Publications by authors named "Changhe Fu"

Article Synopsis
  • The study aims to improve how biological pathways are inferred by integrating genetic and protein interaction data, addressing limitations in existing models like activity pathway networks (APN).
  • Researchers created a new method using probabilistic graphical models, specifically Bayesian networks, to better reconstruct detailed pathway structures from these interactions, successfully identifying known cellular pathways.
  • The new method outperforms APN by accurately resolving ambiguities in pathway connections and utilizing a simplified scoring function based solely on genetic interactions, demonstrating enhanced performance through effective algorithms.
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Identification of oncogenic genes from a large sample number of genomic data is a challenge. In this study, a well-established latent factor model, Bayesian factor and regression model, are applied to predict unknown colon cancer related genes from colon adenocarcinoma genomic data. Four important latent factors were addressed by the latent factor model, focusing on characterisation of heterogeneity of expression patterns of specific oncogenic genes by using microarray data of 174 colon cancer patients.

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Summary: Systematic studies of drug repositioning require the integration of multi-level drug data, including basic chemical information (such as SMILES), drug targets, target-related signaling pathways, clinical trial information and Food and Drug Administration (FDA)-approval information, to predict new potential indications of existing drugs. Currently available databases, however, lack query support for multi-level drug information and thus are not designed to support drug repositioning studies. DrugMap Central (DMC), an online tool, is developed to help fill the gap.

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Little research has been done to address the huge opportunities that may exist to reposition existing approved or generic drugs for alternate uses in cancer therapy. In addition, there has been little work on strategies to reposition experimental cancer agents for testing in alternate settings that could shorten their clinical development time. Progress in each area has lagged, in part, because of the lack of systematic methods to define drug off-target effects (OTE) that might affect important cancer cell signaling pathways.

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