Drug Search and Design Considering Cell Specificity of Chemically Induced Gene Expression Profiles for Disease-Associated Tissues.

IF 2.8 4区 医学 Q3 CHEMISTRY, MEDICINAL
Chikashige Yamanaka, Michio Iwata, Kazuma Kaitoh, Yoshihiro Yamanishi
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引用次数: 0

Abstract

The use of omics data, including gene expression profiles, has recently gained increasing attention in drug discovery. Omics-based drug searches and designs are often based on the correlations between chemically induced and disease-induced gene expression profiles; however, the cell specificity has not been considered. In this study, we designed a novel computational method for drug search and design using cell-specific correlations between drugs and diseases. A data completion technique allowed the characterization of cell-specific gene expression patterns in diseased cells. This proposed method was applied to search for drug candidates and generate new chemical structures for gastric cancer and atopic dermatitis. The results of drug search demonstrated that compounds with diverse chemical structures were detected and were associated with target diseases at the molecular pathway levels. The results of drug design also demonstrated that newly generated compounds were reasonable in terms of the reproducibility of registered drugs. The proposed method is expected to be useful for omics-based drug discovery.

考虑疾病相关组织化学诱导基因表达谱细胞特异性的药物搜索和设计。
使用组学数据,包括基因表达谱,最近在药物发现中获得了越来越多的关注。基于组学的药物搜索和设计通常基于化学诱导和疾病诱导的基因表达谱之间的相关性;然而,细胞特异性尚未被考虑。在这项研究中,我们设计了一种新的计算方法,用于药物和疾病之间的细胞特异性相关性的药物搜索和设计。数据完成技术允许表征细胞特异性基因表达模式的病变细胞。该方法已应用于胃癌和特应性皮炎的候选药物的寻找和新的化学结构的生成。药物搜索结果表明,在分子途径水平上发现了具有多种化学结构的化合物,并与目标疾病相关。药物设计的结果也表明,新生成的化合物在注册药物的重现性方面是合理的。该方法有望用于基于组学的药物发现。
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来源期刊
Molecular Informatics
Molecular Informatics CHEMISTRY, MEDICINAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.30
自引率
2.80%
发文量
70
审稿时长
3 months
期刊介绍: Molecular Informatics is a peer-reviewed, international forum for publication of high-quality, interdisciplinary research on all molecular aspects of bio/cheminformatics and computer-assisted molecular design. Molecular Informatics succeeded QSAR & Combinatorial Science in 2010. Molecular Informatics presents methodological innovations that will lead to a deeper understanding of ligand-receptor interactions, macromolecular complexes, molecular networks, design concepts and processes that demonstrate how ideas and design concepts lead to molecules with a desired structure or function, preferably including experimental validation. The journal''s scope includes but is not limited to the fields of drug discovery and chemical biology, protein and nucleic acid engineering and design, the design of nanomolecular structures, strategies for modeling of macromolecular assemblies, molecular networks and systems, pharmaco- and chemogenomics, computer-assisted screening strategies, as well as novel technologies for the de novo design of biologically active molecules. As a unique feature Molecular Informatics publishes so-called "Methods Corner" review-type articles which feature important technological concepts and advances within the scope of the journal.
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