2014
DOI: 10.4258/hir.2014.20.1.52
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Drug Similarity Search Based on Combined Signatures in Gene Expression Profiles

Abstract: ObjectivesRecently, comparison of drug responses on gene expression has been a major approach to identifying the functional similarity of drugs. Previous studies have mostly focused on a single feature, the expression differences of individual genes. We provide a more robust and accurate method to compare the functional similarity of drugs by diversifying the features of comparison in gene expression and considering the sample dependent variations.MethodsFor differentially expressed gene measurement, we modifi… Show more

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Cited by 13 publications
(10 citation statements)
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“…Modules are considered to be stable groups in biological networks, and the module biomarkers may be robust, which are not likely to be affected by individual gene expression changes . Thus, a coexpressed module may provide more implications to infer drug actions . The CAMs and UAMs of different drugs may serve as universal or specific targets in disease treatment.…”
Section: Discussionmentioning
confidence: 99%
“…Modules are considered to be stable groups in biological networks, and the module biomarkers may be robust, which are not likely to be affected by individual gene expression changes . Thus, a coexpressed module may provide more implications to infer drug actions . The CAMs and UAMs of different drugs may serve as universal or specific targets in disease treatment.…”
Section: Discussionmentioning
confidence: 99%
“…Similarity matrices constructed on these gene expression profiles can be exploited to cluster drugs to categorize potential mechanisms of action and generate drug combination hypotheses based on the joint dissimilarity of gene expression patterns of drug pairs as compared to those associated with disease states. 1215…”
Section: Introductionmentioning
confidence: 99%
“…42 In this paper, we developed a novel method to identify drug RMs and elucidated the potential pharmacological mechanisms of different compounds individually (BA, JA or UA) and in combinations (BJ or JU) in treating cerebral ischemia-reperfusion injury. In contrast to conventional studies on drug response that mainly focused on genes and pathways, [43][44][45] our method focused on modules and analyzed both their topological structures and functions, which provided a holistic view of the overall differences and similarities in the pharmacological effects of the five compounds at a systems level. All of the compounds contained more RM D s than RM E s, indicating that several modules vanished after drug intervention.…”
Section: Discussionmentioning
confidence: 99%