Using Functional Signature Ontology (FUSION) to Identify Mechanisms of Action for Natural Products
Year: 2013
Type: article
Abstract: A challenge for biomedical research is the development of pharmaceuticals that appropriately target disease mechanisms. Natural products can be a rich source of bioactive chemicals for medicinal applications but can act through unknown mechanisms and can be difficult to produce or obtain. To address these challenges, we developed a new marine-derived, renewable natural products resource and a method for linking bioactive derivatives of this library to the proteins and biological processes that they target in cells. We used cell-based screening and computational analysis to match gene expression signatures produced by natural products to those produced by small interfering RNA (siRNA) and synthetic microRNA (miRNA) libraries. With this strategy, we matched proteins and miRNAs with diverse biological processes and also identified putative protein targets and mechanisms of action for several previously undescribed marine-derived natural products. We confirmed mechanistic relationships for selected siRNAs, miRNAs, and compounds with functional roles in autophagy, chemotaxis mediated by discoidin domain receptor 2, or activation of the kinase AKT. Thus, this approach may be an effective method for screening new drugs while simultaneously identifying their targets.
Source: Science Signaling
Authors: Malia B. Potts, Hyun Seok Kim, Kurt W. Fisher, Youcai Hu, Yazmin P. Carrasco, Gamze Betul Bulut, Yi-Hung Ou, Mireya L. Herrera-Herrera, Federico Cubillos, Saurabh Mendiratta, Guanghua Xiao, Matan Hofree, Trey Ideker, Yang Xie, Lily Jun-shen Huang, Robert E. Lewis, John B. MacMillan, Michael A. White
Language: English
Subfield: Computational Theory and Mathematics
Field: Computer Science
Domain: Physical Sciences
Open Access status: green
Awards: G1592772826, The RaLGTPase Regulatory Network, Marine Actinomycetes as a Resource for Anticancer Natural Products, G2782664826, G3731018441, Predicting Adjuvant Chemotherapy Response in Lung Cancer, Components of Ras-mediated growth control, G4225004395, National Resource for Network Biology (NRNB), KSR, a Modifier of Ras-Mediated Cell Transformation, Lung cancer oncogenotype-selective drug target discovery, Cancer Biology Training Grant, G7296110585, Novel Effectors of Colon Tumorigenesis, G8537961454, UT Southwestern Medical Center Simmons Comprehensive Cancer Center, Buffett Cancer Center Support Grant
OpenAlex ID: W2063890235
