS

The self-organizing maps we constructed have several important characteristics. 1) They partition the two-dimensional array into distinct regions, each of which is principally occupied by agents having the same broadly defined mechanism of action. 2) These regions can be resolved into distinct subregions that conform to plausible submechanisms and chemically defined subgroups of submechanism. 3) These results (and exceptions to them) are consistent with those obtained with the use of such deterministic measures of similarity among activity patterns as the Euclidean distance or Pearson correlation coefficient.

CONCLUSIONS

Our results indicate that the activity patterns obtained from the screen contain detailed information about mechanism of action and its basis in chemical structure. The self-organizing map can be used to suggest the mechanism of action of compounds identified by the screen as potentially useful chemotherapeutic agents and to probe the biology of the cell lines in the cancer screen. Kohonen self-organizing maps, unlike the previously applied neural networks, preserve and reveal the relationships among compounds acting by similar mechanisms and therefore have the potential to identify compounds that act by novel cytotoxic mechanisms.

摘要

背景

许多天然和合成化合物可能在癌症化疗中被证明是有效的。为了识别潜在有用的药物,美国国立癌症研究所每年在体外针对一组60种不同的人类肿瘤细胞系筛选超过10000种化合物。这个筛选项目产生了大量的数据,并被组织成关系数据库。重要的问题涉及数据的信息内容以及提取该信息的方法。此前,统计技术表明,对60种细胞系具有相似活性模式的化合物在结构和作用机制上通常相似。前馈、反向传播神经网络已针对此类数据进行训练,以预测化疗药物的广义作用机制。

目的和方法

在本报告中,我们研究了通过另一种神经网络范式——科霍宁自组织映射,能够从筛选数据中提取的信息。这是一种通过无监督学习获得的拓扑保持函数,它将高维活性模式非线性地投影到二维空间。我们的数据集几乎与早期神经网络研究中使用的数据集相同。

结果

我们构建的自组织映射具有几个重要特征。1) 它们将二维阵列划分为不同的区域,每个区域主要由具有相同广义作用机制的药物占据。2) 这些区域可以进一步分解为符合合理子机制和化学定义的子机制亚组的不同子区域。3) 这些结果(以及它们的例外情况)与使用诸如欧几里得距离或皮尔逊相关系数等活性模式之间相似性的确定性度量所获得的结果一致。

结论

我们的结果表明,从筛选中获得的活性模式包含有关作用机制及其化学结构基础的详细信息。自组织映射可用于推断筛选中鉴定为潜在有用化疗药物的化合物的作用机制,并探究癌症筛选中细胞系的生物学特性。与先前应用的神经网络不同,科霍宁自组织映射保留并揭示了通过相似机制起作用的化合物之间的关系,因此有潜力识别通过新型细胞毒性机制起作用的化合物。

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