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Title: | Discovery of a small-molecule binder of the oncoprotein gankyrin that modulates gankyrin activity in the cell | Authors: | Chattopadhyay, A O'Connor, C.J Zhang, F Galvagnion, C Galloway, W.R.J.D Tan, Y.S Stokes, J.E Rahman, T Verma, C Spring, D.R Itzhaki, L.S |
Keywords: | antineoplastic agent AURKA protein, human aurora A kinase benzenesulfonic acid derivative cell cycle protein cjoc42 compound microtubule associated protein nuclear protein oncoprotein proteasome protein p53 PSMD10 protein, human Rad51 protein TP53 protein, human TPX2 protein, human triazole derivative calorimetry cell survival chemistry DNA damage Escherichia coli gene expression profiling gene expression regulation human mass spectrometry metabolism neoplasm nuclear magnetic resonance spectroscopy thermodynamics tumor cell line Antineoplastic Agents Aurora Kinase A Benzenesulfonates Calorimetry Cell Cycle Proteins Cell Line, Tumor Cell Survival DNA Damage Escherichia coli Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Magnetic Resonance Spectroscopy Mass Spectrometry Microtubule-Associated Proteins Neoplasms Nuclear Proteins Proteasome Endopeptidase Complex Proto-Oncogene Proteins Rad51 Recombinase Thermodynamics Triazoles Tumor Suppressor Protein p53 |
Issue Date: | 2016 | Publisher: | Nature Publishing Group | Citation: | Chattopadhyay, A, O'Connor, C.J, Zhang, F, Galvagnion, C, Galloway, W.R.J.D, Tan, Y.S, Stokes, J.E, Rahman, T, Verma, C, Spring, D.R, Itzhaki, L.S (2016). Discovery of a small-molecule binder of the oncoprotein gankyrin that modulates gankyrin activity in the cell. Scientific Reports 6 : 23732. ScholarBank@NUS Repository. https://doi.org/10.1038/srep23732 | Rights: | Attribution 4.0 International | Abstract: | Gankyrin is an ankyrin-repeat oncoprotein whose overexpression has been implicated in the development of many cancer types. Elevated gankyrin levels are linked to aberrant cellular events including enhanced degradation of tumour suppressor protein p53, and inhibition of gankyrin activity has therefore been identified as an attractive anticancer strategy. Gankyrin interacts with several partner proteins, and a number of these protein-protein interactions (PPIs) are of relevance to cancer. Thus, molecules that bind the PPI interface of gankyrin and interrupt these interactions are of considerable interest. Herein, we report the discovery of a small molecule termed cjoc42 that is capable of binding to gankyrin. Cell-based experiments demonstrate that cjoc42 can inhibit gankyrin activity in a dose-dependent manner: cjoc42 prevents the decrease in p53 protein levels normally associated with high amounts of gankyrin, and it restores p53-dependent transcription and sensitivity to DNA damage. The results represent the first evidence that gankyrin is a "druggable" target with small molecules. | Source Title: | Scientific Reports | URI: | https://scholarbank.nus.edu.sg/handle/10635/182485 | ISSN: | 2045-2322 | DOI: | 10.1038/srep23732 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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