Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep23732
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dc.titleDiscovery of a small-molecule binder of the oncoprotein gankyrin that modulates gankyrin activity in the cell
dc.contributor.authorChattopadhyay, A
dc.contributor.authorO'Connor, C.J
dc.contributor.authorZhang, F
dc.contributor.authorGalvagnion, C
dc.contributor.authorGalloway, W.R.J.D
dc.contributor.authorTan, Y.S
dc.contributor.authorStokes, J.E
dc.contributor.authorRahman, T
dc.contributor.authorVerma, C
dc.contributor.authorSpring, D.R
dc.contributor.authorItzhaki, L.S
dc.date.accessioned2020-10-31T11:37:08Z
dc.date.available2020-10-31T11:37:08Z
dc.date.issued2016
dc.identifier.citationChattopadhyay, 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
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/182485
dc.description.abstractGankyrin 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.
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectantineoplastic agent
dc.subjectAURKA protein, human
dc.subjectaurora A kinase
dc.subjectbenzenesulfonic acid derivative
dc.subjectcell cycle protein
dc.subjectcjoc42 compound
dc.subjectmicrotubule associated protein
dc.subjectnuclear protein
dc.subjectoncoprotein
dc.subjectproteasome
dc.subjectprotein p53
dc.subjectPSMD10 protein, human
dc.subjectRad51 protein
dc.subjectTP53 protein, human
dc.subjectTPX2 protein, human
dc.subjecttriazole derivative
dc.subjectcalorimetry
dc.subjectcell survival
dc.subjectchemistry
dc.subjectDNA damage
dc.subjectEscherichia coli
dc.subjectgene expression profiling
dc.subjectgene expression regulation
dc.subjecthuman
dc.subjectmass spectrometry
dc.subjectmetabolism
dc.subjectneoplasm
dc.subjectnuclear magnetic resonance spectroscopy
dc.subjectthermodynamics
dc.subjecttumor cell line
dc.subjectAntineoplastic Agents
dc.subjectAurora Kinase A
dc.subjectBenzenesulfonates
dc.subjectCalorimetry
dc.subjectCell Cycle Proteins
dc.subjectCell Line, Tumor
dc.subjectCell Survival
dc.subjectDNA Damage
dc.subjectEscherichia coli
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMagnetic Resonance Spectroscopy
dc.subjectMass Spectrometry
dc.subjectMicrotubule-Associated Proteins
dc.subjectNeoplasms
dc.subjectNuclear Proteins
dc.subjectProteasome Endopeptidase Complex
dc.subjectProto-Oncogene Proteins
dc.subjectRad51 Recombinase
dc.subjectThermodynamics
dc.subjectTriazoles
dc.subjectTumor Suppressor Protein p53
dc.typeArticle
dc.contributor.departmentBIOLOGY (NU)
dc.description.doi10.1038/srep23732
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page23732
dc.published.statepublished
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