Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep23732
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

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1038_srep23732.pdf2.68 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons